Jump to content

Vaccine: Difference between revisions

Edit links
From Wikipedia, the free encyclopedia
Browse history interactively
← Previous editNext edit →
Content deleted Content added
VisualWikitext
Go back on some of those edits; for example, Jenner wrote "cow pox" not "cowpox".
m Resized references per Template:Reflist#Browser support and Wikipedia:Footnotes#Resizing references, so smaller size will be reflected in IE7
Line 140: Line 140:


==References==
==References==
<div class="references-small"><references /></div>
{{reflist|colwidth=30em}}


==External links==
==External links==
Line 147: Line 147:
* [http://www.violinet.org/ VIOLIN]: Vaccine Investigation and Online Information Network
* [http://www.violinet.org/ VIOLIN]: Vaccine Investigation and Online Information Network



<!--Use two spaces after External links section, so navboxes don't bunch up. -->
{{Vaccines}}
{{Vaccines}}
{{Major Drug Groups}}
{{Major Drug Groups}}

Revision as of 21:15, 16 December 2008

For other uses, see Vaccine (disambiguation).

A vaccine is a biological preparation that establishes or improves immunity to a particular disease.

Vaccines can be prophylactic (e.g. to prevent or ameliorate the effects of a future infection by any natural or "wild" pathogen), or therapeutic (e.g. vaccines against cancer are also being investigated; see cancer vaccine).

The term vaccine derives from Edward Jenner's 1796 use of the term cow pox (Latin variolæ vaccinæ, adapted from the Latin vaccīn-us, from vacca cow), which, when administered to humans, provided them protection against smallpox.

History

The early vaccines were inspired by the concept of variolation originating in China, in which a person is deliberately infected with a weak form of smallpox as a form of inoculation. Jenner observed that milkmaids who had contact with cowpox did not get smallpox. He discovered that deliberate vaccination with cowpox (which has very mild effect in humans) would prevent smallpox (which is often fatal). Jenner's work was continued by Louis Pasteur and others in the 19th century. Since vaccination against smallpox was much safer than smallpox inoculation, the latter fell into disuse and was eventually banned in England in 1849.

The 19th and 20th centuries saw the introduction of several successful vaccines against a number of infectious diseases. These included bacterial and viral diseases, but not (to date) any parasitic diseases.

Types

Avian flu vaccine development by reverse genetics techniques.

Vaccines may be dead or inactivated organisms or purified products derived from them.

There are four types of traditional vaccines:[1]

  • Vaccines containing killed microorganisms - these are previously virulent micro-organisms which have been killed with chemicals or heat. Examples are vaccines against flu, cholera, bubonic plague, and hepatitis A.
  • Vaccines containing live, attenuated virus microorganisms - these are live micro-organisms that have been cultivated under conditions that disable their virulent properties or which use closely-related but less dangerous organisms to produce a broad immune response. They typically provoke more durable immunological responses and are the preferred type for healthy adults. Examples include yellow fever, measles, rubella, and mumps. The live tuberculosis vaccine is not the contagious strain, but a related strain called "BCG"; it is used in the United States very infrequently.
  • Toxoids - these are inactivated toxic compounds in cases where these (rather than the micro-organism itself) cause illness. Examples of toxoid-based vaccines include tetanus and diphtheria. Not all toxoids are for micro-organisms; for example, Crotalis atrox toxoid is used to vaccinate dogs against rattlesnake bites.
  • Protein subunit - rather than introducing an inactivated or attenuated micro-organism to an immune system (which would constitute a "whole-agent" vaccine), a fragment of it can create an immune response. Characteristic examples include the subunit vaccine against Hepatitis B virus that is composed of only the surface proteins of the virus (produced in yeast) and the virus-like particle (VLP) vaccine against human papillomavirus (HPV) that is composed of the viral major capsid protein.

A number of innovative vaccines are also in development and in use:

  • Conjugate - certain bacteria have polysaccharide outer coats that are poorly immunogenic. By linking these outer coats to proteins (e.g. toxins), the immune system can be led to recognize the polysaccharide as if it were a protein antigen. This approach is used in the Haemophilus influenzae type B vaccine.
  • Recombinant Vector - by combining the physiology of one micro-organism and the DNA of the other, immunity can be created against diseases that have complex infection processes
  • DNA vaccination - in recent years a new type of vaccine, created from an infectious agent's DNA called DNA vaccination, has been developed. It works by insertion (and expression, triggering immune system recognition) into human or animal cells, of viral or bacterial DNA. Some cells of the immune system that recognize the proteins expressed will mount an attack against these proteins and cells expressing them. Because these cells live for a very long time, if the pathogen that normally expresses these proteins is encountered at a later time, they will be attacked instantly by the immune system. One advantage of DNA vaccines is that they are very easy to produce and store. As of 2006, DNA vaccination is still experimental.

