|Other names||HIV disease, HIV infection|
|The red ribbon is a symbol for solidarity with HIV-positive people and those living with AIDS.|
|Specialty||Infectious disease, immunology|
|Symptoms||Early: Flu-like illness|
Later: Large lymph nodes, fever, weight loss
|Complications||Opportunistic infections, tumors|
|Causes||Human immunodeficiency virus (HIV)|
|Risk factors||Unprotected anal or vaginal sex, having another sexually transmitted infection, needle sharing, medical procedures involving unsterile cutting or piercing, and experiencing needlestick injury|
|Diagnostic method||Blood tests|
|Prevention||Safe sex, needle exchange, male circumcision, pre-exposure prophylaxis, post-exposure prophylaxis|
|Prognosis||Near normal life expectancy with treatment|
11 years life expectancy without treatment
|Frequency||64.4 million – 113 million total cases|
1.5 million new cases (2021)
38.4 million living with HIV (2021)
|Deaths||40.1 million total deaths|
Human immunodeficiency virus infection and acquired immunodeficiency syndrome (HIV/AIDS) is a spectrum of conditions caused by infection with the human immunodeficiency virus (HIV), a retrovirus. Following initial infection an individual may not notice any symptoms, or may experience a brief period of influenza-like illness. Typically, this is followed by a prolonged incubation period with no symptoms. If the infection progresses, it interferes more with the immune system, increasing the risk of developing common infections such as tuberculosis, as well as other opportunistic infections, and tumors which are rare in people who have normal immune function. These late symptoms of infection are referred to as acquired immunodeficiency syndrome (AIDS). This stage is often also associated with unintended weight loss.
HIV is spread primarily by unprotected sex (including anal and vaginal sex), contaminated hypodermic needles or blood transfusions, and from mother to child during pregnancy, delivery, or breastfeeding. Some bodily fluids, such as saliva, sweat and tears, do not transmit the virus. Oral sex has little to no risk of transmitting the virus. Methods of prevention include safe sex, needle exchange programs, treating those who are infected, as well as both pre- and post-exposure prophylaxis. Disease in a baby can often be prevented by giving both the mother and child antiretroviral medication.
Recognized worldwide in the early 1980s, HIV/AIDS has had a large impact on society, both as an illness and as a source of discrimination. The disease also has large economic impacts. There are many misconceptions about HIV/AIDS, such as the belief that it can be transmitted by casual non-sexual contact. The disease has become subject to many controversies involving religion, including the Catholic Church's position not to support condom use as prevention. It has attracted international medical and political attention as well as large-scale funding since it was identified in the 1980s.
HIV made the jump from other primates to humans in west-central Africa in the early-to-mid 20th century. AIDS was first recognized by the U.S. Centers for Disease Control and Prevention (CDC) in 1981 and its cause—HIV infection—was identified in the early part of the decade. Between the first time AIDS was readily identified through 2021, the disease is estimated to have caused at least 40 million deaths worldwide. In 2021, there were 650,000 deaths and about 38 million people worldwide living with HIV. An estimated 20.6 million of these people live in eastern and southern Africa. HIV/AIDS is considered a pandemic—a disease outbreak which is present over a large area and is actively spreading.
The United States' National Institutes of Health (NIH) and the Gates Foundation have pledged $200 million focused on developing a global cure for AIDS. While there is no cure or vaccine, antiretroviral treatment can slow the course of the disease and may lead to a near-normal life expectancy. Treatment is recommended as soon as the diagnosis is made. Without treatment, the average survival time after infection is 11 years.
Signs and symptoms
There are three main stages of HIV infection: acute infection, clinical latency, and AIDS.
The initial period following the contraction of HIV is called acute HIV, primary HIV or acute retroviral syndrome. Many individuals develop an influenza-like illness or a mononucleosis-like illness 2–4 weeks after exposure while others have no significant symptoms. Symptoms occur in 40–90% of cases and most commonly include fever, large tender lymph nodes, throat inflammation, a rash, headache, tiredness, and/or sores of the mouth and genitals. The rash, which occurs in 20–50% of cases, presents itself on the trunk and is maculopapular, classically. Some people also develop opportunistic infections at this stage. Gastrointestinal symptoms, such as vomiting or diarrhea may occur. Neurological symptoms of peripheral neuropathy or Guillain–Barré syndrome also occur. The duration of the symptoms varies, but is usually one or two weeks.
Owing to their nonspecific character, these symptoms are not often recognized as signs of HIV infection. Even cases that do get seen by a family doctor or a hospital are often misdiagnosed as one of the many common infectious diseases with overlapping symptoms. Thus, it is recommended that HIV be considered in people presenting with an unexplained fever who may have risk factors for the infection.
The initial symptoms are followed by a stage called clinical latency, asymptomatic HIV, or chronic HIV. Without treatment, this second stage of the natural history of HIV infection can last from about three years to over 20 years (on average, about eight years). While typically there are few or no symptoms at first, near the end of this stage many people experience fever, weight loss, gastrointestinal problems and muscle pains. Between 50% and 70% of people also develop persistent generalized lymphadenopathy, characterized by unexplained, non-painful enlargement of more than one group of lymph nodes (other than in the groin) for over three to six months.
Although most HIV-1 infected individuals have a detectable viral load and in the absence of treatment will eventually progress to AIDS, a small proportion (about 5%) retain high levels of CD4+ T cells (T helper cells) without antiretroviral therapy for more than five years. These individuals are classified as "HIV controllers" or long-term nonprogressors (LTNP). Another group consists of those who maintain a low or undetectable viral load without anti-retroviral treatment, known as "elite controllers" or "elite suppressors". They represent approximately 1 in 300 infected persons.
Acquired immunodeficiency syndrome
Acquired immunodeficiency syndrome (AIDS) is defined as an HIV infection with either a CD4+ T cell count below 200 cells per µL or the occurrence of specific diseases associated with HIV infection. In the absence of specific treatment, around half of people infected with HIV develop AIDS within ten years. The most common initial conditions that alert to the presence of AIDS are pneumocystis pneumonia (40%), cachexia in the form of HIV wasting syndrome (20%), and esophageal candidiasis. Other common signs include recurrent respiratory tract infections.
Opportunistic infections may be caused by bacteria, viruses, fungi, and parasites that are normally controlled by the immune system. Which infections occur depends partly on what organisms are common in the person's environment. These infections may affect nearly every organ system.
People with AIDS have an increased risk of developing various viral-induced cancers, including Kaposi's sarcoma, Burkitt's lymphoma, primary central nervous system lymphoma, and cervical cancer. Kaposi's sarcoma is the most common cancer, occurring in 10% to 20% of people with HIV. The second-most common cancer is lymphoma, which is the cause of death of nearly 16% of people with AIDS and is the initial sign of AIDS in 3% to 4%. Both these cancers are associated with human herpesvirus 8 (HHV-8). Cervical cancer occurs more frequently in those with AIDS because of its association with human papillomavirus (HPV). Conjunctival cancer (of the layer that lines the inner part of eyelids and the white part of the eye) is also more common in those with HIV.
Additionally, people with AIDS frequently have systemic symptoms such as prolonged fevers, sweats (particularly at night), swollen lymph nodes, chills, weakness, and unintended weight loss. Diarrhea is another common symptom, present in about 90% of people with AIDS. They can also be affected by diverse psychiatric and neurological symptoms independent of opportunistic infections and cancers.
|Exposure route||Chance of infection|
|Childbirth (to child)||25%[clarification needed]|
|Needle-sharing injection drug use||0.67%|
|Percutaneous needle stick||0.30%|
|Receptive anal intercourse*||0.04–3.0%|
|Insertive anal intercourse*||0.03%|
|Receptive penile-vaginal intercourse*||0.05–0.30%|
|Insertive penile-vaginal intercourse*||0.01–0.38%|
|Receptive oral intercourse*§||0–0.04%|
|Insertive oral intercourse*§||0–0.005%|
|* assuming no condom use |
§ source refers to oral intercourse
performed on a man
HIV is spread by three main routes: sexual contact, significant exposure to infected body fluids or tissues, and from mother to child during pregnancy, delivery, or breastfeeding (known as vertical transmission). There is no risk of acquiring HIV if exposed to feces, nasal secretions, saliva, sputum, sweat, tears, urine, or vomit unless these are contaminated with blood. It is also possible to be co-infected by more than one strain of HIV—a condition known as HIV superinfection.
The most frequent mode of transmission of HIV is through sexual contact with an infected person. However, an HIV-positive person who has an undetectable viral load as a result of long-term treatment has effectively no risk of transmitting HIV sexually. The existence of functionally noncontagious HIV-positive people on antiretroviral therapy was controversially publicized in the 2008 Swiss Statement, and has since become accepted as medically sound.
Globally, the most common mode of HIV transmission is via sexual contacts between people of the opposite sex; however, the pattern of transmission varies among countries. As of 2017[update], most HIV transmission in the United States occurred among men who had sex with men (82% of new HIV diagnoses among males aged 13 and older and 70% of total new diagnoses). In the US, gay and bisexual men aged 13 to 24 accounted for an estimated 92% of new HIV diagnoses among all men in their age group and 27% of new diagnoses among all gay and bisexual men.
With regard to unprotected heterosexual contacts, estimates of the risk of HIV transmission per sexual act appear to be four to ten times higher in low-income countries than in high-income countries. In low-income countries, the risk of female-to-male transmission is estimated as 0.38% per act, and of male-to-female transmission as 0.30% per act; the equivalent estimates for high-income countries are 0.04% per act for female-to-male transmission, and 0.08% per act for male-to-female transmission. The risk of transmission from anal intercourse is especially high, estimated as 1.4–1.7% per act in both heterosexual and homosexual contacts. While the risk of transmission from oral sex is relatively low, it is still present. The risk from receiving oral sex has been described as "nearly nil"; however, a few cases have been reported. The per-act risk is estimated at 0–0.04% for receptive oral intercourse. In settings involving prostitution in low-income countries, risk of female-to-male transmission has been estimated as 2.4% per act, and of male-to-female transmission as 0.05% per act.
Risk of transmission increases in the presence of many sexually transmitted infections and genital ulcers. Genital ulcers appear to increase the risk approximately fivefold. Other sexually transmitted infections, such as gonorrhea, chlamydia, trichomoniasis, and bacterial vaginosis, are associated with somewhat smaller increases in risk of transmission.
The viral load of an infected person is an important risk factor in both sexual and mother-to-child transmission. During the first 2.5 months of an HIV infection a person's infectiousness is twelve times higher due to the high viral load associated with acute HIV. If the person is in the late stages of infection, rates of transmission are approximately eightfold greater.
Commercial sex workers (including those in pornography) have an increased likelihood of contracting HIV. Rough sex can be a factor associated with an increased risk of transmission. Sexual assault is also believed to carry an increased risk of HIV transmission as condoms are rarely worn, physical trauma to the vagina or rectum is likely, and there may be a greater risk of concurrent sexually transmitted infections.
The second-most frequent mode of HIV transmission is via blood and blood products. Blood-borne transmission can be through needle-sharing during intravenous drug use, needle-stick injury, transfusion of contaminated blood or blood product, or medical injections with unsterilized equipment. The risk from sharing a needle during drug injection is between 0.63% and 2.4% per act, with an average of 0.8%. The risk of acquiring HIV from a needle stick from an HIV-infected person is estimated as 0.3% (about 1 in 333) per act and the risk following mucous membrane exposure to infected blood as 0.09% (about 1 in 1000) per act. This risk may, however, be up to 5% if the introduced blood was from a person with a high viral load and the cut was deep. In the United States, intravenous drug users made up 12% of all new cases of HIV in 2009, and in some areas more than 80% of people who inject drugs are HIV-positive.
HIV is transmitted in about 90% of blood transfusions using infected blood. In developed countries the risk of acquiring HIV from a blood transfusion is extremely low (less than one in half a million) where improved donor selection and HIV screening is performed; for example, in the UK the risk is reported at one in five million and in the United States it was one in 1.5 million in 2008. In low-income countries, only half of transfusions may be appropriately screened (as of 2008), and it is estimated that up to 15% of HIV infections in these areas come from transfusion of infected blood and blood products, representing between 5% and 10% of global infections. It is possible to acquire HIV from organ and tissue transplantation, although this is rare because of screening.
Unsafe medical injections play a role in HIV spread in sub-Saharan Africa. In 2007, between 12% and 17% of infections in this region were attributed to medical syringe use. The World Health Organization estimates the risk of transmission as a result of a medical injection in Africa at 1.2%. Risks are also associated with invasive procedures, assisted delivery, and dental care in this area of the world.
People giving or receiving tattoos, piercings, and scarification are theoretically at risk of infection but no confirmed cases have been documented. It is not possible for mosquitoes or other insects to transmit HIV.
HIV can be transmitted from mother to child during pregnancy, during delivery, or through breast milk, resulting in the baby also contracting HIV. As of 2008, vertical transmission accounted for about 90% of cases of HIV in children. In the absence of treatment, the risk of transmission before or during birth is around 20%, and in those who also breastfeed 35%. Treatment decreases this risk to less than 5%.
Antiretrovirals when taken by either the mother or the baby decrease the risk of transmission in those who do breastfeed. If blood contaminates food during pre-chewing it may pose a risk of transmission. If a woman is untreated, two years of breastfeeding results in an HIV/AIDS risk in her baby of about 17%. Due to the increased risk of death without breastfeeding in many areas in the developing world, the World Health Organization recommends either exclusive breastfeeding or the provision of safe formula. All women known to be HIV-positive should be taking lifelong antiretroviral therapy.
HIV is the cause of the spectrum of disease known as HIV/AIDS. HIV is a retrovirus that primarily infects components of the human immune system such as CD4+ T cells, macrophages and dendritic cells. It directly and indirectly destroys CD4+ T cells.
HIV is a member of the genus Lentivirus, part of the family Retroviridae. Lentiviruses share many morphological and biological characteristics. Many species of mammals are infected by lentiviruses, which are characteristically responsible for long-duration illnesses with a long incubation period. Lentiviruses are transmitted as single-stranded, positive-sense, enveloped RNA viruses. Upon entry into the target cell, the viral RNA genome is converted (reverse transcribed) into double-stranded DNA by a virally encoded reverse transcriptase that is transported along with the viral genome in the virus particle. The resulting viral DNA is then imported into the cell nucleus and integrated into the cellular DNA by a virally encoded integrase and host co-factors. Once integrated, the virus may become latent, allowing the virus and its host cell to avoid detection by the immune system. Alternatively, the virus may be transcribed, producing new RNA genomes and viral proteins that are packaged and released from the cell as new virus particles that begin the replication cycle anew.
HIV is now known to spread between CD4+ T cells by two parallel routes: cell-free spread and cell-to-cell spread, i.e. it employs hybrid spreading mechanisms. In the cell-free spread, virus particles bud from an infected T cell, enter the blood/extracellular fluid and then infect another T cell following a chance encounter. HIV can also disseminate by direct transmission from one cell to another by a process of cell-to-cell spread. The hybrid spreading mechanisms of HIV contribute to the virus's ongoing replication against antiretroviral therapies.
Two types of HIV have been characterized: HIV-1 and HIV-2. HIV-1 is the virus that was originally discovered (and initially referred to also as LAV or HTLV-III). It is more virulent, more infective, and is the cause of the majority of HIV infections globally. The lower infectivity of HIV-2 as compared with HIV-1 implies that fewer people exposed to HIV-2 will be infected per exposure. Because of its relatively poor capacity for transmission, HIV-2 is largely confined to West Africa.
After the virus enters the body, there is a period of rapid viral replication, leading to an abundance of virus in the peripheral blood. During primary infection, the level of HIV may reach several million virus particles per milliliter of blood. This response is accompanied by a marked drop in the number of circulating CD4+ T cells. The acute viremia is almost invariably associated with activation of CD8+ T cells, which kill HIV-infected cells, and subsequently with antibody production, or seroconversion. The CD8+ T cell response is thought to be important in controlling virus levels, which peak and then decline, as the CD4+ T cell counts recover. A good CD8+ T cell response has been linked to slower disease progression and a better prognosis, though it does not eliminate the virus.
Ultimately, HIV causes AIDS by depleting CD4+ T cells. This weakens the immune system and allows opportunistic infections. T cells are essential to the immune response and without them, the body cannot fight infections or kill cancerous cells. The mechanism of CD4+ T cell depletion differs in the acute and chronic phases. During the acute phase, HIV-induced cell lysis and killing of infected cells by CD8+ T cells accounts for CD4+ T cell depletion, although apoptosis may also be a factor. During the chronic phase, the consequences of generalized immune activation coupled with the gradual loss of the ability of the immune system to generate new T cells appear to account for the slow decline in CD4+ T cell numbers.
Although the symptoms of immune deficiency characteristic of AIDS do not appear for years after a person is infected, the bulk of CD4+ T cell loss occurs during the first weeks of infection, especially in the intestinal mucosa, which harbors the majority of the lymphocytes found in the body. The reason for the preferential loss of mucosal CD4+ T cells is that the majority of mucosal CD4+ T cells express the CCR5 protein which HIV uses as a co-receptor to gain access to the cells, whereas only a small fraction of CD4+ T cells in the bloodstream do so. A specific genetic change that alters the CCR5 protein when present in both chromosomes very effectively prevents HIV-1 infection.
