|A glass of milk|
Milk allergy is an adverse immune reaction to one or more proteins in cow's milk. When allergy symptoms occur, those can be rapid or gradual in onset. The former may include anaphylaxis, a potentially life-threatening condition which requires treatment with epinephrine among other measures. The latter can take hours to days to appear, with symptoms including atopic dermatitis, inflammation of the esophagus, enteropathy involving the small intestine and proctocolitis involving the rectum and colon.
In the United States, 90% of allergic responses to foods are caused by eight foods, with cow's milk being the most common. Recognition that a small number of foods are responsible for the majority of food allergies has led to requirements to prominently list these common allergens, including dairy, on food labels. One function of the immune system is to defend against infections by recognizing foreign proteins. It should not over-react to food proteins. Stomach acids cause most proteins to become denatured, meaning to lose 3-dimensional configuration, and thus lose allergenicity. Heat via cooking can have the same effect. Immune tolerance is another safeguard to not over-reacting to food proteins.
Management is by avoiding eating any dairy foods or foods that contain dairy ingredients. In people with rapid reactions (IgE-mediated milk allergy) the dose capable of provoking an allergic response can be a few milligrams, so recommendations are to avoid dairy strictly. The declaration of the presence of trace amounts of milk or in foods is not mandatory in any country, with the exception of Brazil. Milk allergy affects between 2% and 3% of babies and young children. To reduce risk, recommendations are that babies should be exclusively breastfed for at least four months, preferably six months before introducing cow's milk. If there is a family history of dairy allergy then soy infant formula can be considered, but about 10 to 15% of babies allergic to cow's milk will also react to soy. The majority of children outgrow milk allergy, but for about 0.5% the condition persists into adulthood. Oral immunotherapy is being researched, but it is of unclear benefit.
- 1 Signs and symptoms
- 2 Mechanisms
- 3 Diagnosis
- 4 Prevention
- 5 Treatment
- 6 Prognosis
- 7 Epidemiology
- 8 Society and culture
- 9 Research
- 10 See also
- 11 References
- 12 External links
Signs and symptoms
Food allergies can have rapid onset (from minutes up to 2 hours), delayed onset (up to 48 hours or even 1 week), or combinations of both, depending on the mechanisms involved. The difference depends on the types of white blood cells involved. B cells, a subset of white blood cells, rapidly synthesize and secrete immunoglobulin E (IgE) a class of antibody which bind to antigens, i.e., the foreign proteins. Thus, immediate reactions are described as IgE-mediated. The delayed reactions involve non–IgE-mediated immune mechanisms initiated by B cells, T cells, and other white blood cells. Unlike with IgE reactions, there are no specific biomarker molecules circulating in the blood, and so, confirmation is by removing the suspect food from the diet and see if the symptoms resolve.
IgE mediated symptoms include: rash, hives, itching of mouth, lips, tongue, throat, eyes, skin, or other areas, swelling of lips, tongue, eyelids, or the whole face, difficulty swallowing, runny or congested nose, hoarse voice, wheezing, shortness of breath, diarrhea, abdominal pain, lightheadedness, fainting, nausea and vomiting. Symptoms of allergies vary from person to person and may vary from incident to incident. Serious danger regarding allergies can begin when the respiratory tract or blood circulation is affected. The former can be indicated by wheezing, a blocked airway and cyanosis, the latter by weak pulse, pale skin, and fainting. When these symptoms occur, the allergic reaction is called anaphylaxis. Anaphylaxis occurs when IgE antibodies are involved, and areas of the body that are not in direct contact with the food become affected and show severe symptoms. Untreated, this can proceed to vasodilation, a low blood pressure situation called anaphylactic shock, and death (very rare).