While most vaccines are created using inactivated or attenuated compounds from micro-organisms, synthetic vaccines are composed mainly or wholly of synthetic peptides, carbohydrates or antigens.

Vaccines may be monovalent (also called univalent) or multivalent (also called polyvalent). A monovalent vaccine is designed to immunize against a single antigen or single microorganism.[2] A multivalent or polyvalent vaccine is designed to immunize against two or more strains of the same microorganism, or against two or more microorganisms.[3] In certain cases a monovalent vaccine may be preferable for rapidly developing a strong immune response.[4]

Developing immunity

The immune system recognizes vaccine agents as foreign, destroys them, and 'remembers' them. When the virulent version of an agent comes along the body recognises the protein coat on the virus, and thus is prepared to respond, by (1) neutralizing the target agent before it can enter cells, and (2) by recognizing and destroying infected cells before that agent can multiply to vast numbers.

Vaccines have contributed to the eradication of smallpox, one of the most contagious and deadly diseases known to man. Other diseases such as rubella, polio, measles, mumps, chickenpox, and typhoid are nowhere near as common as they were a hundred years ago. As long as the vast majority of people are vaccinated, it is much more difficult for an outbreak of disease to occur, let alone spread. This effect is called herd immunity. Polio, which is transmitted only between humans, is targeted by an extensive eradication campaign that has seen endemic polio restricted to only parts of four countries.[1] The difficulty of reaching all children as well as cultural misunderstandings, however, have caused the anticipated eradication date to be missed several times.

Schedule

Main article: Vaccination schedule
See also: Vaccination policy

In order to provide best protection, children are recommended to receive vaccinations as soon as their immune systems are sufficiently developed to respond to particular vaccines, with additional 'booster' shots often required to achieve 'full immunity'. This has led to the development of complex vaccination schedules. In the United States, the Advisory Committee on Immunization Practices, which recommends schedule additions for the Centers for Disease Control and Prevention, recommends routine vaccination of children against: hepatitis A, hepatitis B, polio, mumps, measles, rubella, diphtheria, pertussis, tetanus, HiB, chickenpox, rotavirus, influenza, meningococcal disease and pneumonia. The large number of vaccines and boosters recommended (up to 24 injections by age two) has led to problems with achieving full compliance. In order to combat declining compliance rates, various notification systems have been instituted and a number of combination injections are now marketed (e.g., Pneumococcal conjugate vaccine and MMRV vaccine), which provide protection against multiple diseases.

Besides recommendations for infant vaccinations and boosters, many specific vaccines are recommended at other ages or for repeated injections throughout life -- most commonly for measles, tetanus, influenza, and pneumonia. Pregnant women are often screened for continued resistance to rubella. The human papillomavirus vaccine is currently recommended in the U.S. and UK for ages 11–25. Vaccine recommendations for the elderly concentrate on pneumonia and influenza, which are more deadly to that group. In 2006, a vaccine was introduced against shingles, a disease caused by the chickenpox virus, which usually affects the elderly.

In Australia, a massive increase in vaccination rates was observed when the federal government made certain benefits (such as the universal 'Family Allowance' welfare payments for parents of children) dependent upon vaccination compliance. As well, children were not allowed into school unless they were either vaccinated or their parents completed a statutory declaration refusing to immunize them, after discussion with a doctor, and other bureaucracy. (Similar school-entry vaccination regulations have been in place in some parts of Canada for several years.) It became easier and cheaper to vaccinate one's children than not to. When faced with the annoyance, many more casual objectors simply gave in.[citation needed]

Efficacy

Vaccines do not guarantee complete protection from a disease. Sometimes this is because the host's immune system simply doesn't respond adequately or at all. This may be due to a lowered immunity in general (diabetes, steroid use, HIV infection) or because the host's immune system does not have a B cell capable of generating antibodies to that antigen.

Even if the host develops antibodies, the human immune system is not perfect and in any case the immune system might still not be able to defeat the infection.