HIV seeks out and destroys CCR5 expressing CD4+ T cells during acute infection. A vigorous immune response eventually controls the infection and initiates the clinically latent phase. CD4+ T cells in mucosal tissues remain particularly affected. Continuous HIV replication causes a state of generalized immune activation persisting throughout the chronic phase. Immune activation, which is reflected by the increased activation state of immune cells and release of pro-inflammatory cytokines, results from the activity of several HIV gene products and the immune response to ongoing HIV replication. It is also linked to the breakdown of the immune surveillance system of the gastrointestinal mucosal barrier caused by the depletion of mucosal CD4+ T cells during the acute phase of disease.
|Antibody test (rapid test, ELISA 3rd gen)||23–90|
|Antibody and p24 antigen test (ELISA 4th gen)||18–45|
HIV/AIDS is diagnosed via laboratory testing and then staged based on the presence of certain signs or symptoms. HIV screening is recommended by the United States Preventive Services Task Force for all people 15 years to 65 years of age, including all pregnant women. Additionally, testing is recommended for those at high risk, which includes anyone diagnosed with a sexually transmitted illness. In many areas of the world, a third of HIV carriers only discover they are infected at an advanced stage of the disease when AIDS or severe immunodeficiency has become apparent.
Most people infected with HIV develop specific antibodies (i.e. seroconvert) within three to twelve weeks after the initial infection. Diagnosis of primary HIV before seroconversion is done by measuring HIV-RNA or p24 antigen. Positive results obtained by antibody or PCR testing are confirmed either by a different antibody or by PCR.
Antibody tests in children younger than 18 months are typically inaccurate, due to the continued presence of maternal antibodies. Thus HIV infection can only be diagnosed by PCR testing for HIV RNA or DNA, or via testing for the p24 antigen. Much of the world lacks access to reliable PCR testing, and people in many places simply wait until either symptoms develop or the child is old enough for accurate antibody testing. In sub-Saharan Africa between 2007 and 2009, between 30% and 70% of the population were aware of their HIV status. In 2009, between 3.6% and 42% of men and women in sub-Saharan countries were tested; this represented a significant increase compared to previous years.
Two main clinical staging systems are used to classify HIV and HIV-related disease for surveillance purposes: the WHO disease staging system for HIV infection and disease, and the CDC classification system for HIV infection. The CDC's classification system is more frequently adopted in developed countries. Since the WHO's staging system does not require laboratory tests, it is suited to the resource-restricted conditions encountered in developing countries, where it can also be used to help guide clinical management. Despite their differences, the two systems allow a comparison for statistical purposes.
The World Health Organization first proposed a definition for AIDS in 1986. Since then, the WHO classification has been updated and expanded several times, with the most recent version being published in 2007. The WHO system uses the following categories:
- Primary HIV infection: May be either asymptomatic or associated with acute retroviral syndrome
- Stage I: HIV infection is asymptomatic with a CD4+ T cell count (also known as CD4 count) greater than 500 per microlitre (µl or cubic mm) of blood. May include generalized lymph node enlargement.
- Stage II: Mild symptoms, which may include minor mucocutaneous manifestations and recurrent upper respiratory tract infections. A CD4 count of less than 500/µl
- Stage III: Advanced symptoms, which may include unexplained chronic diarrhea for longer than a month, severe bacterial infections including tuberculosis of the lung, and a CD4 count of less than 350/µl
- Stage IV or AIDS: severe symptoms, which include toxoplasmosis of the brain, candidiasis of the esophagus, trachea, bronchi, or lungs, and Kaposi's sarcoma. A CD4 count of less than 200/µl
The U.S. Centers for Disease Control and Prevention also created a classification system for HIV, and updated it in 2008 and 2014. This system classifies HIV infections based on CD4 count and clinical symptoms, and describes the infection in five groups. In those greater than six years of age it is:
- Stage 0: the time between a negative or indeterminate HIV test followed less than 180 days by a positive test.
- Stage 1: CD4 count ≥ 500 cells/µl and no AIDS-defining conditions.
- Stage 2: CD4 count 200 to 500 cells/µl and no AIDS-defining conditions.
- Stage 3: CD4 count ≤ 200 cells/µl or AIDS-defining conditions.
- Unknown: if insufficient information is available to make any of the above classifications.
For surveillance purposes, the AIDS diagnosis still stands even if, after treatment, the CD4+ T cell count rises to above 200 per µL of blood or other AIDS-defining illnesses are cured.
Consistent condom use reduces the risk of HIV transmission by approximately 80% over the long term. When condoms are used consistently by a couple in which one person is infected, the rate of HIV infection is less than 1% per year. There is some evidence to suggest that female condoms may provide an equivalent level of protection. Application of a vaginal gel containing tenofovir (a reverse transcriptase inhibitor) immediately before sex seems to reduce infection rates by approximately 40% among African women. By contrast, use of the spermicide nonoxynol-9 may increase the risk of transmission due to its tendency to cause vaginal and rectal irritation.
Circumcision in sub-Saharan Africa "reduces the acquisition of HIV by heterosexual men by between 38% and 66% over 24 months". Owing to these studies, both the World Health Organization and UNAIDS recommended male circumcision in 2007 as a method of preventing female-to-male HIV transmission in areas with high rates of HIV. However, whether it protects against male-to-female transmission is disputed, and whether it is of benefit in developed countries and among men who have sex with men is undetermined.
Programs encouraging sexual abstinence do not appear to affect subsequent HIV risk. Evidence of any benefit from peer education is equally poor. Comprehensive sexual education provided at school may decrease high-risk behavior. A substantial minority of young people continues to engage in high-risk practices despite knowing about HIV/AIDS, underestimating their own risk of becoming infected with HIV. Voluntary counseling and testing people for HIV does not affect risky behavior in those who test negative but does increase condom use in those who test positive. Enhanced family planning services appear to increase the likelihood of women with HIV using contraception, compared to basic services. It is not known whether treating other sexually transmitted infections is effective in preventing HIV.
Antiretroviral treatment among people with HIV whose CD4 count ≤ 550 cells/µL is a very effective way to prevent HIV infection of their partner (a strategy known as treatment as prevention, or TASP). TASP is associated with a 10- to 20-fold reduction in transmission risk. Pre-exposure prophylaxis (PrEP) with a daily dose of the medications tenofovir, with or without emtricitabine, is effective in people at high risk including men who have sex with men, couples where one is HIV-positive, and young heterosexuals in Africa. It may also be effective in intravenous drug users, with a study finding a decrease in risk of 0.7 to 0.4 per 100 person years. The USPSTF, in 2019, recommended PrEP in those who are at high risk.
Universal precautions within the health care environment are believed to be effective in decreasing the risk of HIV. Intravenous drug use is an important risk factor, and harm reduction strategies such as needle-exchange programs and opioid substitution therapy appear effective in decreasing this risk.
A course of antiretrovirals administered within 48 to 72 hours after exposure to HIV-positive blood or genital secretions is referred to as post-exposure prophylaxis (PEP). The use of the single agent zidovudine reduces the risk of a HIV infection five-fold following a needle-stick injury. As of 2013[update], the prevention regimen recommended in the United States consists of three medications—tenofovir, emtricitabine and raltegravir—as this may reduce the risk further.
PEP treatment is recommended after a sexual assault when the perpetrator is known to be HIV-positive, but is controversial when their HIV status is unknown. The duration of treatment is usually four weeks and is frequently associated with adverse effects—where zidovudine is used, about 70% of cases result in adverse effects such as nausea (24%), fatigue (22%), emotional distress (13%) and headaches (9%).
Programs to prevent the vertical transmission of HIV (from mothers to children) can reduce rates of transmission by 92–99%. This primarily involves the use of a combination of antiviral medications during pregnancy and after birth in the infant, and potentially includes bottle feeding rather than breastfeeding. If replacement feeding is acceptable, feasible, affordable, sustainable and safe, mothers should avoid breastfeeding their infants; however, exclusive breastfeeding is recommended during the first months of life if this is not the case. If exclusive breastfeeding is carried out, the provision of extended antiretroviral prophylaxis to the infant decreases the risk of transmission. In 2015, Cuba became the first country in the world to eradicate mother-to-child transmission of HIV.
Currently there is no licensed vaccine for HIV or AIDS. The most effective vaccine trial to date, RV 144, was published in 2009; it found a partial reduction in the risk of transmission of roughly 30%, stimulating some hope in the research community of developing a truly effective vaccine.
There is currently no cure, nor an effective HIV vaccine. Treatment consists of highly active antiretroviral therapy (HAART), which slows progression of the disease. As of 2010[update], more than 6.6 million people were receiving HAART in low- and middle-income countries. Treatment also includes preventive and active treatment of opportunistic infections. As of July 2022[update], four people have been successfully cleared of HIV. Rapid initiation of antiretroviral therapy within one week of diagnosis appear to improve treatment outcomes in low and medium-income settings.
Current HAART options are combinations (or "cocktails") consisting of at least three medications belonging to at least two types, or "classes", of antiretroviral agents. Initially, treatment is typically a non-nucleoside reverse transcriptase inhibitor (NNRTI) plus two nucleoside analog reverse transcriptase inhibitors (NRTIs). Typical NRTIs include: zidovudine (AZT) or tenofovir (TDF) and lamivudine (3TC) or emtricitabine (FTC). As of 2019[update], dolutegravir/lamivudine/tenofovir is listed by the World Health Organization as the first-line treatment for adults, with tenofovir/lamivudine/efavirenz as an alternative. Combinations of agents that include protease inhibitors (PI) are used if the above regimen loses effectiveness.
The World Health Organization and the United States recommend antiretrovirals in people of all ages (including pregnant women) as soon as the diagnosis is made, regardless of CD4 count. Once treatment is begun, it is recommended that it is continued without breaks or "holidays". Many people are diagnosed only after treatment ideally should have begun. The desired outcome of treatment is a long-term plasma HIV-RNA count below 50 copies/mL. Levels to determine if treatment is effective are initially recommended after four weeks and once levels fall below 50 copies/mL checks every three to six months are typically adequate. Inadequate control is deemed to be greater than 400 copies/mL. Based on these criteria treatment is effective in more than 95% of people during the first year.
Benefits of treatment include a decreased risk of progression to AIDS and a decreased risk of death. In the developing world, treatment also improves physical and mental health. With treatment, there is a 70% reduced risk of acquiring tuberculosis. Additional benefits include a decreased risk of transmission of the disease to sexual partners and a decrease in mother-to-child transmission. The effectiveness of treatment depends to a large part on compliance. Reasons for non-adherence to treatment include poor access to medical care, inadequate social supports, mental illness and drug abuse. The complexity of treatment regimens (due to pill numbers and dosing frequency) and adverse effects may reduce adherence. Even though cost is an important issue with some medications, 47% of those who needed them were taking them in low- and middle-income countries as of 2010[update], and the rate of adherence is similar in low-income and high-income countries.
Specific adverse events are related to the antiretroviral agent taken. Some relatively common adverse events include: lipodystrophy syndrome, dyslipidemia, and diabetes mellitus, especially with protease inhibitors. Other common symptoms include diarrhea, and an increased risk of cardiovascular disease. Newer recommended treatments are associated with fewer adverse effects. Certain medications may be associated with birth defects and therefore may be unsuitable for women hoping to have children.
Treatment recommendations for children are somewhat different from those for adults. The World Health Organization recommends treating all children less than five years of age; children above five are treated like adults. The United States guidelines recommend treating all children less than 12 months of age and all those with HIV RNA counts greater than 100,000 copies/mL between one year and five years of age.
The European Medicines Agency (EMA) has recommended the granting of marketing authorizations for two new antiretroviral (ARV) medicines, rilpivirine (Rekambys) and cabotegravir (Vocabria), to be used together for the treatment of people with human immunodeficiency virus type 1 (HIV-1) infection. The two medicines are the first ARVs that come in a long-acting injectable formulation. This means that instead of daily pills, people receive intramuscular injections monthly or every two months.
The combination of Rekambys and Vocabria injection is intended for maintenance treatment of adults who have undetectable HIV levels in the blood (viral load less than 50 copies/ml) with their current ARV treatment, and when the virus has not developed resistance to a certain class of anti-HIV medicines called non-nucleoside reverse transcriptase inhibitors (NNRTIs) and integrase strand transfer inhibitors (INIs).
Cabotegravir combined with rilpivirine (Cabenuva) is a complete regimen for the treatment of human immunodeficiency virus type 1 (HIV-1) infection in adults to replace a current antiretroviral regimen in those who are virologically suppressed on a stable antiretroviral regimen with no history of treatment failure and with no known or suspected resistance to either cabotegravir or rilpivirine.
Measures to prevent opportunistic infections are effective in many people with HIV/AIDS. In addition to improving current disease, treatment with antiretrovirals reduces the risk of developing additional opportunistic infections.
Adults and adolescents who are living with HIV (even on anti-retroviral therapy) with no evidence of active tuberculosis in settings with high tuberculosis burden should receive isoniazid preventive therapy (IPT); the tuberculin skin test can be used to help decide if IPT is needed. Children with HIV may benefit from screening for tuberculosis. Vaccination against hepatitis A and B is advised for all people at risk of HIV before they become infected; however, it may also be given after infection.
Trimethoprim/sulfamethoxazole prophylaxis between four and six weeks of age, and ceasing breastfeeding of infants born to HIV-positive mothers, is recommended in resource-limited settings. It is also recommended to prevent PCP when a person's CD4 count is below 200 cells/uL and in those who have or have previously had PCP. People with substantial immunosuppression are also advised to receive prophylactic therapy for toxoplasmosis and MAC. Appropriate preventive measures reduced the rate of these infections by 50% between 1992 and 1997. Influenza vaccination and pneumococcal polysaccharide vaccine are often recommended in people with HIV/AIDS with some evidence of benefit.
The World Health Organization (WHO) has issued recommendations regarding nutrient requirements in HIV/AIDS. A generally healthy diet is promoted. Dietary intake of micronutrients at RDA levels by HIV-infected adults is recommended by the WHO; higher intake of vitamin A, zinc, and iron can produce adverse effects in HIV-positive adults, and is not recommended unless there is documented deficiency. Dietary supplementation for people who are infected with HIV and who have inadequate nutrition or dietary deficiencies may strengthen their immune systems or help them recover from infections; however, evidence indicating an overall benefit in morbidity or reduction in mortality is not consistent.
People with HIV/AIDS are up to four times more likely to develop type 2 diabetes than those who are not tested positive with the virus.
Evidence for supplementation with selenium is mixed with some tentative evidence of benefit. For pregnant and lactating women with HIV, multivitamin supplement improves outcomes for both mothers and children. If the pregnant or lactating mother has been advised to take anti-retroviral medication to prevent mother-to-child HIV transmission, multivitamin supplements should not replace these treatments. There is some evidence that vitamin A supplementation in children with an HIV infection reduces mortality and improves growth.
In the US, approximately 60% of people with HIV use various forms of complementary or alternative medicine, whose effectiveness has not been established. There is not enough evidence to support the use of herbal medicines. There is insufficient evidence to recommend or support the use of medical cannabis to try to increase appetite or weight gain.
HIV/AIDS has become a chronic rather than an acutely fatal disease in many areas of the world. Prognosis varies between people, and both the CD4 count and viral load are useful for predicted outcomes. Without treatment, average survival time after infection with HIV is estimated to be 9 to 11 years, depending on the HIV subtype. After the diagnosis of AIDS, if treatment is not available, survival ranges between 6 and 19 months. HAART and appropriate prevention of opportunistic infections reduces the death rate by 80%, and raises the life expectancy for a newly diagnosed young adult to 20–50 years. This is between two thirds and nearly that of the general population. If treatment is started late in the infection, prognosis is not as good: for example, if treatment is begun following the diagnosis of AIDS, life expectancy is ~10–40 years. Half of infants born with HIV die before two years of age without treatment.[clarification needed]
The primary causes of death from HIV/AIDS are opportunistic infections and cancer, both of which are frequently the result of the progressive failure of the immune system. Risk of cancer appears to increase once the CD4 count is below 500/μL. The rate of clinical disease progression varies widely between individuals and has been shown to be affected by a number of factors such as a person's susceptibility and immune function; their access to health care, the presence of co-infections; and the particular strain (or strains) of the virus involved.
Tuberculosis co-infection is one of the leading causes of sickness and death in those with HIV/AIDS being present in a third of all HIV-infected people and causing 25% of HIV-related deaths. HIV is also one of the most important risk factors for tuberculosis. Hepatitis C is another very common co-infection where each disease increases the progression of the other. The two most common cancers associated with HIV/AIDS are Kaposi's sarcoma and AIDS-related non-Hodgkin's lymphoma. Other cancers that are more frequent include anal cancer, Burkitt's lymphoma, primary central nervous system lymphoma, and cervical cancer.
Even with anti-retroviral treatment, over the long term HIV-infected people may experience neurocognitive disorders, osteoporosis, neuropathy, cancers, nephropathy, and cardiovascular disease. Some conditions, such as lipodystrophy, may be caused both by HIV and its treatment.