For milk allergy, non-IgE-mediated responses are more common than IgE-mediated. The presence of certain symptoms, such as angioedema or atopic eczema, is more likely related to IgE-mediated allergies, whereas non-IgE mediated reactions manifest as gastrointestinal symptoms, without cutaneous or respiratory symptoms. Within non-IgE cow's milk allergy, clinicians distinguish among food protein-induced enterocolitis syndrome (FPIES), food protein-induced allergic proctocolitis (FPIAP) and food protein-induced enteropathy (FPE). Common trigger foods for all are cow's milk and soy foods (including soy formula). FPIAP is considered to be at the milder end of the spectrum, and is characterized by intermittent bloody stools. FPE is identified by chronic diarrhea which will resolve when the offending food is removed from the infant's diet. FPIES can be severe, characterized by persistent vomiting 1–4 hours after an allergen-containing food, to the point of lethargy. Watery and sometimes bloody diarrhea can develop 5–10 hours after the triggering meal, to the point of dehydration and low blood pressure. Infants reacting to cow's milk may also react to soy formula, and vice versa. International consensus guidelines have been established for the diagnosis and treatment of FPIES.
Conditions caused by food allergies are classified into three groups according to the mechanism of the allergic response:
- IgE-mediated (classic) – the most common type, manifesting acute changes that occur shortly after eating, and may progress to anaphylaxis
- Non-IgE mediated – characterized by an immune response not involving immunoglobulin E; may occur hours to days after eating, complicating diagnosis
- IgE and non-IgE-mediated – a hybrid of the above two types
Allergic reactions are hyperactive responses of the immune system to generally innocuous substances, such as proteins in the foods we eat. Some proteins trigger allergic reactions while others do not. One theory is resistance to digestion, the thinking being that when largely intact proteins reach the small intestine the white blood cells involved in immune reactions will be activated. The heat of cooking structurally degrades protein molecules, potentially making them less allergenic. Allergic responses can be divided into two phases: an acute response that occurs immediately after exposure to an allergen, which can then either subside or progress into a "late-phase reaction," prolonging the symptoms of a response and resulting in more tissue damage.
In the early stages of acute allergic reaction, lymphocytes previously sensitized to a specific protein or protein fraction react by quickly producing a particular type of antibody known as secreted IgE (sIgE), which circulates in the blood and binds to IgE-specific receptors on the surface of other kinds of immune cells called mast cells and basophils. Both of these are involved in the acute inflammatory response. Activated mast cells and basophils undergo a process called degranulation, during which they release histamine and other inflammatory chemical mediators called (cytokines, interleukins, leukotrienes, and prostaglandins) into the surrounding tissue causing several systemic effects, such as vasodilation, mucous secretion, nerve stimulation, and smooth-muscle contraction. This results in runny nose, itchiness, shortness of breath, and potentially anaphylaxis. Depending on the individual, the allergen, and the mode of introduction, the symptoms can be system-wide (classical anaphylaxis), or localized to particular body systems; asthma is localized to the respiratory system while eczema is localized to the skin.
After the chemical mediators of the acute response subside, late-phase responses can often occur due to the migration of other white blood cells such as neutrophils, lymphocytes, eosinophils, and macrophages to the initial reaction sites. This is usually seen 2–24 hours after the original reaction. Cytokines from mast cells may also play a role in the persistence of long-term effects. Late-phase responses seen in asthma are slightly different from those seen in other allergic responses, although they are still caused by release of mediators from eosinophils.
Six major allergenic proteins from cow's milk have been identified: αs1-, αs2-, β-, and κ-casein from casein proteins and α-lactalbumin and β-lactoglobulin from whey proteins. There is some cross-reactivity with soy protein, particularly in non-IgE mediated allergy. Heat can reduce allergenic potential, so dairy ingredients in baked goods may be less likely to trigger a reaction than milk or cheese. For milk allergy, non-IgE-mediated responses are more common than IgE-mediated. The former can manifest as atopic dermatitis and gastrointestinal symptoms, especially in infants and young children. Some will display both, so that a child could react to an oral food challenge with respiratory symptoms and hives (skin rash), followed a day or two later with a flare up of atopic dermatitis and gastroinstestinal symptoms, including chronic diarrhea, blood in the stools, gastroesophageal reflux disease (GERD), constipation, chronic vomiting and colic.