Adjuvants are typically used to boost immune response. Adjuvants are sometimes called the dirty little secret of vaccines [2] in the scientific community, as not much is known about how adjuvants work. Most often aluminium adjuvants are used, but adjuvants like squalene are also used in some vaccines and more vaccines with squalene and phosphate adjuvants are being tested. The efficacy or performance of the vaccine is dependent on a number of factors:

  • the disease itself (for some diseases vaccination performs better than for other diseases)
  • the strain of vaccine (some vaccinations are for different strains of the disease) [3]
  • whether one kept to the timetable for the vaccinations (see Vaccination schedule)
  • some individuals are 'non-responders' to certain vaccines, meaning that they do not generate antibodies even after being vaccinated correctly
  • other factors such as ethnicity or genetic predisposition

When a vaccinated individual does develop the disease vaccinated against, the disease is likely to be milder than without vaccination.

The following are important considerations in the effectiveness of a vaccination program:[citation needed]

  1. careful modelling to anticipate the impact that an immunisation campaign will have on the epidemiology of the disease in the medium to long term
  2. ongoing surveillance for the relevant disease following introduction of a new vaccine and
  3. maintaining high immunisation rates, even when a disease has become rare.

In 1958 there were 763,094 cases of measles and 552 deaths in the United States.[5][6] With the help of new vaccines, the number of cases dropped to fewer than 150 per year (median of 56).[6] In early 2008, there were 64 suspected cases of measles. 54 out of 64 infections were associated with importation from another country, although only 13% were actually acquired outside of the United States; 63 of these 64 individuals either had never been vaccinated against measles, or were uncertain whether they had been vaccinated.[6]

Types of vaccine developments

  • Rational attenuation. Specific modifications or deletions of genes that confer virulence reduce or remove the pathogenicity of the microbe while still allowing an immune response to be generated. This type of rational attenuation can be viewed as creating a "live" attenuated vaccine.
  • Vector-mediated subunit delivery. Introducing a non-infectious, non-pathogenic subunit into a live vector can prompt an immune response without presence of the pathogen. This is called vector-mediated subunit delivery. For example, rabies surface protein gene has been inserted into vaccinia virus.
  • Virus-like particles. Capsid proteins of icosahedral viruses assemble without the presence of a genome. These virus-like particles are antigenically authentic, but non-infectious. This has been used for HPV-16 and HPV-18 vaccines.
  • InVacc-platform is another advance on the original DNA vaccines and generates new vaccines with greatly enhanced properties. The platform consists of a chain of amino acids inserted into the adenovirus, which ensures that more of the antigens are shown to the immune system.[7]

Controversy

James Gillray, The Cow-Pock—or—the Wonderful Effects of the New Inoculation! (1802)
Main article: Vaccine controversy

Opposition to vaccination, from a wide array of vaccine critics, has existed since the earliest vaccination campaigns.[8] Disputes have arisen over the morality, ethics, effectiveness, and safety of vaccination. The mainstream medical opinion is that the benefits of preventing suffering and death from serious infectious diseases greatly outweigh the risks of rare adverse effects following immunization.[9][10] Some vaccination critics say that vaccines are ineffective against disease[11] or that vaccine safety studies are inadequate.[10][11] Some religious groups do not allow vaccination,[12] and some political groups oppose mandatory vaccination on the grounds of individual liberty.[8]

Economics of development

One challenge in vaccine development is economic: many of the diseases most demanding a vaccine, including HIV, malaria and tuberculosis, exist principally in poor countries. Pharmaceutical firms and biotechnology companies have little incentive to develop vaccines for these diseases, because there is little revenue potential. Even in more affluent countries, financial returns are usually minimal and the financial and other risks are great.[13]

Most vaccine development to date has relied on 'push' funding by government, universities and non-profit organizations.[citation needed] Many vaccines have been highly cost effective and beneficial for public health.[13] The number of vaccines actually administered has risen dramatically in recent decades. This increase, particularly in the number of different vaccines administered to children before entry into schools may be due to government mandates and support, rather than economic incentive.[citation needed]

Many researchers and policymakers are calling for a different approach, using 'pull' mechanisms to motivate industry. Mechanisms such as prizes, tax credits, or advance market commitments could ensure a financial return to firms that successfully developed a HIV vaccine. If the policy were well-designed, it might also ensure people have access to a vaccine if and when it is developed.[citation needed]

Intellectual property

Intellectual property can also be viewed as an obstacle to the development of new vaccines. Because of the weak protection offered through the patent of the final product, the protection of the innovation regarding vaccines is often made through the patent of processes used on the development of new vaccines as well as the protection of secrecy.[14]