Some authors consider HIV/AIDS a global pandemic. As of 2016[update], approximately 36.7 million people worldwide have HIV, the number of new infections that year being about 1.8 million. This is down from 3.1 million new infections in 2001. Slightly over half the infected population are women and 2.1 million are children. It resulted in about 1 million deaths in 2016, down from a peak of 1.9 million in 2005.
Sub-Saharan Africa is the region most affected. In 2010, an estimated 68% (22.9 million) of all HIV cases and 66% of all deaths (1.2 million) occurred in this region. This means that about 5% of the adult population is infected and it is believed to be the cause of 10% of all deaths in children. Here, in contrast to other regions, women comprise nearly 60% of cases. South Africa has the largest population of people with HIV of any country in the world at 5.9 million. Life expectancy has fallen in the worst-affected countries due to HIV/AIDS; for example, in 2006 it was estimated that it had dropped from 65 to 35 years in Botswana. Mother-to-child transmission in Botswana and South Africa, as of 2013[update], has decreased to less than 5%, with improvement in many other African nations due to improved access to antiretroviral therapy.
South & South East Asia is the second most affected; in 2010 this region contained an estimated 4 million cases or 12% of all people living with HIV resulting in approximately 250,000 deaths. Approximately 2.4 million of these cases are in India.
During 2008 in the United States approximately 1.2 million people aged ≥13 years were living with HIV, resulting in about 17,500 deaths. The US Centers for Disease Control and Prevention estimated that in that year, 236,400 people or 20% of infected Americans were unaware of their infection. As of 2016[update] about 675,000 people have died of HIV/AIDS in the US since the beginning of the HIV epidemic. In the United Kingdom as of 2015[update], there were approximately 101,200 cases which resulted in 594 deaths. In Canada as of 2008, there were about 65,000 cases causing 53 deaths. Between the first recognition of AIDS (in 1981) and 2009, it has led to nearly 30 million deaths. Rates of HIV are lowest in North Africa and the Middle East (0.1% or less), East Asia (0.1%), and Western and Central Europe (0.2%). The worst-affected European countries, in 2009 and 2012 estimates, are Russia, Ukraine, Latvia, Moldova, Portugal and Belarus, in decreasing order of prevalence.
The first news story on the disease appeared on May 18, 1981, in the gay newspaper New York Native. AIDS was first clinically reported on June 5, 1981, with five cases in the United States. The initial cases were a cluster of injecting drug users and gay men with no known cause of impaired immunity who showed symptoms of Pneumocystis carinii pneumonia (PCP), a rare opportunistic infection that was known to occur in people with very compromised immune systems. Soon thereafter, a large number of homosexual men developed a generally rare skin cancer called Kaposi's sarcoma (KS). Many more cases of PCP and KS emerged, alerting U.S. Centers for Disease Control and Prevention (CDC) and a CDC task force was formed to monitor the outbreak.
In the early days, the CDC did not have an official name for the disease, often referring to it by way of diseases associated with it, such as lymphadenopathy, the disease after which the discoverers of HIV originally named the virus. They also used Kaposi's sarcoma and opportunistic infections, the name by which a task force had been set up in 1981. At one point the CDC referred to it as the "4H disease", as the syndrome seemed to affect heroin users, homosexuals, hemophiliacs, and Haitians. The term GRID, which stood for gay-related immune deficiency, had also been coined. However, after determining that AIDS was not isolated to the gay community, it was realized that the term GRID was misleading, and the term AIDS was introduced at a meeting in July 1982. By September 1982 the CDC started referring to the disease as AIDS.
In 1983, two separate research groups led by Robert Gallo and Luc Montagnier declared that a novel retrovirus may have been infecting people with AIDS, and published their findings in the same issue of the journal Science. Gallo claimed a virus which his group had isolated from a person with AIDS was strikingly similar in shape to other human T-lymphotropic viruses (HTLVs) that his group had been the first to isolate. Gallo's group called their newly isolated virus HTLV-III. At the same time, Montagnier's group isolated a virus from a person presenting with swelling of the lymph nodes of the neck and physical weakness, two characteristic symptoms of AIDS. Contradicting the report from Gallo's group, Montagnier and his colleagues showed that core proteins of this virus were immunologically different from those of HTLV-I. Montagnier's group named their isolated virus lymphadenopathy-associated virus (LAV). As these two viruses turned out to be the same, in 1986, LAV and HTLV-III were renamed HIV.
The origin of HIV / AIDS and the circumstances that led to its emergence remain unsolved.
Both HIV-1 and HIV-2 are believed to have originated in non-human primates in West-central Africa and were transferred to humans in the early 20th century. HIV-1 appears to have originated in southern Cameroon through the evolution of SIV(cpz), a simian immunodeficiency virus (SIV) that infects wild chimpanzees (HIV-1 descends from the SIVcpz endemic in the chimpanzee subspecies Pan troglodytes troglodytes). The closest relative of HIV-2 is SIV (smm), a virus of the sooty mangabey (Cercocebus atys atys), an Old World monkey living in coastal West Africa (from southern Senegal to western Ivory Coast). New World monkeys such as the owl monkey are resistant to HIV-1 infection, possibly because of a genomic fusion of two viral resistance genes. HIV-1 is thought to have jumped the species barrier on at least three separate occasions, giving rise to the three groups of the virus, M, N, and O.
There is evidence that humans who participate in bushmeat activities, either as hunters or as bushmeat vendors, commonly acquire SIV. However, SIV is a weak virus which is typically suppressed by the human immune system within weeks of infection. It is thought that several transmissions of the virus from individual to individual in quick succession are necessary to allow it enough time to mutate into HIV. Furthermore, due to its relatively low person-to-person transmission rate, SIV can only spread throughout the population in the presence of one or more high-risk transmission channels, which are thought to have been absent in Africa before the 20th century.
Specific proposed high-risk transmission channels, allowing the virus to adapt to humans and spread throughout society, depend on the proposed timing of the animal-to-human crossing. Genetic studies of the virus suggest that the most recent common ancestor of the HIV-1 M group dates back to c. 1910. Proponents of this dating link the HIV epidemic with the emergence of colonialism and growth of large colonial African cities, leading to social changes, including a higher degree of sexual promiscuity, the spread of prostitution, and the accompanying high frequency of genital ulcer diseases (such as syphilis) in nascent colonial cities. While transmission rates of HIV during vaginal intercourse are low under regular circumstances, they are increased manyfold if one of the partners has a sexually transmitted infection causing genital ulcers. Early 1900s colonial cities were notable for their high prevalence of prostitution and genital ulcers, to the degree that, as of 1928, as many as 45% of female residents of eastern Kinshasa were thought to have been prostitutes, and, as of 1933, around 15% of all residents of the same city had syphilis.
An alternative view holds that unsafe medical practices in Africa after World War II, such as unsterile reuse of single-use syringes during mass vaccination, antibiotic and anti-malaria treatment campaigns, were the initial vector that allowed the virus to adapt to humans and spread.
The earliest well-documented case of HIV in a human dates back to 1959 in the Congo. The virus may have been present in the U.S. as early as the mid-to-late 1950s, as a sixteen-year-old male named Robert Rayford presented with symptoms in 1966 and died in 1969. In the 1970s, there were cases of getting parasites and becoming sick with what was called "gay bowel disease", but what is now suspected to have been AIDS.
The earliest retrospectively described case of AIDS is believed to have been in Norway beginning in 1966, that of Arvid Noe. In July 1960, in the wake of Congo's independence, the United Nations recruited Francophone experts and technicians from all over the world to assist in filling administrative gaps left by Belgium, who did not leave behind an African elite to run the country. By 1962, Haitians made up the second-largest group of well-educated experts (out of the 48 national groups recruited), that totaled around 4500 in the country. Dr. Jacques Pépin, a Canadian author of The Origins of AIDS, stipulates that Haiti was one of HIV's entry points to the U.S. and that a Haitian may have carried HIV back across the Atlantic in the 1960s. Although there was known to have been at least one case of AIDS in the U.S. from 1966, the vast majority of infections occurring outside sub-Saharan Africa (including the U.S.) can be traced back to a single unknown individual who became infected with HIV in Haiti and brought the infection to the U.S. at some time around 1969. The epidemic rapidly spread among high-risk groups (initially, sexually promiscuous men who have sex with men). By 1978, the prevalence of HIV-1 among gay male residents of New York City and San Francisco was estimated at 5%, suggesting that several thousand individuals in the country had been infected.
Society and culture
AIDS stigma exists around the world in a variety of ways, including ostracism, rejection, discrimination and avoidance of HIV-infected people; compulsory HIV testing without prior consent or protection of confidentiality; violence against HIV-infected individuals or people who are perceived to be infected with HIV; and the quarantine of HIV-infected individuals. Stigma-related violence or the fear of violence prevents many people from seeking HIV testing, returning for their results, or securing treatment, possibly turning what could be a manageable chronic illness into a death sentence and perpetuating the spread of HIV.
AIDS stigma has been further divided into the following three categories:
- Instrumental AIDS stigma—a reflection of the fear and apprehension that are likely to be associated with any deadly and transmissible illness.
- Symbolic AIDS stigma—the use of HIV/AIDS to express attitudes toward the social groups or lifestyles perceived to be associated with the disease.
- Courtesy AIDS stigma—stigmatization of people connected to the issue of HIV/AIDS or HIV-positive people.
Often, AIDS stigma is expressed in conjunction with one or more other stigmas, particularly those associated with homosexuality, bisexuality, promiscuity, prostitution, and intravenous drug use.
In many developed countries, there is an association between AIDS and homosexuality or bisexuality, and this association is correlated with higher levels of sexual prejudice, such as anti-homosexual or anti-bisexual attitudes. There is also a perceived association between AIDS and all male-male sexual behavior, including sex between uninfected men. However, the dominant mode of spread worldwide for HIV remains heterosexual transmission. To get a better understanding of the anti-homosexual attitudes around AIDs the musical Rent explores this.
In 2003, as part of an overall reform of marriage and population legislation, it became legal for those diagnosed with AIDS to marry in China.
In 2013, the U.S. National Library of Medicine developed a traveling exhibition titled Surviving and Thriving: AIDS, Politics, and Culture; this covered medical research, the U.S. government's response, and personal stories from people with AIDS, caregivers, and activists.
HIV/AIDS affects the economics of both individuals and countries. The gross domestic product of the most affected countries has decreased due to the lack of human capital. Without proper nutrition, health care and medicine, large numbers of people die from AIDS-related complications. Before death they will not only be unable to work, but will also require significant medical care. It is estimated that as of 2007 there were 12 million AIDS orphans. Many are cared for by elderly grandparents.
Returning to work after beginning treatment for HIV/AIDS is difficult, and affected people often work less than the average worker. Unemployment in people with HIV/AIDS also is associated with suicidal ideation, memory problems, and social isolation. Employment increases self-esteem, sense of dignity, confidence, and quality of life for people with HIV/AIDS. Anti-retroviral treatment may help people with HIV/AIDS work more, and may increase the chance that a person with HIV/AIDS will be employed (low-quality evidence).
By affecting mainly young adults, AIDS reduces the taxable population, in turn reducing the resources available for public expenditures such as education and health services not related to AIDS, resulting in increasing pressure on the state's finances and slower growth of the economy. This causes a slower growth of the tax base, an effect that is reinforced if there are growing expenditures on treating the sick, training (to replace sick workers), sick pay, and caring for AIDS orphans. This is especially true if the sharp increase in adult mortality shifts the responsibility from the family to the government in caring for these orphans.
At the household level, AIDS causes both loss of income and increased spending on healthcare. A study in Côte d'Ivoire showed that households having a person with HIV/AIDS spent twice as much on medical expenses as other households. This additional expenditure also leaves less income to spend on education and other personal or family investment.
Religion and AIDS
The topic of religion and AIDS has become highly controversial, primarily because some religious authorities have publicly declared their opposition to the use of condoms. The religious approach to prevent the spread of AIDS, according to a report by American health expert Matthew Hanley titled The Catholic Church and the Global AIDS Crisis, argues that cultural changes are needed, including a re-emphasis on fidelity within marriage and sexual abstinence outside of it.
Some religious organizations have claimed that prayer can cure HIV/AIDS. In 2011, the BBC reported that some churches in London were claiming that prayer would cure AIDS, and the Hackney-based Centre for the Study of Sexual Health and HIV reported that several people stopped taking their medication, sometimes on the direct advice of their pastor, leading to many deaths. The Synagogue Church Of All Nations advertised an "anointing water" to promote God's healing, although the group denies advising people to stop taking medication.
One of the first high-profile cases of AIDS was the American gay actor Rock Hudson. He had been diagnosed during 1984, announced that he had had the virus on July 25, 1985, and died a few months later on October 2, 1985. Another notable British casualty of AIDS that year was Nicholas Eden, a gay politician and son of former prime minister Anthony Eden. On November 24, 1991, the virus claimed the life of British rock star Freddie Mercury, lead singer of the band Queen, who died from an AIDS-related illness having only revealed the diagnosis on the previous day.
One of the first high-profile heterosexual cases of the virus was American tennis player Arthur Ashe. He was diagnosed as HIV-positive on August 31, 1988, having contracted the virus from blood transfusions during heart surgery earlier in the 1980s. Further tests within 24 hours of the initial diagnosis revealed that Ashe had AIDS, but he did not tell the public about his diagnosis until April 1992. He died as a result on February 6, 1993, aged 49.
Therese Frare's photograph of gay activist David Kirby, as he lay dying from AIDS while surrounded by family, was taken in April 1990. Life magazine said the photo became the one image "most powerfully identified with the HIV/AIDS epidemic." The photo was displayed in Life, was the winner of the World Press Photo, and acquired worldwide notoriety after being used in a United Colors of Benetton advertising campaign in 1992.
Many famous artists and AIDS activists such as Larry Kramer, Diamanda Galás and Rosa von Praunheim campaign for AIDS education and the rights of those affected. These artists worked with various media formats.
Criminal transmission of HIV is the intentional or reckless infection of a person with the human immunodeficiency virus (HIV). Some countries or jurisdictions, including some areas of the United States, have laws that criminalize HIV transmission or exposure. Others may charge the accused under laws enacted before the HIV pandemic.
In 1996, Ugandan-born Canadian Johnson Aziga was diagnosed with HIV; he subsequently had unprotected sex with eleven women without disclosing his diagnosis. By 2003, seven had contracted HIV; two died from complications related to AIDS. Aziga was convicted of first-degree murder and sentenced to life imprisonment.
There are many misconceptions about HIV and AIDS. Three misconceptions are that AIDS can spread through casual contact, that sexual intercourse with a virgin will cure AIDS, and that HIV can infect only gay men and drug users. In 2014, some among the British public wrongly thought one could get HIV from kissing (16%), sharing a glass (5%), spitting (16%), a public toilet seat (4%), and coughing or sneezing (5%). Other misconceptions are that any act of anal intercourse between two uninfected gay men can lead to HIV infection, and that open discussion of HIV and homosexuality in schools will lead to increased rates of AIDS.
A small group of individuals continue to dispute the connection between HIV and AIDS, the existence of HIV itself, or the validity of HIV testing and treatment methods. These claims, known as AIDS denialism, have been examined and rejected by the scientific community. However, they have had a significant political impact, particularly in South Africa, where the government's official embrace of AIDS denialism (1999–2005) was responsible for its ineffective response to that country's AIDS epidemic, and has been blamed for hundreds of thousands of avoidable deaths and HIV infections.
Several discredited conspiracy theories have held that HIV was created by scientists, either inadvertently or deliberately. Operation INFEKTION was a worldwide Soviet active measures operation to spread the claim that the United States had created HIV/AIDS. Surveys show that a significant number of people believed—and continue to believe—in such claims.
At the peak of the HIV/AIDS outbreak, there was also misinformation spread from some governmental institutions. For example, Anthony Fauci, head of the National Institute of Allergy and Infectious Diseases during the AIDS outbreak, stated in the context of a conversation about childhood infections, “if the close contact of a child is a household contact, perhaps there will be a certain number of cases of individuals who are just living with and in close contact with someone with AIDS, or at risk of AIDS, who does not necessarily have to have intimate sexual contact or share a needle, but just the ordinary close contact that one sees in normal interpersonal relations.” This and similar statements made by governmental agencies potentially fueled the unfounded fear that the public had that AIDS could be spread by ordinary close contact rather than through sexual or fluid transmission as is most commonly the case.
HIV/AIDS research includes all medical research which attempts to prevent, treat, or cure HIV/AIDS, along with fundamental research about the nature of HIV as an infectious agent, and about AIDS as the disease caused by HIV.
Many governments and research institutions participate in HIV/AIDS research. This research includes behavioral health interventions such as sex education, and drug development, such as research into microbicides for sexually transmitted diseases, HIV vaccines, and antiretroviral drugs. Other medical research areas include the topics of pre-exposure prophylaxis, post-exposure prophylaxis, and circumcision and HIV. Public health officials, researchers, and programs can gain a more comprehensive picture of the barriers they face, and the efficacy of current approaches to HIV treatment and prevention, by tracking standard HIV indicators. Use of common indicators is an increasing focus of development organizations and researchers.