Diagnosis of milk allergy is based on the person's history of allergic reactions, skin prick test (SPT), patch test, and measurement of milk protein specific serum immunoglobulin E. A negative IgE test does not rule out non-IgE mediated allergy, also described as cell-mediated allergy. Confirmation is by double-blind, placebo-controlled food challenges, conducted by an allergy specialist. SPT and IgE have sensitivity around 88% but specificity of 68% and 48%, respectively, meaning these tests will probably detect a milk sensitivity but will also be positive for other allergens.
Attempts have been made to identify SPT and IgE responses accurate enough to avoid the need for a confirming oral food challenge. A systematic review stated that for children younger than two years, cut-offs for specific IgE or SPT seem to be more homogeneous and may be proposed. For older children the tests were less consistent. It concluded "None of the cut-offs proposed in the literature can be used to definitely confirm cow's milk allergy diagnosis, either to fresh pasteurized or to baked milk."
The symptoms of milk allergy can be confused with other disorders that present similar clinical features, such as lactose intolerance, infectious gastroenteritis, celiac disease, non-celiac gluten sensitivity, inflammatory bowel disease, eosinophilic gastroenteritis, and pancreatic insufficiency, among others.
Milk allergy is distinct from lactose intolerance, which is a nonallergic food sensitivity, due to the lack of enzyme lactase in the small intestines to break lactose down into glucose and galactose. The unabsorbed lactose reaches the large intestine, where resident bacteria use it for fuel, releasing hydrogen, carbon dioxide and methane gases. These gases are the cause of abdominal pain and other symptoms. Lactose intolerance does not cause damage to the gastrointestinal tract. There are four types: primary, secondary, developmental, and congenital. Primary lactose intolerance is when the amount of lactase declines as people age. Secondary lactose intolerance is due to injury to the small intestine such as from infection, celiac disease, inflammatory bowel disease, or other diseases. Developmental lactose intolerance may occur in premature babies and usually improves over a short period of time. Congenital lactose intolerance is an extremely rare genetic disorder in which little or no lactase is made from birth.
Research on prevention addresses the question of whether it is possible to reduce the risk of developing an allergy in the first place. Two reviews concluded that there is no strong evidence to recommend changes to the diets of pregnant or nursing women as a means of preventing the development of food allergy in their infants. For mothers of infants considered at high risk of developing cow's milk allergy because of a family history, there is some evidence that the nursing mother avoiding allergens may reduce risk of the child developing eczema, but the Cochrane review concluded that more research is needed.
Guidelines from various government and international organizations recommend that for the lowest allergy risk, infants be exclusively breastfed for 4–6 months. There does not appear to be any benefit to extending that period beyond six months. If a nursing mother decides to start feeding with an infant formula prior to four months the recommendation is to use a formula containing cow's milk proteins.
A different consideration occurs when there is a family history - either parents or older siblings - of milk allergy. The three options to avoiding formula with intact cow's milk proteins are substituting a product containing either extensively hydrolyzed milk proteins, or a non-dairy formula, or one utilizing free amino acids. The hydrolyzing process breaks intact proteins into fragments, in theory reducing allergenic potential. In 2016 the U.S. Food and Drug Administration (FDA) approved a label claim for hydrolyzed whey protein being hypoallergenic. However, a meta-analysis published the same year disputed this claim, concluding that based on dozens of clinical trials there was insuficient evidence to support a claim that a partially hydrolyzed formula could reduce the risk of eczema. Soy formula is a common substitution, but infants with milk allergy may have an allergic response to soy formula. Hydrolyzed rice formula is an option, as are the more expensive amino acid-based formulas.
The need for a dairy-free diet should be reevaluated every six months by testing milk-containing products low on the "milk ladder", such as fully cooked, i.e., baked foods, containing milk, in which the milk proteins have been denatured, and ending with fresh cheese and milk. Desensitization via oral immunotherapy is considered experimental.