Preservatives

Many vaccines need preservatives to prevent serious adverse effects such as the Staphylococcus infection that, in one 1928 incident, killed 12 of 21 children inoculated with a diphtheria vaccine that lacked a preservative.[15] Several preservatives are available, including thiomersal, phenoxyethanol, and formaldehyde. Thiomersal is more effective against bacteria, has better shelf life, and improves vaccine stability, potency, and safety, but in the U.S., the European Union, and a few other affluent countries, it is no longer used as a preservative in childhood vaccines, as a precautionary measure due to its mercury content.[16] Controversial claims have been made that thiomersal contributes to autism; no convincing scientific evidence supports these claims.[17]

Delivery systems

There are several new delivery systems in development, which will hopefully make vaccines more efficient to deliver. Possible methods include liposomes and ISCOM (immune stimulating complex).[18]

The latest developments in vaccine delivery technologies have resulted in oral vaccines. A polio vaccine was developed and tested by volunteer vaccinations with no formal training; the results were very positive in that the ease of the vaccines increased dramatically. With an oral vaccine, there is no risk of blood contamination. Oral vaccines are likely to be solid which have proven to be more stable and less likely to freeze; this stability eliminates the need for a "cold chain": the resources required to keep vaccines within a restricted temperature range from the manufacturing stage to the point of administration, which, in turn, will decrease costs of vaccines. Finally, a microneedle approach, which is still in stages of development, seems to be the vaccine of the future, the microneedle, which is "pointed projections fabricated into arrays that can create vaccine delivery pathways through the skin".[19]

Plasmids

The use of plasmids has been validated in preclinical studies as a protective vaccine strategy for cancer and infectious diseases. However, the crossover application into human studies has been met with poor results based on the inability to provide clinically relevant benefit. The overall efficacy of plasmid DNA immunization depends on increasing the plasmid's immunogenicity while also correcting for factors involved in the specific activation of immune effector cells. [20]

Use in nonhumans

See also: Influenza vaccine § Flu vaccine for nonhumans, and Vaccination of dogs

Vaccinations of animals are used both to prevent their contracting diseases and to prevent transmission of disease to humans. Both animals kept as pets and animals raised as livestock are routinely vaccinated. In some instances, wild populations may be vaccinated. This is sometimes accomplished with vaccine-laced food spread in a disease-prone area and has been used to attempt to control rabies in raccoons.

Where rabies occurs, rabies vaccination of dogs may be required by law. Other canine vaccines include canine distemper, canine parvovirus, infectious canine hepatitis, adenovirus-2, leptospirosis, bordatella, canine parainfluenza virus, and Lyme disease among others.

Vaccine development has several trends:[21]

  • Until now, most vaccines have been aimed at infants and children, but adolescents and adults are increasingly being targeted.
  • Combinations of vaccines are becoming more common; vaccines containing five or more components are used in many parts of the world.
  • New methods of administering vaccines are being developed, such as skin patches, aerosols via inhalation devices, and eating genetically engineered plants.
  • Vaccines are being designed to stimulate innate immune responses, as well as adaptive.
  • Attempts are being made to develop vaccines to help cure chronic infections, as opposed to preventing disease.
  • Vaccines are being developed to defend against bioterrorist attacks such as anthrax, plague, and smallpox.

Principles that govern the immune response can now be used in tailor-made vaccines against many noninfectious human diseases, such as cancers and autoimmune disorders.[22] For example, the experimental vaccine CYT006-AngQb has been investigated as a possible treatment for high blood pressure.[23]