- ^ a b c d "What Are HIV and AIDS? | HIV.gov". www.hiv.gov. U.S. Department of Health and Human Services (HHS). May 15, 2017. Archived from the original on September 22, 2019. Retrieved September 10, 2017.
- ^ "HIV Classification: CDC and WHO Staging Systems | AIDS Education and Training Centers National Coordinating Resource Center (AETC NCRC)". aidsetc.org. AIDS Education and Training Center Program. Archived from the original on October 18, 2017. Retrieved September 10, 2017.
- ^ "Wear your red ribbon this World AIDS Day | UNAIDS". www.unaids.org. UNAIDS Secretariat. Archived from the original on September 10, 2017. Retrieved September 10, 2017.
- ^ a b c d e f g h i j k l m "HIV/AIDS Fact sheet N°360". World Health Organization. November 2015. Archived from the original on February 17, 2016. Retrieved February 11, 2016.
- ^ a b c d e "About HIV/AIDS". CDC. December 6, 2015. Archived from the original on February 24, 2016. Retrieved February 11, 2016.
- ^ a b c UNAIDS (May 18, 2012). "The quest for an HIV vaccine". Archived from the original on May 24, 2012.
- ^ a b c UNAIDS, World Health Organization (December 2007). "2007 AIDS epidemic update" (PDF). Archived from the original (PDF) on May 27, 2008. Retrieved March 12, 2008.
- ^ a b c d e f "Global HIV & AIDS statistics — 2021 fact sheet". www.unaids.org. UNAIDS. Retrieved July 17, 2021.
- ^ Sepkowitz KA (June 2001). "AIDS – the first 20 years". The New England Journal of Medicine. 344 (23): 1764–72. doi:10.1056/NEJM200106073442306. PMID 11396444.
- ^ Krämer A, Kretzschmar M, Krickeberg K (2010). Modern infectious disease epidemiology concepts, methods, mathematical models, and public health (Online-Ausg. ed.). New York: Springer. p. 88. ISBN 978-0-387-93835-6. Archived from the original on September 24, 2015. Retrieved June 27, 2015.
- ^ Kirch W (2008). Encyclopedia of Public Health. New York: Springer. pp. 676–77. ISBN 978-1-4020-5613-0. Archived from the original on September 11, 2015. Retrieved June 27, 2015.
- ^ "Retrovirus Definition". AIDSinfo. Archived from the original on December 28, 2019. Retrieved December 28, 2019.
- ^ a b c d e f g h i Rom WN, Markowitz SB, eds. (2007). Environmental and occupational medicine (4th ed.). Philadelphia: Wolters Kluwer/Lippincott Williams & Wilkins. p. 745. ISBN 978-0-7817-6299-1. Archived from the original on September 11, 2015. Retrieved June 27, 2015.
- ^ "HIV and Its Transmission". Centers for Disease Control and Prevention. 2003. Archived from the original on February 4, 2005. Retrieved May 23, 2006.
- ^ "Preventing Sexual Transmission of HIV". HIV.gov. April 9, 2021. Retrieved February 1, 2022.
- ^ a b Gallo RC (October 2006). "A reflection on HIV/AIDS research after 25 years". Retrovirology. 3 (1): 72. doi:10.1186/1742-4690-3-72. PMC 1629027. PMID 17054781.
- ^ a b c "The impact of AIDS on people and societies" (PDF). 2006 Report on the global AIDS epidemic. UNAIDS. 2006. ISBN 978-92-9173-479-5.
- ^ Endersby, Jim (2016). "Myth Busters". Science. 351 (6268): 35. Bibcode:2016Sci...351...35E. doi:10.1126/science.aad2891. S2CID 51608938. Archived from the original on February 22, 2016. Retrieved February 14, 2016.
- ^ McCullom, Rob (February 26, 2013). "An African Pope Won't Change the Vatican's Views on Condoms and AIDS". The Atlantic. Archived from the original on March 8, 2016. Retrieved February 14, 2016.
- ^ Harden, Victoria Angela (2012). AIDS at 30: A History. Potomac Books Inc. p. 324. ISBN 978-1-59797-294-9.
- ^ a b Sharp PM, Hahn BH (September 2011). "Origins of HIV and the AIDS pandemic". Cold Spring Harbor Perspectives in Medicine. 1 (1): a006841. doi:10.1101/cshperspect.a006841. PMC 3234451. PMID 22229120.
- ^ "HIV Statistics Overview (International Statistics)". Centers for Disease Control and Prevention. 2018. Retrieved May 9, 2021.
- ^ "Fact Sheet – World AIDS Day 2019" (PDF). www.unaids.org. Archived (PDF) from the original on December 21, 2019. Retrieved December 21, 2019.
- ^ a b Kallings LO (March 2008). "The first postmodern pandemic: 25 years of HIV/AIDS". Journal of Internal Medicine. 263 (3): 218–43. doi:10.1111/j.1365-2796.2007.01910.x. PMID 18205765. S2CID 205339589.(subscription required)
- ^ "NIH launches new collaboration to develop gene-based cures for sickle cell disease and HIV on global scale". National Institutes of Health (NIH). October 23, 2019. Retrieved September 24, 2021.
- ^ a b Guideline on when to start antiretroviral therapy and on pre-exposure prophylaxis for HIV (PDF). World Health Organization. 2015. p. 13. ISBN 978-92-4-150956-5. Archived (PDF) from the original on October 14, 2015.
- ^ a b c d e f Mandell, Bennett, and Dolan (2010). Chapter 121.
- ^ a b c d e f g h i j k l m n o p WHO case definitions of HIV for surveillance and revised clinical staging and immunological classification of HIV-related disease in adults and children (PDF). Geneva: World Health Organization. 2007. pp. 6–16. ISBN 978-92-4-159562-9. Archived (PDF) from the original on October 31, 2013.
- ^ Diseases and disorders. Tarrytown, NY: Marshall Cavendish. 2008. p. 25. ISBN 978-0-7614-7771-6. Archived from the original on September 19, 2015. Retrieved June 27, 2015.
- ^ a b c d e f g h i j k l m n o Mandell, Bennett, and Dolan (2010). Chapter 118.
- ^ a b c d e f g h i j k l m n o p q r Vogel M, Schwarze-Zander C, Wasmuth JC, Spengler U, Sauerbruch T, Rockstroh JK (July 2010). "The treatment of patients with HIV". Deutsches Ärzteblatt International. 107 (28–29): 507–15, quiz 516. doi:10.3238/arztebl.2010.0507. PMC 2915483. PMID 20703338.
- ^ Evian, Clive (2006). Primary HIV/AIDS care: a practical guide for primary health care personnel in a clinical and supportive setting (Updated 4th ed.). Houghton [South Africa]: Jacana. p. 29. ISBN 978-1-77009-198-6. Archived from the original on September 11, 2015. Retrieved June 27, 2015.
- ^ Charles B. Hicks, MD (2001). Jacques W.A.J. Reeders & Philip Charles Goodman (ed.). Radiology of AIDS. Berlin [u.a.]: Springer. p. 19. ISBN 978-3-540-66510-6. Archived from the original on May 9, 2016. Retrieved June 27, 2015.
- ^ Elliott, Tom (2012). Lecture Notes: Medical Microbiology and Infection. John Wiley & Sons. p. 273. ISBN 978-1-118-37226-5. Archived from the original on September 19, 2015. Retrieved June 27, 2015.
- ^ a b Blankson JN (March 2010). "Control of HIV-1 replication in elite suppressors". Discovery Medicine. 9 (46): 261–66. PMID 20350494.
- ^ Walker BD (August–September 2007). "Elite control of HIV Infection: implications for vaccines and treatment". Topics in HIV Medicine. 15 (4): 134–36. PMID 17720999.
- ^ Holmes CB, Losina E, Walensky RP, Yazdanpanah Y, Freedberg KA (March 2003). "Review of human immunodeficiency virus type 1-related opportunistic infections in sub-Saharan Africa". Clinical Infectious Diseases. 36 (5): 652–62. doi:10.1086/367655. PMID 12594648.
- ^ Chu C, Selwyn PA (February 2011). "Complications of HIV infection: a systems-based approach". American Family Physician. 83 (4): 395–406. PMID 21322514.
- ^ a b c d e Mandell, Bennett, and Dolan (2010). Chapter 169.
- ^ Mittal R, Rath S, Vemuganti GK (July 2013). "Ocular surface squamous neoplasia – Review of etio-pathogenesis and an update on clinico-pathological diagnosis". Saudi Journal of Ophthalmology. 27 (3): 177–86. doi:10.1016/j.sjopt.2013.07.002. PMC 3770226. PMID 24227983.
- ^ "AIDS". MedlinePlus. A.D.A.M. Archived from the original on June 18, 2012. Retrieved June 14, 2012.
- ^ Sestak K (July 2005). "Chronic diarrhea and AIDS: insights into studies with non-human primates". Current HIV Research. 3 (3): 199–205. doi:10.2174/1570162054368084. PMID 16022653.
- ^ Murray ED, Buttner N, Price BH (2012). "Depression and Psychosis in Neurological Practice". In Bradley WG, Daroff RB, Fenichel GM, Jankovic J (eds.). Bradley's Neurology in Clinical Practice: Expert Consult – Online and Print, 6e (Bradley, Neurology in Clinical Practice e-dition 2v Set). Vol. 1 (6th ed.). Philadelphia: Elsevier/Saunders. p. 101. ISBN 978-1-4377-0434-1.
- ^ a b Donegan, Elizabeth; Stuart, Maria; Niland, Joyce C.; Sacks, Henry S.; Azen, Stanley P.; Dietrich, Shelby L.; Faucett, Cheryl; Fletcher, Mary Ann; Kleinman, Steven H.; Operskalski, Eva A.; Perkins, Herbert A.; Pindyck, Johanna; Schiff, Eugene R.; Stites, Daniel P.; Tomasulo, Peter A.; Mosley, James W. (November 15, 1990). "Infection with Human Immunodeficiency Virus Type 1 (HIV-1) among Recipients of Antibody-Positive Blood Donations". Annals of Internal Medicine. 113 (10): 733–739. doi:10.7326/0003-4819-113-10-733. Retrieved May 11, 2020.
- ^ Coovadia H (2004). "Antiretroviral agents—how best to protect infants from HIV and save their mothers from AIDS". N. Engl. J. Med. 351 (3): 289–292. doi:10.1056/NEJMe048128. PMID 15247337.
- ^ Smith DK, Grohskopf LA, Black RJ, Auerbach JD, Veronese F, Struble KA, Cheever L, Johnson M, Paxton LA, Onorato IM, Greenberg AE (January 21, 2005). "Antiretroviral postexposure prophylaxis after sexual, injection-drug use, or other nonoccupational exposure to HIV in the United States: recommendations from the U.S. Department of Health and Human Services". MMWR. Recommendations and reports : Morbidity and mortality weekly report. Recommendations and reports / Centers for Disease Control. 54 (RR-2): 1–20. PMID 15660015.
- ^ Kripke C (August 1, 2007). "Antiretroviral prophylaxis for occupational exposure to HIV". American Family Physician. 76 (3): 375–6. PMID 17708137.
- ^ a b c d Dosekun O, Fox J (July 2010). "An overview of the relative risks of different sexual behaviours on HIV transmission". Current Opinion in HIV and AIDS. 5 (4): 291–7. doi:10.1097/COH.0b013e32833a88a3. PMID 20543603.
- ^ Cunha, Burke (2012). Antibiotic Essentials 2012 (11 ed.). Jones & Bartlett Publishers. p. 303. ISBN 9781449693831.
- ^ a b Boily MC, Baggaley RF, Wang L, Masse B, White RG, Hayes RJ, Alary M (February 2009). "Heterosexual risk of HIV-1 infection per sexual act: systematic review and meta-analysis of observational studies". The Lancet Infectious Diseases. 9 (2): 118–29. doi:10.1016/S1473-3099(09)70021-0. PMC 4467783. PMID 19179227.
- ^ Baggaley RF, White RG, Boily MC (December 2008). "Systematic review of orogenital HIV-1 transmission probabilities". International Journal of Epidemiology. 37 (6): 1255–65. doi:10.1093/ije/dyn151. PMC 2638872. PMID 18664564.
- ^ a b c Kripke C (August 2007). "Antiretroviral prophylaxis for occupational exposure to HIV". American Family Physician. 76 (3): 375–76. PMID 17708137.
- ^ van der Kuyl AC, Cornelissen M (September 2007). "Identifying HIV-1 dual infections". Retrovirology. 4: 67. doi:10.1186/1742-4690-4-67. PMC 2045676. PMID 17892568.
- ^ McCray, Eugene; Mermin, Jonathan (September 27, 2017). "Dear Colleague: September 27, 2017". Division of HIV/AIDS Prevention. Centers for Disease Control and Prevention. Archived from the original on January 30, 2018. Retrieved February 1, 2018.
- ^ LeMessurier, J; Traversy, G; Varsaneux, O; Weekes, M; Avey, MT; Niragira, O; Gervais, R; Guyatt, G; Rodin, R (November 19, 2018). "Risk of sexual transmission of human immunodeficiency virus with antiretroviral therapy, suppressed viral load and condom use: a systematic review". Canadian Medical Association Journal. 190 (46): E1350–E1360. doi:10.1503/cmaj.180311. PMC 6239917. PMID 30455270.
- ^ Vernazza, P; Bernard, EJ (January 29, 2016). "HIV is not transmitted under fully suppressive therapy: The Swiss Statement – eight years later". Swiss Medical Weekly. 146: w14246. doi:10.4414/smw.2016.14246. PMID 26824882.
- ^ "HIV and Men". Centers for Disease Control and Prevention. U.S. Department of Health & Human Services. Archived from the original on December 1, 2019. Retrieved November 3, 2019.
- ^ "HIV and Gay and Bisexual Men". Centers for Disease Control and Prevention. U.S. Department of Health & Human Services. Archived from the original on November 2, 2019. Retrieved November 3, 2019.
- ^ "HIV Among Gay and Bisexual Men" (PDF). Archived (PDF) from the original on December 18, 2016. Retrieved January 1, 2017.
- ^ a b c d e f g Boily MC, Baggaley RF, Wang L, Masse B, White RG, Hayes RJ, Alary M (February 2009). "Heterosexual risk of HIV-1 infection per sexual act: systematic review and meta-analysis of observational studies". The Lancet. Infectious Diseases. 9 (2): 118–29. doi:10.1016/S1473-3099(09)70021-0. PMC 4467783. PMID 19179227.
- ^ Beyrer C, Baral SD, van Griensven F, Goodreau SM, Chariyalertsak S, Wirtz AL, Brookmeyer R (July 2012). "Global epidemiology of HIV infection in men who have sex with men". The Lancet. 380 (9839): 367–77. doi:10.1016/S0140-6736(12)60821-6. PMC 3805037. PMID 22819660.
- ^ Yu M, Vajdy M (August 2010). "Mucosal HIV transmission and vaccination strategies through oral compared with vaginal and rectal routes". Expert Opinion on Biological Therapy. 10 (8): 1181–95. doi:10.1517/14712598.2010.496776. PMC 2904634. PMID 20624114.
- ^ Stürchler, Dieter A. (2006). Exposure a guide to sources of infections. Washington, DC: ASM Press. p. 544. ISBN 978-1-55581-376-5. Archived from the original on November 30, 2015. Retrieved June 27, 2015.
- ^ Pattman R, et al., eds. (2010). Oxford handbook of genitourinary medicine, HIV, and sexual health (2nd ed.). Oxford: Oxford University Press. p. 95. ISBN 978-0-19-957166-6.
- ^ a b c Dosekun O, Fox J (July 2010). "An overview of the relative risks of different sexual behaviours on HIV transmission". Current Opinion in HIV and AIDS. 5 (4): 291–97. doi:10.1097/COH.0b013e32833a88a3. PMID 20543603. S2CID 25541753.
- ^ a b Ng BE, Butler LM, Horvath T, Rutherford GW (March 2011). Butler LM (ed.). "Population-based biomedical sexually transmitted infection control interventions for reducing HIV infection". The Cochrane Database of Systematic Reviews (3): CD001220. doi:10.1002/14651858.CD001220.pub3. PMID 21412869.
- ^ Anderson J (February 2012). "Women and HIV: motherhood and more". Current Opinion in Infectious Diseases. 25 (1): 58–65. doi:10.1097/QCO.0b013e32834ef514. PMID 22156896. S2CID 6198083.
- ^ Kerrigan, Deanna (2012). The Global HIV Epidemics among Sex Workers. World Bank Publications. pp. 1–5. ISBN 978-0-8213-9775-6. Archived from the original on September 19, 2015. Retrieved June 27, 2015.
- ^ Aral, Sevgi (2013). The New Public Health and STD/HIV Prevention: Personal, Public and Health Systems Approaches. Springer. p. 120. ISBN 978-1-4614-4526-5. Archived from the original on September 24, 2015. Retrieved June 27, 2015.
- ^ Klimas N, Koneru AO, Fletcher MA (June 2008). "Overview of HIV". Psychosomatic Medicine. 70 (5): 523–30. doi:10.1097/PSY.0b013e31817ae69f. PMID 18541903. S2CID 38476611.
- ^ Draughon JE, Sheridan DJ (2012). "Nonoccupational postexposure prophylaxis following sexual assault in industrialized low-HIV-prevalence countries: a review". Psychology, Health & Medicine. 17 (2): 235–54. doi:10.1080/13548506.2011.579984. PMID 22372741. S2CID 205771853.
- ^ Baggaley RF, Boily MC, White RG, Alary M (April 2006). "Risk of HIV-1 transmission for parenteral exposure and blood transfusion: a systematic review and meta-analysis". AIDS. 20 (6): 805–12. doi:10.1097/01.aids.0000218543.46963.6d. PMID 16549963. S2CID 22674060.
- ^ "Needlestick Prevention Guide" (PDF). 2002. pp. 5–6. Archived (PDF) from the original on July 12, 2018. Retrieved November 10, 2019.
- ^ "HIV in the United States: An Overview". Center for Disease Control and Prevention. March 2012. Archived from the original on May 1, 2013.
- ^ "Will I need a blood transfusion?" (PDF). NHS patient information. National Health Services. 2011. Archived (PDF) from the original on October 25, 2012. Retrieved August 29, 2012.
- ^ Centers for Disease Control Prevention (CDC) (October 2010). "HIV transmission through transfusion – Missouri and Colorado, 2008". Morbidity and Mortality Weekly Report. 59 (41): 1335–39. PMID 20966896.
- ^ UNAIDS 2011 pg. 60–70
- ^ "Blood safety ... for too few". World Health Organization. 2001. Archived from the original on January 17, 2005.
- ^ Simonds RJ (November 1993). "HIV transmission by organ and tissue transplantation". AIDS. 7 Suppl 2: S35–38. doi:10.1097/00002030-199311002-00008. PMID 8161444. S2CID 28488664.
- ^ a b c Reid SR (August 2009). "Injection drug use, unsafe medical injections, and HIV in Africa: a systematic review". Harm Reduction Journal. 6: 24. doi:10.1186/1477-7517-6-24. PMC 2741434. PMID 19715601.
- ^ a b "Basic Information about HIV and AIDS". Center for Disease Control and Prevention. April 2012. Archived from the original on June 18, 2017.
- ^ Crans, Wayne J. (June 1, 2010). "Why Mosquitoes Cannot Transmit AIDS". rci.rutgers.edu. Rutgers University. New Jersey Agricultural Experiment Station Publication No. H-40101-01-93. Archived from the original on March 29, 2014. Retrieved March 29, 2014.
- ^ "Preventing Mother-to-Child Transmission of HIV". HIV.gov. Archived from the original on December 9, 2017. Retrieved December 8, 2017.
- ^ a b c d Coutsoudis A, Kwaan L, Thomson M (October 2010). "Prevention of vertical transmission of HIV-1 in resource-limited settings". Expert Review of Anti-Infective Therapy. 8 (10): 1163–75. doi:10.1586/eri.10.94. PMID 20954881. S2CID 46624541.
- ^ "WHO | Mother-to-child transmission of HIV". WHO. Archived from the original on October 18, 2019. Retrieved December 27, 2019.
- ^ White AB, Mirjahangir JF, Horvath H, Anglemyer A, Read JS (October 2014). "Antiretroviral interventions for preventing breast milk transmission of HIV". The Cochrane Database of Systematic Reviews. 10 (10): CD011323. doi:10.1002/14651858.CD011323. PMID 25280769.
- ^ a b c "Infant feeding in the context of HIV". www.who.int. April 2011. Archived from the original on March 9, 2017. Retrieved March 9, 2017.
- ^ Alimonti JB, Ball TB, Fowke KR (July 2003). "Mechanisms of CD4+ T lymphocyte cell death in human immunodeficiency virus infection and AIDS". The Journal of General Virology. 84 (Pt 7): 1649–61. doi:10.1099/vir.0.19110-0. PMID 12810858.
- ^ International Committee on Taxonomy of Viruses (2002). "61.0.6. Lentivirus". National Institutes of Health. Archived from the original on April 18, 2006. Retrieved June 25, 2012.
- ^ International Committee on Taxonomy of Viruses (2002). "61. Retroviridae". National Institutes of Health. Archived from the original on December 17, 2001. Retrieved June 25, 2012.
- ^ Levy JA (November 1993). "HIV pathogenesis and long-term survival". AIDS. 7 (11): 1401–10. doi:10.1097/00002030-199311000-00001. PMID 8280406.
- ^ Smith JA, Daniel R (May 2006). "Following the path of the virus: the exploitation of host DNA repair mechanisms by retroviruses". ACS Chemical Biology. 1 (4): 217–26. doi:10.1021/cb600131q. PMID 17163676.
- ^ Martínez MA, ed. (2010). RNA interference and viruses : current innovations and future trends. Norfolk: Caister Academic Press. p. 73. ISBN 978-1-904455-56-1. Archived from the original on September 11, 2015. Retrieved June 27, 2015.
- ^ Gerald B. Pier, ed. (2004). Immunology, infection, and immunity. Washington, DC: ASM Press. p. 550. ISBN 978-1-55581-246-1. Archived from the original on May 9, 2016. Retrieved June 27, 2015.
- ^ a b c Zhang C, Zhou S, Groppelli E, Pellegrino P, Williams I, Borrow P, Chain BM, Jolly C (April 2015). "Hybrid spreading mechanisms and T cell activation shape the dynamics of HIV-1 infection". PLOS Computational Biology. 11 (4): e1004179. arXiv:1503.08992. Bibcode:2015PLSCB..11E4179Z. doi:10.1371/journal.pcbi.1004179. PMC 4383537. PMID 25837979.
- ^ Jolly C, Kashefi K, Hollinshead M, Sattentau QJ (January 2004). "HIV-1 cell to cell transfer across an Env-induced, actin-dependent synapse". The Journal of Experimental Medicine. 199 (2): 283–93. doi:10.1084/jem.20030648. PMC 2211771. PMID 14734528.
- ^ Sattentau Q (November 2008). "Avoiding the void: cell-to-cell spread of human viruses". Nature Reviews. Microbiology. 6 (11): 815–26. doi:10.1038/nrmicro1972. PMID 18923409. S2CID 20991705.
- ^ Sigal A, Kim JT, Balazs AB, Dekel E, Mayo A, Milo R, Baltimore D (August 2011). "Cell-to-cell spread of HIV permits ongoing replication despite antiretroviral therapy" (PDF). Nature. 477 (7362): 95–98. Bibcode:2011Natur.477...95S. doi:10.1038/nature10347. PMID 21849975. S2CID 4409389.
- ^ Gilbert PB, McKeague IW, Eisen G, Mullins C, Guéye-NDiaye A, Mboup S, Kanki PJ (February 2003). "Comparison of HIV-1 and HIV-2 infectivity from a prospective cohort study in Senegal". Statistics in Medicine. 22 (4): 573–93. doi:10.1002/sim.1342. PMID 12590415. S2CID 28523977.
- ^ a b Reeves JD, Doms RW (June 2002). "Human immunodeficiency virus type 2". The Journal of General Virology. 83 (Pt 6): 1253–65. doi:10.1099/0022-1317-83-6-1253. PMID 12029140.
- ^ Piatak M, Saag MS, Yang LC, Clark SJ, Kappes JC, Luk KC, Hahn BH, Shaw GM, Lifson JD (March 1993). "High levels of HIV-1 in plasma during all stages of infection determined by competitive PCR". Science. 259 (5102): 1749–54. Bibcode:1993Sci...259.1749P. doi:10.1126/science.8096089. PMID 8096089. S2CID 12158927.
- ^ Pantaleo G, Demarest JF, Schacker T, Vaccarezza M, Cohen OJ, Daucher M, Graziosi C, Schnittman SS, Quinn TC, Shaw GM, Perrin L, Tambussi G, Lazzarin A, Sekaly RP, Soudeyns H, Corey L, Fauci AS (January 1997). "The qualitative nature of the primary immune response to HIV infection is a prognosticator of disease progression independent of the initial level of plasma viremia". Proceedings of the National Academy of Sciences of the United States of America. 94 (1): 254–58. Bibcode:1997PNAS...94..254P. doi:10.1073/pnas.94.1.254. PMC 19306. PMID 8990195.
- ^ Hel Z, McGhee JR, Mestecky J (June 2006). "HIV infection: first battle decides the war". Trends in Immunology. 27 (6): 274–81. doi:10.1016/j.it.2006.04.007. PMID 16679064.
- ^ Pillay, Deenan; Genetti, Anna Maria; Weiss, Robin A. (2007). "Human Immunodeficiency Viruses". In Zuckerman, Arie J.; et al. (eds.). Principles and practice of clinical virology (6th ed.). Hoboken, NJ: Wiley. p. 905. ISBN 978-0-470-51799-4.
- ^ Mehandru S, Poles MA, Tenner-Racz K, Horowitz A, Hurley A, Hogan C, Boden D, Racz P, Markowitz M (September 2004). "Primary HIV-1 infection is associated with preferential depletion of CD4+ T lymphocytes from effector sites in the gastrointestinal tract". The Journal of Experimental Medicine. 200 (6): 761–70. doi:10.1084/jem.20041196. PMC 2211967. PMID 15365095.
- ^ Brenchley JM, Schacker TW, Ruff LE, Price DA, Taylor JH, Beilman GJ, Nguyen PL, Khoruts A, Larson M, Haase AT, Douek DC (September 2004). "CD4+ T cell depletion during all stages of HIV disease occurs predominantly in the gastrointestinal tract". The Journal of Experimental Medicine. 200 (6): 749–59. doi:10.1084/jem.20040874. PMC 2211962. PMID 15365096.
- ^ Olson WC, Jacobson JM (March 2009). "CCR5 monoclonal antibodies for HIV-1 therapy". Current Opinion in HIV and AIDS. 4 (2): 104–11. doi:10.1097/COH.0b013e3283224015. PMC 2760828. PMID 19339948.
- ^ a b Aliberti, Julio, ed. (2011). Control of Innate and Adaptive Immune Responses During Infectious Diseases. New York: Springer Verlag. p. 145. ISBN 978-1-4614-0483-5. Archived from the original on September 24, 2015. Retrieved June 27, 2015.
- ^ Appay V, Sauce D (January 2008). "Immune activation and inflammation in HIV-1 infection: causes and consequences". The Journal of Pathology. 214 (2): 231–41. doi:10.1002/path.2276. PMID 18161758. S2CID 26830006.
- ^ Brenchley JM, Price DA, Schacker TW, Asher TE, Silvestri G, Rao S, Kazzaz Z, Bornstein E, Lambotte O, Altmann D, Blazar BR, Rodriguez B, Teixeira-Johnson L, Landay A, Martin JN, Hecht FM, Picker LJ, Lederman MM, Deeks SG, Douek DC (December 2006). "Microbial translocation is a cause of systemic immune activation in chronic HIV infection". Nature Medicine. 12 (12): 1365–71. doi:10.1038/nm1511. PMC 1717013. PMID 17115046.
- ^ "HIV/AIDS Testing". CDC. March 16, 2018. Archived from the original on April 14, 2018. Retrieved April 14, 2018.
- ^ a b US Preventive Services Task, Force.; Owens, DK; Davidson, KW; Krist, AH; Barry, MJ; Cabana, M; Caughey, AB; Curry, SJ; Doubeni, CA; Epling JW, Jr; Kubik, M; Landefeld, CS; Mangione, CM; Pbert, L; Silverstein, M; Simon, MA; Tseng, CW; Wong, JB (June 18, 2019). "Screening for HIV Infection: US Preventive Services Task Force Recommendation Statement". JAMA. 321 (23): 2326–2336. doi:10.1001/jama.2019.6587. PMID 31184701.
- ^ a b Kellerman S, Essajee S (July 2010). "HIV testing for children in resource-limited settings: what are we waiting for?". PLOS Medicine. 7 (7): e1000285. doi:10.1371/journal.pmed.1000285. PMC 2907270. PMID 20652012.
- ^ a b c UNAIDS 2011 pg. 70–80
- ^ a b c Schneider E, Whitmore S, Glynn KM, Dominguez K, Mitsch A, McKenna MT (December 2008). "Revised surveillance case definitions for HIV infection among adults, adolescents, and children aged <18 months and for HIV infection and AIDS among children aged 18 months to <13 years – United States, 2008" (PDF). MMWR. Recommendations and Reports. 57 (RR-10): 1–12. PMID 19052530.
- ^ a b c Centers for Disease Control Prevention (CDC) (April 2014). "Revised surveillance case definition for HIV infection – United States, 2014" (PDF). MMWR. Recommendations and Reports. 63 (RR-03): 1–10. PMID 24717910.
- ^ Crosby R, Bounse S (March 2012). "Condom effectiveness: where are we now?". Sexual Health. 9 (1): 10–17. doi:10.1071/SH11036. PMID 22348628.
- ^ "Condom Facts and Figures". World Health Organization. August 2003. Archived from the original on October 18, 2012. Retrieved January 17, 2006.
- ^ Gallo MF, Kilbourne-Brook M, Coffey PS (March 2012). "A review of the effectiveness and acceptability of the female condom for dual protection". Sexual Health. 9 (1): 18–26. doi:10.1071/SH11037. PMID 22348629.
- ^ a b Celum C, Baeten JM (February 2012). "Tenofovir-based pre-exposure prophylaxis for HIV prevention: evolving evidence". Current Opinion in Infectious Diseases. 25 (1): 51–57. doi:10.1097/QCO.0b013e32834ef5ef. PMC 3266126. PMID 22156901.
- ^ Baptista M, Ramalho-Santos J (November 2009). "Spermicides, microbicides and antiviral agents: recent advances in the development of novel multi-functional compounds". Mini Reviews in Medicinal Chemistry. 9 (13): 1556–67. doi:10.2174/138955709790361548. PMID 20205637.
- ^ Siegfried N, Muller M, Deeks JJ, Volmink J (April 2009). Siegfried N (ed.). "Male circumcision for prevention of heterosexual acquisition of HIV in men". The Cochrane Database of Systematic Reviews (2): CD003362. doi:10.1002/14651858.CD003362.pub2. PMID 19370585.
- ^ "WHO and UNAIDS announce recommendations from expert consultation on male circumcision for HIV prevention". World Health Organization. March 28, 2007. Archived from the original on July 3, 2011.
- ^ Larke N (May 27, 2010). "Male circumcision, HIV and sexually transmitted infections: a review". British Journal of Nursing. 19 (10): 629–34. doi:10.12968/bjon.2010.19.10.48201. PMC 3836228. PMID 20622758.
- ^ Eaton L, Kalichman SC (November 2009). "Behavioral aspects of male circumcision for the prevention of HIV infection". Current HIV/AIDS Reports. 6 (4): 187–93. doi:10.1007/s11904-009-0025-9. PMC 3557929. PMID 19849961.(subscription required)
- ^ Kim HH, Li PS, Goldstein M (November 2010). "Male circumcision: Africa and beyond?". Current Opinion in Urology. 20 (6): 515–19. doi:10.1097/MOU.0b013e32833f1b21. PMID 20844437. S2CID 2158164.
- ^ Templeton DJ, Millett GA, Grulich AE (February 2010). "Male circumcision to reduce the risk of HIV and sexually transmitted infections among men who have sex with men". Current Opinion in Infectious Diseases. 23 (1): 45–52. doi:10.1097/QCO.0b013e328334e54d. PMID 19935420. S2CID 43878584.
- ^ Wiysonge CS, Kongnyuy EJ, Shey M, Muula AS, Navti OB, Akl EA, Lo YR (June 2011). Wiysonge CS (ed.). "Male circumcision for prevention of homosexual acquisition of HIV in men". The Cochrane Database of Systematic Reviews (6): CD007496. doi:10.1002/14651858.CD007496.pub2. PMID 21678366.
- ^ Underhill K, Operario D, Montgomery P (October 2007). Operario D (ed.). "Abstinence-only programs for HIV infection prevention in high-income countries". The Cochrane Database of Systematic Reviews (4): CD005421. doi:10.1002/14651858.CD005421.pub2. PMID 17943855. Archived from the original on November 25, 2010. Retrieved May 31, 2012.
- ^ Tolli MV (October 2012). "Effectiveness of peer education interventions for HIV prevention, adolescent pregnancy prevention and sexual health promotion for young people: a systematic review of European studies". Health Education Research. 27 (5): 904–13. doi:10.1093/her/cys055. PMID 22641791.
- ^ Ljubojević S, Lipozenčić J (2010). "Sexually transmitted infections and adolescence". Acta Dermatovenerologica Croatica. 18 (4): 305–10. PMID 21251451.
- ^ International technical guidance on sexuality education: an evidence-informed approach (PDF). Paris: UNESCO. 2018. p. 12. ISBN 978-92-3-100259-5. Archived (PDF) from the original on November 13, 2018. Retrieved February 22, 2018.
- ^ Patel VL, Yoskowitz NA, Kaufman DR, Shortliffe EH (September 2008). "Discerning patterns of human immunodeficiency virus risk in healthy young adults". The American Journal of Medicine. 121 (9): 758–64. doi:10.1016/j.amjmed.2008.04.022. PMC 2597652. PMID 18724961.