See also

References

  1. ^ The Main Types of Vaccines
  2. ^ "Monovalent" at Dorland's Medical Dictionary
  3. ^ Polyvalent vaccine at Dorlands Medical Dictionary
  4. ^ "Questions and answers on monovalent oral polio vaccine type 1 (mOPV1) "Issued jointly by WHO and UNICEF"".
  5. ^ Orenstein WA, Papania MJ, Wharton ME (2004). "Measles elimination in the United States". J. Infect. Dis. 189 Suppl 1: S1–3. PMID 15106120. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  6. ^ a b c "Measles--United States, January 1-April 25, 2008". MMWR Morb. Mortal. Wkly. Rep. 57 (18): 494–8. 2008. PMID 18463608. {{cite journal}}: Unknown parameter |month= ignored (help)
  7. ^ Invacc-system
  8. ^ a b Wolfe R, Sharp L (2002). "Anti-vaccinationists past and present". BMJ. 325 (7361): 430–2. doi:10.1136/bmj.325.7361.430. PMID 12193361.
  9. ^ Bonhoeffer J, Heininger U (2007). "Adverse events following immunization: perception and evidence". Curr Opin Infect Dis. 20 (3): 237–46. doi:10.1097/QCO.0b013e32811ebfb0. PMID 17471032.
  10. ^ a b Demicheli V, Jefferson T, Rivetti A, Price D (2005). "Vaccines for measles, mumps and rubella in children". Cochrane Database Syst Rev. 19 (4). doi:10.1002/14651858.CD004407.pub2. PMID 16235361. {{cite journal}}: Unknown parameter |laydate= ignored (help); Unknown parameter |laysource= ignored (help); Unknown parameter |laysummary= ignored (help)CS1 maint: multiple names: authors list (link)
  11. ^ a b Halvorsen R (2007). The Truth about Vaccines. Gibson Square. ISBN 9781903933923.
  12. ^ Sinal SH, Cabinum-Foeller E, Socolar R (2008). "Religion and medical neglect". South Med J. 101 (7): 703–6. doi:10.1097/SMJ.0b013e31817997c9. PMID 18580731. {{cite journal}}: Unknown parameter |doi_brokendate= ignored (|doi-broken-date= suggested) (help)CS1 maint: multiple names: authors list (link)
  13. ^ a b Goodman, Jesse L. (2005-05-04). "Statement of Jesse L. Goodman, M.D., M.P.H. Director, Center for Biologics, Evaluation and Research Before the Committee on Energy and Commerce United States House of Representatives". Retrieved 2008-06-15. {{cite news}}: Cite has empty unknown parameter: |coauthors= (help)
  14. ^ Hardman Reis T (2006). "The role of intellectual property in the global challenge for immunization". J World Intellect Prop. 9 (4): 413–25. doi:10.1111/j.1422-2213.2006.00284.x.
  15. ^ "Thimerosal in vaccines". Center for Biologics Evaluation and Research, U.S. Food and Drug Administration. 2007-09-06. Retrieved 2007-10-01.
  16. ^ Bigham M, Copes R (2005). "Thiomersal in vaccines: balancing the risk of adverse effects with the risk of vaccine-preventable disease". Drug Saf. 28 (2): 89–101. doi:10.2165/00002018-200528020-00001. PMID 15691220.
  17. ^ Offit PA (2007). "Thimerosal and vaccines—a cautionary tale". N Engl J Med. 357 (13): 1278–9. doi:10.1056/NEJMp078187. PMID 17898096.
  18. ^ Morein B, Hu KF, Abusugra I (2004). "Current status and potential application of ISCOMs in veterinary medicine". Adv Drug Deliv Rev. 56 (10): 1367–82. doi:10.1016/j.addr.2004.02.004. PMID 15191787.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  19. ^ Giudice EL, Campbell JD (2006). "Needle-free vaccine delivery". Adv Drug Deliv Rev. 58 (1): 68–89. doi:10.1016/j.addr.2005.12.003. PMID 16564111.
  20. ^ Lowe; et al. (2008). "Plasmid DNA as Prophylactic and Therapeutic vaccines for Cancer and Infectious Diseases". Plasmids: Current Research and Future Trends. Caister Academic Press. ISBN 978-1-904455-35-6. {{cite book}}: Explicit use of et al. in: |author= (help); External link in |chapterurl= (help); Unknown parameter |chapterurl= ignored (|chapter-url= suggested) (help)
  21. ^ Plotkin SA (2005). "Vaccines: past, present and future". Nat Med. 11 (4 Suppl): S5–11. doi:10.1038/nm1209. PMID 15812490.
  22. ^ Spohn G, Bachmann MF (2008). "Exploiting viral properties for the rational design of modern vaccines". Expert Rev Vaccines. 7 (1): 43–54. doi:10.1586/14760584.7.1.43. PMID 18251693.
  23. ^ Samuelsson O, Herlitz H (2008). "Vaccination against high blood pressure: a new strategy". Lancet. 371 (9615): 788–9. doi:10.1016/S0140-6736(08)60355-4. PMID 18328909.


Template:Link FA

Retrieved from "https://en.wikipedia.org/w/index.php?title=Vaccine&oldid=258431109"