- ^ Fonner VA, Denison J, Kennedy CE, O'Reilly K, Sweat M (September 2012). "Voluntary counseling and testing (VCT) for changing HIV-related risk behavior in developing countries". The Cochrane Database of Systematic Reviews. 9 (9): CD001224. doi:10.1002/14651858.CD001224.pub4. PMC 3931252. PMID 22972050.
- ^ Lopez, LM; Grey, TW; Chen, M; Denison, J; Stuart, G (August 9, 2016). "Behavioral interventions for improving contraceptive use among women living with HIV". The Cochrane Database of Systematic Reviews. 2016 (8): CD010243. doi:10.1002/14651858.CD010243.pub3. PMC 7092487. PMID 27505053.
- ^ a b Anglemyer A, Rutherford GW, Horvath T, Baggaley RC, Egger M, Siegfried N (April 2013). "Antiretroviral therapy for prevention of HIV transmission in HIV-discordant couples". The Cochrane Database of Systematic Reviews. 4 (4): CD009153. doi:10.1002/14651858.CD009153.pub3. PMC 4026368. PMID 23633367.
- ^ Chou R, Selph S, Dana T, Bougatsos C, Zakher B, Blazina I, Korthuis PT (November 2012). "Screening for HIV: systematic review to update the 2005 U.S. Preventive Services Task Force recommendation". Annals of Internal Medicine. 157 (10): 706–18. doi:10.7326/0003-4819-157-10-201211200-00007. PMID 23165662. S2CID 27494096.
- ^ Owens, Douglas K.; Davidson, Karina W.; Krist, Alex H.; Barry, Michael J.; Cabana, Michael; Caughey, Aaron B.; Curry, Susan J.; Doubeni, Chyke A.; Epling, John W.; Kubik, Martha; Landefeld, C. Seth; Mangione, Carol M.; Pbert, Lori; Silverstein, Michael; Simon, Melissa A.; Tseng, Chien-Wen; Wong, John B. (June 11, 2019). "Preexposure Prophylaxis for the Prevention of HIV Infection". JAMA. 321 (22): 2203–2213. doi:10.1001/jama.2019.6390. PMID 31184747.
- ^ Choopanya K, Martin M, Suntharasamai P, Sangkum U, Mock PA, Leethochawalit M, Chiamwongpaet S, Kitisin P, Natrujirote P, Kittimunkong S, Chuachoowong R, Gvetadze RJ, McNicholl JM, Paxton LA, Curlin ME, Hendrix CW, Vanichseni S (June 2013). "Antiretroviral prophylaxis for HIV infection in injecting drug users in Bangkok, Thailand (the Bangkok Tenofovir Study): a randomised, double-blind, placebo-controlled phase 3 trial". The Lancet. 381 (9883): 2083–90. doi:10.1016/S0140-6736(13)61127-7. PMID 23769234. S2CID 5831642.
- ^ US Preventive Services Task, Force.; Owens, DK; Davidson, KW; Krist, AH; Barry, MJ; Cabana, M; Caughey, AB; Curry, SJ; Doubeni, CA; Epling JW, Jr; Kubik, M; Landefeld, CS; Mangione, CM; Pbert, L; Silverstein, M; Simon, MA; Tseng, CW; Wong, JB (June 11, 2019). "Preexposure Prophylaxis for the Prevention of HIV Infection: US Preventive Services Task Force Recommendation Statement". JAMA. 321 (22): 2203–2213. doi:10.1001/jama.2019.6390. PMID 31184747.
- ^ Centers for Disease Control (CDC) (August 1987). "Recommendations for prevention of HIV transmission in health-care settings". MMWR Supplements. 36 (2): 1S–18S. PMID 3112554. Archived from the original on July 9, 2017.
- ^ a b Kurth AE, Celum C, Baeten JM, Vermund SH, Wasserheit JN (March 2011). "Combination HIV prevention: significance, challenges, and opportunities". Current HIV/AIDS Reports. 8 (1): 62–72. doi:10.1007/s11904-010-0063-3. PMC 3036787. PMID 20941553.
- ^ MacArthur GJ, Minozzi S, Martin N, Vickerman P, Deren S, Bruneau J, Degenhardt L, Hickman M (October 2012). "Opiate substitution treatment and HIV transmission in people who inject drugs: systematic review and meta-analysis". BMJ. 345 (oct03 3): e5945. doi:10.1136/bmj.e5945. PMC 3489107. PMID 23038795.
- ^ a b "HIV exposure through contact with body fluids". Prescrire International. 21 (126): 100–01, 103–05. April 2012. PMID 22515138.
- ^ Kuhar DT, Henderson DK, Struble KA, Heneine W, Thomas V, Cheever LW, Gomaa A, Panlilio AL (September 2013). "Updated US Public Health Service guidelines for the management of occupational exposures to human immunodeficiency virus and recommendations for postexposure prophylaxis". Infection Control and Hospital Epidemiology. 34 (9): 875–92. doi:10.1086/672271. PMID 23917901. S2CID 17032413.
- ^ Linden JA (September 2011). "Clinical practice. Care of the adult patient after sexual assault". The New England Journal of Medicine. 365 (9): 834–41. doi:10.1056/NEJMcp1102869. PMID 21879901. S2CID 8388126.
- ^ Young TN, Arens FJ, Kennedy GE, Laurie JW, Rutherford GW (January 2007). Young T (ed.). "Antiretroviral post-exposure prophylaxis (PEP) for occupational HIV exposure". The Cochrane Database of Systematic Reviews. 2012 (1): CD002835. doi:10.1002/14651858.CD002835.pub3. PMC 8989146. PMID 17253483.
- ^ Siegfried N, van der Merwe L, Brocklehurst P, Sint TT (July 2011). Siegfried N (ed.). "Antiretrovirals for reducing the risk of mother-to-child transmission of HIV infection". The Cochrane Database of Systematic Reviews (7): CD003510. doi:10.1002/14651858.CD003510.pub3. PMID 21735394.
- ^ "WHO HIV and Infant Feeding Technical Consultation Held on behalf of the Inter-agency Task Team (IATT) on Prevention of HIV – Infections in Pregnant Women, Mothers and their Infants – Consensus statement" (PDF). October 25–27, 2006. Archived (PDF) from the original on April 9, 2008. Retrieved March 12, 2008.
- ^ Horvath T, Madi BC, Iuppa IM, Kennedy GE, Rutherford G, Read JS (January 2009). Horvath T (ed.). "Interventions for preventing late postnatal mother-to-child transmission of HIV". The Cochrane Database of Systematic Reviews. 2009 (1): CD006734. doi:10.1002/14651858.CD006734.pub2. PMC 7389566. PMID 19160297.
- ^ "WHO validates elimination of mother-to-child transmission of HIV and syphilis in Cuba". World Health Organization. June 30, 2015. Archived from the original on September 4, 2015. Retrieved August 30, 2015.
- ^ Reynell L, Trkola A (March 2012). "HIV vaccines: an attainable goal?". Swiss Medical Weekly. 142: w13535. doi:10.4414/smw.2012.13535. PMID 22389197.
- ^ May MT, Ingle SM (December 2011). "Life expectancy of HIV-positive adults: a review". Sexual Health. 8 (4): 526–33. doi:10.1071/SH11046. PMID 22127039.
- ^ a b UNAIDS 2011 pg. 1–10
- ^ Davis, Nicola (March 8, 2020). "Second Person Ever to Be Cleared of HIV Reveals Identity". The Guardian. Retrieved March 8, 2020.
- ^ "Third person apparently cured of HIV using novel stem cell transplant". TheGuardian.com. February 15, 2022.
- ^ "Man cured of HIV, cancer following breakthrough stem cell transplant: Doctors". ABC News.
- ^ Mateo-Urdiales, Alberto; Johnson, Samuel; Smith, Rhodine; Nachega, Jean B; Eshun-Wilson, Ingrid (June 17, 2019). Cochrane Infectious Diseases Group (ed.). "Rapid initiation of antiretroviral therapy for people living with HIV". Cochrane Database of Systematic Reviews. 6 (6): CD012962. doi:10.1002/14651858.CD012962.pub2. PMC 6575156. PMID 31206168.
- ^ a b c d Antiretroviral therapy for HIV infection in adults and adolescents: recommendations for a public health approach (PDF). World Health Organization. 2010. pp. 19–20. ISBN 978-92-4-159976-4. Archived (PDF) from the original on July 9, 2012.
- ^ a b Consolidated guidelines on the use of antiretroviral drugs for treating and preventing HIV infection (PDF). World Health Organization. 2013. pp. 28–30. ISBN 978-92-4-150572-7. Archived (PDF) from the original on February 9, 2014.
- ^ "UPDATE OF RECOMMENDATIONS ON FIRST- AND SECOND-LINE ANTIRETROVIRAL REGIMENS" (PDF). World Health Organization. July 2019. Retrieved November 16, 2019.
- ^ Marrazzo JM, del Rio C, Holtgrave DR, Cohen MS, Kalichman SC, Mayer KH, Montaner JS, Wheeler DP, Grant RM, Grinsztejn B, Kumarasamy N, Shoptaw S, Walensky RP, Dabis F, Sugarman J, Benson CA (July 23–30, 2014). "HIV prevention in clinical care settings: 2014 recommendations of the International Antiviral Society–USA Panel". JAMA. 312 (4): 390–409. doi:10.1001/jama.2014.7999. PMC 6309682. PMID 25038358.
- ^ "Guidelines for the Use of Antiretroviral Agents in HIV-1-Infected Adults and Adolescents" (PDF). Department of Health and Human Services. February 12, 2013. p. i. Archived (PDF) from the original on November 1, 2016. Retrieved January 3, 2014.
- ^ Sterne JA, May M, Costagliola D, de Wolf F, Phillips AN, Harris R, Funk MJ, Geskus RB, Gill J, Dabis F, Miró JM, Justice AC, Ledergerber B, Fätkenheuer G, Hogg RS, Monforte AD, Saag M, Smith C, Staszewski S, Egger M, Cole SR (April 2009). "Timing of initiation of antiretroviral therapy in AIDS-free HIV-1-infected patients: a collaborative analysis of 18 HIV cohort studies". The Lancet. 373 (9672): 1352–63. doi:10.1016/S0140-6736(09)60612-7. PMC 2670965. PMID 19361855.
- ^ Beard J, Feeley F, Rosen S (November 2009). "Economic and quality of life outcomes of antiretroviral therapy for HIV/AIDS in developing countries: a systematic literature review". AIDS Care. 21 (11): 1343–56. doi:10.1080/09540120902889926. PMID 20024710. S2CID 21883819.
- ^ Attia S, Egger M, Müller M, Zwahlen M, Low N (July 2009). "Sexual transmission of HIV according to viral load and antiretroviral therapy: systematic review and meta-analysis". AIDS. 23 (11): 1397–404. doi:10.1097/QAD.0b013e32832b7dca. PMID 19381076. S2CID 12221693.
- ^ Orrell C (November 2005). "Antiretroviral adherence in a resource-poor setting". Current HIV/AIDS Reports. 2 (4): 171–76. doi:10.1007/s11904-005-0012-8. PMID 16343374. S2CID 44808279.
- ^ Malta M, Strathdee SA, Magnanini MM, Bastos FI (August 2008). "Adherence to antiretroviral therapy for human immunodeficiency virus/acquired immune deficiency syndrome among drug users: a systematic review". Addiction. 103 (8): 1242–57. doi:10.1111/j.1360-0443.2008.02269.x. PMID 18855813.
- ^ Nachega JB, Marconi VC, van Zyl GU, Gardner EM, Preiser W, Hong SY, Mills EJ, Gross R (April 2011). "HIV treatment adherence, drug resistance, virologic failure: evolving concepts". Infectious Disorders Drug Targets. 11 (2): 167–74. doi:10.2174/187152611795589663. PMC 5072419. PMID 21406048.
- ^ Orsi F, d'Almeida C (May 2010). "Soaring antiretroviral prices, TRIPS and TRIPS flexibilities: a burning issue for antiretroviral treatment scale-up in developing countries". Current Opinion in HIV and AIDS. 5 (3): 237–41. doi:10.1097/COH.0b013e32833860ba. PMID 20539080. S2CID 205565246.
- ^ Nachega JB, Mills EJ, Schechter M (January 2010). "Antiretroviral therapy adherence and retention in care in middle-income and low-income countries: current status of knowledge and research priorities". Current Opinion in HIV and AIDS. 5 (1): 70–77. doi:10.1097/COH.0b013e328333ad61. PMID 20046150. S2CID 7491569.
- ^ a b c Montessori V, Press N, Harris M, Akagi L, Montaner JS (January 2004). "Adverse effects of antiretroviral therapy for HIV infection". Canadian Medical Association Journal. 170 (2): 229–38. PMC 315530. PMID 14734438.
- ^ a b c Burgoyne RW, Tan DH (March 2008). "Prolongation and quality of life for HIV-infected adults treated with highly active antiretroviral therapy (HAART): a balancing act". Journal of Antimicrobial Chemotherapy. 61 (3): 469–73. doi:10.1093/jac/dkm499. PMID 18174196.
- ^ Barbaro G, Barbarini G (December 2011). "Human immunodeficiency virus & cardiovascular risk". The Indian Journal of Medical Research. 134 (6): 898–903. doi:10.4103/0971-5916.92634. PMC 3284097. PMID 22310821.
- ^ "Summary of recommendations on when to start ART in children" (PDF). Consolidated ARV guidelines, June 2013. June 2013. Archived (PDF) from the original on October 18, 2014.
- ^ "Guidelines for the Use of Antiretroviral Agents in Pediatric HIV Infection" (PDF). Department of Health and Human Services, February 2014. March 2014. Archived (PDF) from the original on September 14, 2015.
- ^ a b c d "First long-acting injectable antiretroviral therapy for HIV recommended approval". European Medicines Agency (EMA) (Press release). October 16, 2020. Retrieved October 16, 2020. Text was copied from this source which is © European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
- ^ "FDA Approves First Extended-Release, Injectable Drug Regimen for Adults Living with HIV". U.S. Food and Drug Administration (FDA) (Press release). January 21, 2021. Retrieved January 21, 2021. This article incorporates text from this source, which is in the public domain.
- ^ Mandavilli, Apoorva (January 21, 2021). "F.D.A. Approves Monthly Shots to Treat H.I.V." The New York Times. Retrieved January 22, 2021.
- ^ "Guidelines for intensified tuberculosis case-finding and isoniazid preventive therapy for people living with HIV in resource-constrained settings" (PDF). Department of HIV/AIDS, World Health Organization 2011. 2011. Archived (PDF) from the original on October 19, 2014.
- ^ Vonasek, Bryan; Ness, Tara; Takwoingi, Yemisi; Kay, Alexander W; van Wyk, Susanna S; Ouellette, Lara; Marais, Ben J; Steingart, Karen R; Mandalakas, Anna M (June 28, 2021). "Screening tests for active pulmonary tuberculosis in children". Cochrane Database of Systematic Reviews. 2021 (6): CD013693. doi:10.1002/14651858.CD013693.pub2. ISSN 1465-1858. PMC 8237391. PMID 34180536.
- ^ Laurence J (January 2006). "Hepatitis A and B virus immunization in HIV-infected persons". The AIDS Reader. 16 (1): 15–17. PMID 16433468.
- ^ a b UNAIDS 2011 pg. 150–160
- ^ Huang L, Cattamanchi A, Davis JL, den Boon S, Kovacs J, Meshnick S, Miller RF, Walzer PD, Worodria W, Masur H (June 2011). "HIV-associated Pneumocystis pneumonia". Proceedings of the American Thoracic Society. 8 (3): 294–300. doi:10.1513/pats.201009-062WR. PMC 3132788. PMID 21653531.
- ^ "Treating opportunistic infections among HIV-infected adults and adolescents. Recommendations from CDC, the National Institutes of Health, and the HIV Medicine Association/Infectious Diseases Society of America". Department of Health and Human Services. February 2, 2007. Archived from the original on July 27, 2018. Retrieved July 26, 2018.
- ^ a b Smith, Blaine T., ed. (2008). Concepts in immunology and immunotherapeutics (4th ed.). Bethesda, MD: American Society of Health-System Pharmacists. p. 143. ISBN 978-1-58528-127-5. Archived from the original on November 28, 2015. Retrieved June 27, 2015.
- ^ Beck CR, McKenzie BC, Hashim AB, Harris RC, Zanuzdana A, Agboado G, et al. (September 2013). "Influenza vaccination for immunocompromised patients: summary of a systematic review and meta-analysis". Influenza and Other Respiratory Viruses. 7 Suppl 2 (Suppl 2): 72–75. doi:10.1111/irv.12084. PMC 5909396. PMID 24034488.
- ^ Lee KY, Tsai MS, Kuo KC, Tsai JC, Sun HY, Cheng AC, Chang SY, Lee CH, Hung CC (2014). "Pneumococcal vaccination among HIV-infected adult patients in the era of combination antiretroviral therapy". Human Vaccines & Immunotherapeutics. 10 (12): 3700–10. doi:10.4161/hv.32247. PMC 4514044. PMID 25483681.
- ^ a b World Health Organization (May 2003). Nutrient requirements for people living with HIV/AIDS: Report of a technical consultation (PDF). Geneva. Archived from the original (PDF) on March 25, 2009. Retrieved March 31, 2009.
- ^ Forrester JE, Sztam KA (December 2011). "Micronutrients in HIV/AIDS: is there evidence to change the WHO 2003 recommendations?". The American Journal of Clinical Nutrition. 94 (6): 1683S–1689S. doi:10.3945/ajcn.111.011999. PMC 3226021. PMID 22089440.
- ^ Nunnari G, Coco C, Pinzone MR, Pavone P, Berretta M, Di Rosa M, Schnell M, Calabrese G, Cacopardo B (June 2012). "The role of micronutrients in the diet of HIV-1-infected individuals". Frontiers in Bioscience. 4 (7): 2442–56. doi:10.2741/e556. PMID 22652651. Archived from the original on April 16, 2015.
- ^ Zeng L, Zhang L (December 2011). "Efficacy and safety of zinc supplementation for adults, children and pregnant women with HIV infection: systematic review". Tropical Medicine & International Health. 16 (12): 1474–82. doi:10.1111/j.1365-3156.2011.02871.x. PMID 21895892. S2CID 6711255.
- ^ Visser ME, Durao S, Sinclair D, Irlam JH, Siegfried N (May 2017). "Micronutrient supplementation in adults with HIV infection". The Cochrane Database of Systematic Reviews. 2017 (5): CD003650. doi:10.1002/14651858.CD003650.pub4. PMC 5458097. PMID 28518221.
- ^ "HIV and Diabetes". HIVInfo.NIH.gov. Retrieved February 9, 2023.
- ^ Stone CA, Kawai K, Kupka R, Fawzi WW (November 2010). "Role of selenium in HIV infection". Nutrition Reviews. 68 (11): 671–81. doi:10.1111/j.1753-4887.2010.00337.x. PMC 3066516. PMID 20961297.
- ^ a b Siegfried N, Irlam JH, Visser ME, Rollins NN (March 2012). "Micronutrient supplementation in pregnant women with HIV infection". The Cochrane Database of Systematic Reviews (3): CD009755. doi:10.1002/14651858.CD009755. PMID 22419344.
- ^ Irlam JH, Siegfried N, Visser ME, Rollins NC (October 2013). "Micronutrient supplementation for children with HIV infection". The Cochrane Database of Systematic Reviews (10): CD010666. doi:10.1002/14651858.CD010666. PMID 24114375.
- ^ Littlewood RA, Vanable PA (September 2008). "Complementary and alternative medicine use among HIV-positive people: research synthesis and implications for HIV care". AIDS Care. 20 (8): 1002–18. doi:10.1080/09540120701767216. PMC 2570227. PMID 18608078.
- ^ Mills E, Wu P, Ernst E (June 2005). "Complementary therapies for the treatment of HIV: in search of the evidence". International Journal of STD & AIDS. 16 (6): 395–403. doi:10.1258/0956462054093962. PMID 15969772. S2CID 7411052.
- ^ Liu JP, Manheimer E, Yang M (July 2005). Liu JP (ed.). "Herbal medicines for treating HIV infection and AIDS". The Cochrane Database of Systematic Reviews. 2010 (3): CD003937. doi:10.1002/14651858.CD003937.pub2. PMC 8759069. PMID 16034917.
- ^ Lutge EE, Gray A, Siegfried N (April 2013). "The medical use of cannabis for reducing morbidity and mortality in patients with HIV/AIDS". The Cochrane Database of Systematic Reviews. 4 (4): CD005175. doi:10.1002/14651858.CD005175.pub3. PMID 23633327.
- ^ a b c Knoll B, Lassmann B, Temesgen Z (December 2007). "Current status of HIV infection: a review for non-HIV-treating physicians". International Journal of Dermatology. 46 (12): 1219–28. doi:10.1111/j.1365-4632.2007.03520.x. PMID 18173512. S2CID 26248996.
- ^ a b Morgan D, Mahe C, Mayanja B, Okongo JM, Lubega R, Whitworth JA (March 2002). "HIV-1 infection in rural Africa: is there a difference in median time to AIDS and survival compared with that in industrialized countries?". AIDS. 16 (4): 597–603. doi:10.1097/00002030-200203080-00011. PMID 11873003. S2CID 35450422.
- ^ Zwahlen M, Egger M (2006). Progression and mortality of untreated HIV-positive individuals living in resource-limited settings: update of literature review and evidence synthesis (PDF) (Report). UNAIDS Obligation HQ/05/422204. Archived (PDF) from the original on April 9, 2008. Retrieved March 19, 2008.
- ^ a b Antiretroviral Therapy Cohort Collaboration (July 2008). "Life expectancy of individuals on combination antiretroviral therapy in high-income countries: a collaborative analysis of 14 cohort studies". The Lancet. 372 (9635): 293–99. doi:10.1016/S0140-6736(08)61113-7. PMC 3130543. PMID 18657708.
- ^ Schackman BR, Gebo KA, Walensky RP, Losina E, Muccio T, Sax PE, Weinstein MC, Seage GR, Moore RD, Freedberg KA (November 2006). "The lifetime cost of current human immunodeficiency virus care in the United States". Medical Care. 44 (11): 990–97. doi:10.1097/01.mlr.0000228021.89490.2a. PMID 17063130. S2CID 21175266.
- ^ van Sighem AI, Gras LA, Reiss P, Brinkman K, de Wolf F (June 2010). "Life expectancy of recently diagnosed asymptomatic HIV-infected patients approaches that of uninfected individuals". AIDS. 24 (10): 1527–35. doi:10.1097/QAD.0b013e32833a3946. PMID 20467289. S2CID 205987336.
- ^ a b Cheung MC, Pantanowitz L, Dezube BJ (June–July 2005). "AIDS-related malignancies: emerging challenges in the era of highly active antiretroviral therapy". The Oncologist. 10 (6): 412–26. CiteSeerX 10.1.1.561.4760. doi:10.1634/theoncologist.10-6-412. PMID 15967835. S2CID 24329763.
- ^ Tang J, Kaslow RA (2003). "The impact of host genetics on HIV infection and disease progression in the era of highly active antiretroviral therapy". AIDS. 17 Suppl 4 (Suppl 4): S51–60. doi:10.1097/00002030-200317004-00006. PMID 15080180.
- ^ Lawn SD (January 2004). "AIDS in Africa: the impact of coinfections on the pathogenesis of HIV-1 infection". The Journal of Infection. 48 (1): 1–12. doi:10.1016/j.jinf.2003.09.001. PMID 14667787.
- ^ Campbell GR, Pasquier E, Watkins J, Bourgarel-Rey V, Peyrot V, Esquieu D, Barbier P, de Mareuil J, Braguer D, Kaleebu P, Yirrell DL, Loret EP (November 2004). "The glutamine-rich region of the HIV-1 Tat protein is involved in T-cell apoptosis". The Journal of Biological Chemistry. 279 (46): 48197–204. doi:10.1074/jbc.M406195200. PMID 15331610.
- ^ Campbell GR, Watkins JD, Esquieu D, Pasquier E, Loret EP, Spector SA (November 2005). "The C terminus of HIV-1 Tat modulates the extent of CD178-mediated apoptosis of T cells". The Journal of Biological Chemistry. 280 (46): 38376–82. doi:10.1074/jbc.M506630200. PMID 16155003.
- ^ "Tuberculosis". Fact sheet 104. World Health Organization. March 2012. Archived from the original on August 23, 2012. Retrieved August 29, 2012.
- ^ World Health Organization (2011). Global tuberculosis control 2011 (PDF). ISBN 978-92-4-156438-0. Archived from the original (PDF) on September 6, 2012. Retrieved August 29, 2012.
- ^ Rubin R, Strayer DS, Rubin E, eds. (2011). Rubin's pathology: clinicopathologic foundations of medicine (Sixth ed.). Philadelphia: Wolters Kluwer Health/Lippincott Williams & Wilkins. p. 154. ISBN 978-1-60547-968-2. Archived from the original on September 24, 2015. Retrieved June 27, 2015.
- ^ Nelson VM, Benson AB (January 2017). "Epidemiology of Anal Canal Cancer". Surgical Oncology Clinics of North America. 26 (1): 9–15. doi:10.1016/j.soc.2016.07.001. PMID 27889039.
- ^ Woods SP, Moore DJ, Weber E, Grant I (June 2009). "Cognitive neuropsychology of HIV-associated neurocognitive disorders". Neuropsychology Review. 19 (2): 152–68. doi:10.1007/s11065-009-9102-5. PMC 2690857. PMID 19462243.
- ^ Brown TT, Qaqish RB (November 2006). "Antiretroviral therapy and the prevalence of osteopenia and osteoporosis: a meta-analytic review". AIDS. 20 (17): 2165–74. doi:10.1097/QAD.0b013e32801022eb. PMID 17086056. S2CID 19217950.
- ^ Nicholas PK, Kemppainen JK, Canaval GE, Corless IB, Sefcik EF, Nokes KM, Bain CA, Kirksey KM, Eller LS, Dole PJ, Hamilton MJ, Coleman CL, Holzemer WL, Reynolds NR, Portillo CJ, Bunch EH, Wantland DJ, Voss J, Phillips R, Tsai YF, Mendez MR, Lindgren TG, Davis SM, Gallagher DM (February 2007). "Symptom management and self-care for peripheral neuropathy in HIV/AIDS". AIDS Care. 19 (2): 179–89. doi:10.1080/09540120600971083. PMID 17364396. S2CID 30220269.
- ^ Boshoff C, Weiss R (May 2002). "AIDS-related malignancies". Nature Reviews. Cancer. 2 (5): 373–82. doi:10.1038/nrc797. PMID 12044013. S2CID 13513517.
- ^ Yarchoan R, Tosato G, Little RF (August 2005). "Therapy insight: AIDS-related malignancies – the influence of antiviral therapy on pathogenesis and management". Nature Clinical Practice Oncology. 2 (8): 406–15, quiz 423. doi:10.1038/ncponc0253. PMID 16130937. S2CID 23476060.
- ^ Post FA, Holt SG (February 2009). "Recent developments in HIV and the kidney". Current Opinion in Infectious Diseases. 22 (1): 43–48. doi:10.1097/QCO.0b013e328320ffec. PMID 19106702. S2CID 23085633.
- ^ a b Roser, Max; Ritchie, Hannah (April 3, 2018). "HIV / AIDS". Our World in Data. Archived from the original on October 4, 2019. Retrieved October 4, 2019.
- ^ Cohen MS, Hellmann N, Levy JA, DeCock K, Lange J (April 2008). "The spread, treatment, and prevention of HIV-1: evolution of a global pandemic". The Journal of Clinical Investigation. 118 (4): 1244–54. doi:10.1172/JCI34706. PMC 2276790. PMID 18382737.
- ^ a b c "Fact sheet – Latest statistics on the status of the AIDS epidemic | UNAIDS". www.unaids.org. Archived from the original on July 13, 2017. Retrieved July 21, 2017.
- ^ "UNAIDS reports a 52% reduction in new HIV infections among children and a combined 33% reduction among adults and children since 2001". UNAIDS. Archived from the original on October 1, 2013. Retrieved October 7, 2013.
- ^ a b c d UNAIDS 2011 pg. 20–30
- ^ a b c UNAIDS 2011 pp. 40–50
- ^ a b c d Mandell, Bennett, and Dolan (2010). Chapter 117.
- ^ New HIV infections among children have been reduced by 50% or more in seven countries in sub-Saharan Africa Archived June 30, 2013, at the Wayback Machine, UN AIDS, Geneva, June 25, 2013.
- ^ This article incorporates text from this source, which is in the public domain.Centers for Disease Control Prevention (CDC) (June 2011). "HIV surveillance – United States, 1981–2008". Morbidity and Mortality Weekly Report. 60 (21): 689–93. PMID 21637182.
- ^ "Today's HIV/AIDS Epidemic Factsheet" (PDF). Centers for Disease Control and Prevention. Archived (PDF) from the original on December 19, 2016. Retrieved December 31, 2016.
- ^ Public Health England (2016). HIV in the United Kingdom: 2016 Report (PDF). Archived (PDF) from the original on April 25, 2017.
- ^ Surveillance; riques, Risk Assessment Division = Le VIH et le sida au Canada: rapport de surveillance en date du 31 décembre 2009 / Division de la surveillance et de l'évaluation des (2010). HIV and AIDS in Canada: surveillance report to December 31, 2009 (PDF). Ottawa: Public Health Agency of Canada, Centre for Communicable Diseases and Infection Control, Surveillance and Risk Assessment Division. ISBN 978-1-100-52141-1. Archived from the original (PDF) on January 19, 2012.
- ^ "Global Report Fact Sheet" (PDF). UNAIDS. 2010. Archived from the original (PDF) on September 16, 2013.
- ^ "Country Comparison :: HIV/AIDS – Adult Prevalence Rate". CIA World Factbook. Archived from the original on December 21, 2014. Retrieved November 6, 2014.
- ^ "On this day". News & Record. May 18, 2020. p. 2A.
- ^ Cloutier, Bill (May 17, 2020). "Today in History, May 18". Republican-American. Archived from the original on June 1, 2020. Retrieved May 19, 2020.
- ^ "How I told the world about Aids". BBC News. June 5, 2006. Archived from the original on February 12, 2019. Retrieved February 12, 2019.
- ^ Gottlieb MS (June 2006). "Pneumocystis pneumonia – Los Angeles. 1981". American Journal of Public Health. 96 (6): 980–81, discussion 982–83. doi:10.2105/AJPH.96.6.980. PMC 1470612. PMID 16714472. Archived from the original on April 22, 2009.
- ^ Friedman-Kien AE (October 1981). "Disseminated Kaposi's sarcoma syndrome in young homosexual men". Journal of the American Academy of Dermatology. 5 (4): 468–71. doi:10.1016/S0190-9622(81)80010-2. PMID 7287964.
- ^ Hymes KB, Cheung T, Greene JB, Prose NS, Marcus A, Ballard H, William DC, Laubenstein LJ (September 1981). "Kaposi's sarcoma in homosexual men-a report of eight cases". The Lancet. 2 (8247): 598–600. doi:10.1016/S0140-6736(81)92740-9. PMID 6116083. S2CID 43529542.
- ^ a b Basavapathruni A, Anderson KS (December 2007). "Reverse transcription of the HIV-1 pandemic". FASEB Journal. 21 (14): 3795–808. doi:10.1096/fj.07-8697rev. PMID 17639073. S2CID 24960391.
- ^ Centers for Disease Control (CDC) (May 1982). "Persistent, generalized lymphadenopathy among homosexual males". Morbidity and Mortality Weekly Report. 31 (19): 249–51. PMID 6808340. Archived from the original on October 18, 2011.
- ^ a b Barré-Sinoussi F, Chermann JC, Rey F, Nugeyre MT, Chamaret S, Gruest J, Dauguet C, Axler-Blin C, Vézinet-Brun F, Rouzioux C, Rozenbaum W, Montagnier L (May 1983). "Isolation of a T-lymphotropic retrovirus from a patient at risk for acquired immune deficiency syndrome (AIDS)". Science. 220 (4599): 868–71. Bibcode:1983Sci...220..868B. doi:10.1126/science.6189183. PMID 6189183. S2CID 390173.
- ^ a b Centers for Disease Control (CDC) (July 1982). "Opportunistic infections and Kaposi's sarcoma among Haitians in the United States". Morbidity and Mortality Weekly Report. 31 (26): 353–54, 360–61. PMID 6811853. Archived from the original on September 20, 2011.
- ^ Gilman, Sander L (1987). Gilman, Sander L. (ed.). "AIDS and Syphilis: The Iconography of Disease". October. 43: 87–107. doi:10.2307/3397566. JSTOR 3397566.
- ^ "Making Headway Under Hellacious Circumstances" (PDF). American Association for the Advancement of Science. July 28, 2006. Archived (PDF) from the original on June 24, 2008. Retrieved June 23, 2008.
- ^ Altman LK (May 11, 1982). "New homosexual disorder worries health officials". The New York Times. Archived from the original on April 30, 2013. Retrieved August 31, 2011.
- ^ Kher U (July 27, 1982). "A Name for the Plague". Time. Archived from the original on March 7, 2008. Retrieved March 10, 2008.
- ^ Centers for Disease Control (CDC) (September 1982). "Update on acquired immune deficiency syndrome (AIDS) – United States". Morbidity and Mortality Weekly Report. 31 (37): 507–08, 513–14. PMID 6815471.
- ^ Gallo RC, Sarin PS, Gelmann EP, Robert-Guroff M, Richardson E, Kalyanaraman VS, Mann D, Sidhu GD, Stahl RE, Zolla-Pazner S, Leibowitch J, Popovic M (May 1983). "Isolation of human T-cell leukemia virus in acquired immune deficiency syndrome (AIDS)". Science. 220 (4599): 865–67. Bibcode:1983Sci...220..865G. doi:10.1126/science.6601823. PMID 6601823.
- ^ Aldrich R, Wotherspoon G, eds. (2001). Who's who in gay and lesbian history. London: Routledge. p. 154. ISBN 978-0-415-22974-6. Archived from the original on September 11, 2015. Retrieved June 27, 2015.
- ^ a b c Gilbert MT, Rambaut A, Wlasiuk G, Spira TJ, Pitchenik AE, Worobey M (November 2007). "The emergence of HIV/AIDS in the Americas and beyond". Proceedings of the National Academy of Sciences of the United States of America. 104 (47): 18566–70. Bibcode:2007PNAS..10418566G. doi:10.1073/pnas.0705329104. PMC 2141817. PMID 17978186.
- ^ Gao F, Bailes E, Robertson DL, Chen Y, Rodenburg CM, Michael SF, Cummins LB, Arthur LO, Peeters M, Shaw GM, Sharp PM, Hahn BH (February 1999). "Origin of HIV-1 in the chimpanzee Pan troglodytes troglodytes". Nature. 397 (6718): 436–41. Bibcode:1999Natur.397..436G. doi:10.1038/17130. PMID 9989410. S2CID 4432185.
- ^ Keele BF, Van Heuverswyn F, Li Y, Bailes E, Takehisa J, Santiago ML, Bibollet-Ruche F, Chen Y, Wain LV, Liegeois F, Loul S, Ngole EM, Bienvenue Y, Delaporte E, Brookfield JF, Sharp PM, Shaw GM, Peeters M, Hahn BH (July 2006). "Chimpanzee reservoirs of pandemic and nonpandemic HIV-1". Science. 313 (5786): 523–26. Bibcode:2006Sci...313..523K. doi:10.1126/science.1126531. PMC 2442710. PMID 16728595.
- ^ Goodier JL, Kazazian HH (October 2008). "Retrotransposons revisited: the restraint and rehabilitation of parasites". Cell. 135 (1): 23–35. doi:10.1016/j.cell.2008.09.022. PMID 18854152. S2CID 3093360.(subscription required)
- ^ Sharp PM, Bailes E, Chaudhuri RR, Rodenburg CM, Santiago MO, Hahn BH (June 2001). "The origins of acquired immune deficiency syndrome viruses: where and when?". Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 356 (1410): 867–76. doi:10.1098/rstb.2001.0863. PMC 1088480. PMID 11405934.
- ^ Kalish ML, Wolfe ND, Ndongmo CB, McNicholl J, Robbins KE, Aidoo M, Fonjungo PN, Alemnji G, Zeh C, Djoko CF, Mpoudi-Ngole E, Burke DS, Folks TM (December 2005). "Central African hunters exposed to simian immunodeficiency virus". Emerging Infectious Diseases. 11 (12): 1928–30. doi:10.3201/eid1112.050394. PMC 3367631. PMID 16485481.
- ^ a b Marx PA, Alcabes PG, Drucker E (June 2001). "Serial human passage of simian immunodeficiency virus by unsterile injections and the emergence of epidemic human immunodeficiency virus in Africa". Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 356 (1410): 911–20. doi:10.1098/rstb.2001.0867. PMC 1088484. PMID 11405938.
- ^ Worobey M, Gemmel M, Teuwen DE, Haselkorn T, Kunstman K, Bunce M, Muyembe JJ, Kabongo JM, Kalengayi RM, Van Marck E, Gilbert MT, Wolinsky SM (October 2008). "Direct evidence of extensive diversity of HIV-1 in Kinshasa by 1960". Nature. 455 (7213): 661–64. Bibcode:2008Natur.455..661W. doi:10.1038/nature07390. PMC 3682493. PMID 18833279. (subscription required)
- ^ a b de Sousa JD, Müller V, Lemey P, Vandamme AM (April 2010). Martin DP (ed.). "High GUD incidence in the early 20th century created a particularly permissive time window for the origin and initial spread of epidemic HIV strains". PLOS One. 5 (4): e9936. Bibcode:2010PLoSO...5.9936S. doi:10.1371/journal.pone.0009936. PMC 2848574. PMID 20376191.
- ^ Chitnis A, Rawls D, Moore J (January 2000). "Origin of HIV type 1 in colonial French Equatorial Africa?". AIDS Research and Human Retroviruses. 16 (1): 5–8. doi:10.1089/088922200309548. PMID 10628811. S2CID 17783758.(subscription required)
- ^ Donald G. McNeil Jr. (September 16, 2010). "Precursor to H.I.V. Was in Monkeys for Millennia". The New York Times. Archived from the original on May 11, 2011. Retrieved September 17, 2010.
Dr. Marx believes that the crucial event was the introduction into Africa of millions of inexpensive, mass-produced syringes in the 1950s. ... suspect that the growth of colonial cities is to blame. Before 1910, no Central African town had more than 10,000 people. But urban migration rose, increasing sexual contacts and leading to red-light districts.
- ^ Zhu T, Korber BT, Nahmias AJ, Hooper E, Sharp PM, Ho DD (February 1998). "An African HIV-1 sequence from 1959 and implications for the origin of the epidemic". Nature. 391 (6667): 594–97. Bibcode:1998Natur.391..594Z. doi:10.1038/35400. PMID 9468138. S2CID 4416837.
- ^ "Forty years after first documented AIDS cases, survivors reckon with 'dichotomy of feelings'". NBC News. Retrieved June 6, 2021.
- ^ Lederberg J, ed. (2000). Encyclopedia of Microbiology (2nd ed.). Burlington, MA: Elsevier. p. 106. ISBN 978-0-08-054848-7. Archived from the original on September 10, 2017. Retrieved December 12, 2016.
- ^ Jackson, Regine O., ed. (2011). Geographies of the Haitian Diaspora. Routledge. p. 12. ISBN 978-0-415-88708-3. Archived from the original on May 9, 2016. Retrieved March 13, 2016.
- ^ a b Pépin, Jacques (2011). The Origin of Aids. Cambridge University Press. p. 188. ISBN 978-0-521-18637-7. Archived from the original on May 9, 2016. Retrieved March 13, 2016.
- ^ Kolata, Gina (October 28, 1987). "Boy's 1969 Death Suggests AIDS Invaded U.S. Several Times". The New York Times. Archived from the original on February 11, 2009. Retrieved February 11, 2009.
- ^ "Ryan White, an American AIDS Victim". Encyclopædia Britannica. November 7, 2013. Archived from the original on July 22, 2015. Retrieved July 16, 2015.
- ^ Ogden J, Nyblade L (2005). "Common at its core: HIV-related stigma across contexts" (PDF). International Center for Research on Women. Archived from the original (PDF) on February 17, 2007. Retrieved February 15, 2007.
- ^ a b c Herek GM, Capitanio JP (1999). "AIDS Stigma and sexual prejudice" (PDF). American Behavioral Scientist. 42 (7): 1130–47. doi:10.1177/0002764299042007006. S2CID 143508360. Archived from the original (PDF) on April 9, 2006. Retrieved March 27, 2006.
- ^ Snyder M, Omoto AM, Crain AL (1999). "Punished for their good deeds: stigmatization for AIDS volunteers". American Behavioral Scientist. 42 (7): 1175–92. doi:10.1177/0002764299042007009. S2CID 144929159.
- ^ Sharma, A.K. (2012). Population and society. New Delhi: Concept Pub. Co. p. 242. ISBN 978-81-8069-818-7. Archived from the original on September 24, 2015. Retrieved June 27, 2015.
- ^ Herek GM, Capitanio JP, Widaman KF (March 2002). "HIV-related stigma and knowledge in the United States: prevalence and trends, 1991–1999". American Journal of Public Health. 92 (3): 371–77. doi:10.2105/AJPH.92.3.371. PMC 1447082. PMID 11867313.
- ^ De Cock KM, Jaffe HW, Curran JW (June 2012). "The evolving epidemiology of HIV/AIDS". AIDS. 26 (10): 1205–13. doi:10.1097/QAD.0b013e328354622a. PMID 22706007. S2CID 30648421.
- ^ Smith, Kristen (June 1, 2015). "Rent: Constructing community". International Journal of Media & Cultural Politics. 11 (2): 225–238. doi:10.1386/macp.11.2.225_1. ISSN 1740-8296.
- ^ Richard Spencer (August 21, 2003). "China relaxes laws on love and marriage". The Telegraph. Archived from the original on November 8, 2013. Retrieved October 24, 2013.
- ^ "Exhibition – Surviving and Thriving – NLM Exhibition Program". www.nlm.nih.gov. U.S. National Institutes of Health, National Library of Medicine. Archived from the original on December 1, 2017. Retrieved March 16, 2018.
- ^ Geiling, Natasha (December 4, 2013). "The Confusing and At-Times Counterproductive 1980s Response to the AIDS Epidemic". Smithsonian.com. Archived from the original on March 16, 2018. Retrieved March 16, 2018.
- ^ Bell C, Devarajan S, Gersbach H (2003). The long-run economic costs of AIDS: theory and an application to South Africa (Report). World Bank Policy Research Working Paper No. 3152. Archived from the original (PDF) on June 5, 2013. Retrieved April 28, 2008.
- ^ a b Greener R (2002). "AIDS and macroeconomic impact" (PDF). In Forsyth S (ed.). State of The Art: AIDS and Economics. IAEN. pp. 49–55. Archived (PDF) from the original on October 12, 2012.
- ^ Robinson R, Okpo E, Mngoma N (May 2015). "Interventions for improving employment outcomes for workers with HIV". The Cochrane Database of Systematic Reviews. 5 (5): CD010090. doi:10.1002/14651858.CD010090.pub2. hdl:2164/6021. PMID 26022149.
- ^ Over M (1992). The macroeconomic impact of AIDS in Sub-Saharan Africa, Population and Human Resources Department (PDF) (Report). World Bank. Archived (PDF) from the original on May 27, 2008. Retrieved May 3, 2008.
- ^ "AIDS Stigma". News-medical.net. December 7, 2009. Archived from the original on November 12, 2011. Retrieved November 1, 2011.
- ^ a b "Thirty years after AIDS discovery, appreciation growing for Catholic approach". Catholicnewsagency.com. June 5, 2011. Archived from the original on October 16, 2011. Retrieved November 1, 2011.
- ^ a b "Church HIV prayer cure claims 'cause three deaths'". BBC News. October 18, 2011. Archived from the original on October 18, 2011. Retrieved October 18, 2011.
- ^ Berger, Joseph (October 3, 1985). "Rock Hudson, Screen Idol, Dies at 59". The New York Times. Retrieved November 6, 2022.
- ^ Coleman, Brian (June 25, 2007). "Thatcher the gay icon". New Statesman. Archived from the original on November 14, 2011. Retrieved November 1, 2011.
- ^ "November 24, 1991: Giant of rock dies". BBC On This Day. BBC News. November 24, 1991. Archived from the original on October 21, 2011. Retrieved November 1, 2011.
- ^ Bliss, Dominic. "Frozen In Time: Arthur Ashe". iTENNISstore.com. Archived from the original on July 30, 2013. Retrieved June 25, 2012.
- ^ "Tributes to Arthur Ashe". The Independent. London. February 8, 1993. Archived from the original on November 11, 2012. Retrieved July 24, 2012.
- ^ Cosgrove, Ben. "Behind the Picture: The Photo That Changed the Face of AIDS". LIFE magazine. Archived from the original on August 14, 2012. Retrieved August 16, 2012.
- ^ "Germany's most famous gay rights activist: Rosa von Praunheim". Deutsche Welle. Retrieved June 14, 2018.
- ^ "HIV-Specific Criminal Laws". cdc.gov. June 30, 2014. Archived from the original on October 31, 2014. Retrieved November 22, 2014.
- ^ "Aziga found guilty of first-degree murder". CTV.ca News. April 4, 2009. Archived from the original on October 29, 2013. Retrieved April 9, 2013.
- ^ "HIV killer ruled dangerous offender". CBC News. Archived from the original on September 3, 2012. Retrieved April 9, 2013.
- ^ "A fraudster, not a murderer". National Post. March 30, 2010. Archived from the original on May 15, 2016. Retrieved April 9, 2013.
- ^ "'Virgin cure': Three women killed to 'cure' Aids". International Herald Tribune. February 28, 2013. Archived from the original on October 15, 2013. Retrieved September 14, 2013.
- ^ Jenny, Carole (2010). Child Abuse and Neglect: Diagnosis, Treatment and Evidence – Expert Consult. Elsevier Health Sciences. p. 187. ISBN 978-1-4377-3621-2. Archived from the original on November 27, 2015. Retrieved June 27, 2015.
- ^ Klot, Jennifer; Monica Kathina Juma (2011). HIV/AIDS, Gender, Human Security and Violence in Southern Africa. Pretoria: Africa Institute of South Africa. p. 47. ISBN 978-0-7983-0253-1. Archived from the original on April 26, 2016. Retrieved June 27, 2015.
- ^ Ukockis, Gail (2016). Women's Issues for a New Generation: A Social Work Perspective. Oxford University Press. p. 407. ISBN 978-0190239404.
- ^ Glazzard, Jonathan; Stones, Samuel (2020). Relationships and Sex Education for Secondary Schools (2020): A Practical Toolkit for Teachers. Critical Publishing. p. 87. ISBN 978-1913063689.
- ^ "HIV Public Knowledge and Attitudes 2014" (PDF). National AIDS Trust. November 2014. p. 9. Archived from the original (PDF) on February 12, 2015. Retrieved February 12, 2015.
- ^ Blechner MJ (1997). Hope and mortality: psychodynamic approaches to AIDS and HIV. Hillsdale, NJ: Analytic Press. ISBN 978-0-88163-223-1.
- ^ Kirby DB, Laris BA, Rolleri LA (March 2007). "Sex and HIV education programs: their impact on sexual behaviors of young people throughout the world". The Journal of Adolescent Health. 40 (3): 206–17. doi:10.1016/j.jadohealth.2006.11.143. PMID 17321420.
- ^ Duesberg P (July 1988). "HIV is not the cause of AIDS". Science. 241 (4865): 514, 517. Bibcode:1988Sci...241..514D. doi:10.1126/science.3399880. PMID 3399880.Cohen J (December 1994). "The Duesberg phenomenon" (PDF). Science. 266 (5191): 1642–44. Bibcode:1994Sci...266.1642C. doi:10.1126/science.7992043. PMID 7992043. Archived from the original (PDF) on January 1, 2007.
- ^ Kalichman, Seth (2009). Denying AIDS: Conspiracy Theories, Pseudoscience, and Human Tragedy. New York: Copernicus Books (Springer Science+Business Media). ISBN 978-0-387-79475-4.
- ^ Smith TC, Novella SP (August 2007). "HIV denial in the Internet era". PLOS Medicine. 4 (8): e256. doi:10.1371/journal.pmed.0040256. PMC 1949841. PMID 17713982.
- ^ Various (January 14, 2010). "Resources and Links, HIV-AIDS Connection". National Institute of Allergy and Infectious Diseases. Archived from the original on April 7, 2010. Retrieved February 22, 2009.
- ^ Watson J (January 2006). "Scientists, activists sue South Africa's AIDS 'denialists'". Nature Medicine. 12 (1): 6. doi:10.1038/nm0106-6a. PMID 16397537. S2CID 3502309.
- ^ Baleta A (March 2003). "S Africa's AIDS activists accuse government of murder". The Lancet. 361 (9363): 1105. doi:10.1016/S0140-6736(03)12909-1. PMID 12672319. S2CID 43699468.
- ^ Cohen J (June 2000). "South Africa's new enemy". Science. 288 (5474): 2168–70. doi:10.1126/science.288.5474.2168. PMID 10896606. S2CID 2844528.
- ^ Boghardt, Thomas (2009). "Operation INFEKTION Soviet Bloc Intelligence and Its AIDS Disinformation Campaign". Central Intelligence Agency. Archived from the original on May 14, 2011.
- ^ "Video Resurfaces of Fauci Warning 'Household Contact' with AIDS Patients Could Put Kids at Risk". November 9, 2021.
- ^ "Indicators – Program Evaluation – CDC". www.cdc.gov. Archived from the original on August 23, 2018. Retrieved August 24, 2018.
- ^ "Community-Based Indicators for HIV Programs – MEASURE Evaluation". www.measureevaluation.org. Archived from the original on August 25, 2018. Retrieved August 24, 2018.
- ^ "Data and statistics". World Health Organization. Archived from the original on September 2, 2018. Retrieved August 24, 2018.
- Mandell, Gerald L.; Bennett, John E.; Dolin, Raphael, eds. (2010). Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases (7th ed.). Philadelphia, PA: Churchill Livingstone/Elsevier. ISBN 978-0-443-06839-3.
- Joint United Nations Programme on HIV/AIDS (UNAIDS) (2011). Global HIV/AIDS Response, Epidemic update and health sector progress towards universal access (PDF). Joint United Nations Programme on HIV/AIDS.
- HIV/AIDS at Curlie
- UNAIDS – Joint United Nations Program on HIV/AIDS
- HIVinfo – Information on HIV/AIDS treatment, prevention, and research, U.S. Department of Health and Human Services
- 2018 Recommendations of the International Antiviral Society