Treatment for accidental ingestion of milk products by allergic individuals varies depending on the sensitivity of the person. An antihistamine such as diphenhydramine (Benadryl) may be prescribed. Sometimes prednisone will be prescribed to prevent a possible late phase Type I hypersensitivity reaction. Severe allergic reactions (anaphylaxis) may require treatment with an epinephrine pen, i.e., an injection device designed to be used by a non-healthcare professional when emergency treatment is warranted. A second dose is needed in 16–35% of episodes.
Most people find it necessary to strictly avoid any item containing dairy ingredients. The reason is that the individual threshold dose capable of provoking an allergic reaction can be quite small, especially in infants. An estimated 5% react to less than 30 milligrams of dairy proteins, and 1% react to less than 1 milligram. A more recent review calculated that the eliciting threshold dose for an allergic reaction in 1% of people (ED01) with confirmed cow's milk allergy is 0.1 mg of cow's milk protein.
Beyond the obvious (anything with milk, cheese, cream, curd, butter, ghee or yogurt in the name), in countries where allergen labeling is mandatory, the ingredient list is supposed to list all ingredients. Anyone with or caring for a person with a dairy protein allergy should always carefully read food package labels, as sometimes even a familiar brand undergoes an ingredient change. In the United States, for all foods except meat, poultry and egg processed products and most alcoholic beverages, if an ingredient is derived from one of the required-label allergens, then it must either have the food name in parentheses, for example "Casein (milk)," or as an alternative, there must be a statement separate but adjacent to the ingredients list: "Contains milk" (and any other of the allergens with mandatory labeling). Diary-sourced protein ingredients include casein, caseinates, whey and lactalbumin, among others. The U.S. FDA has a recall process for foods that contain undeclared allergenic ingredients. The University of Wisconsin has a list of foods that may contain dairy proteins, yet are not always obvious from the name or type of food. This list contains the following examples:
- Bread, baked goods and desserts
- Caramel and nougat candies
- Cereals, crackers, food bars
- Chewing gum
- Chocolate ('milk' and 'dark')
- "Cream of..." soups
- Creamy pasta sauces
- Creamy salad dressings
- Flavored potato chips
- Hot dogs and lunch meat
- Instant mashed potatoes
- Medical food beverages
- Non-dairy creamer
- Pudding and custard
There is a distinction between “Contains ___” and “May contain ___.” The first is a deliberate addition to the ingredients of a food, and is required. The second addresses unintentional possible inclusion of ingredients, in this instance dairy-sourced, during transportation, storage or at the manufacturing site, and is voluntary, and is referred to as precautionary allergen labeling (PAL). (for more information see regulation of labelling)
Milk from other species (goat, sheep...) should not be used as a substitute for cow's milk, as milk proteins from other mammals are often cross-reactive. Nevertheless, some people with cow's milk allergy can tolerate goat’s or sheep’s milk, and vice versa. Milk from camels, pigs, reindeer, horses, and donkeys may also be tolerated in some cases. Probiotic products have been tested, and some found to contain milk proteins which were not always indicated on the labels.
Cross-reactivity with soy
Infants - either still 100% breastfeeding or on infant formula - and also young children - may be prone to a combined cow's milk and soy protein allergy referred to as "milk soy protein intolerance" (MSPI). A U.S. state government website presents the concept, including a recommendation that nursing mothers discontinue eating any foods that contain dairy or soy ingredients. In opposition to this recommendation, a published scientific review stated that there was not yet sufficient evidence in the human trial literature to conclude that maternal dietary food avoidance during lactation would prevent or treat allergic symptoms in breastfed infants.
A review presented information on milk allergy, soy allergy and cross reactivity between the two. Milk allergy was described as occurring in 2.2% to 2.8% of infants and declining with age. Soy allergy was described as occurring in zero to 0.7% of young children. According to several studies cited in the review, between 10% and 14% of infants and young children with confirmed cow's milk allergy were determined to also be sensitized to soy and in some instances have a clinical reaction after consuming a soy-containing food. The research did not address whether the cause was two separate allergies or a cross-reaction due to a similarity in protein structure, as which occurs for cow's milk and goat's milk. Recommendations are that infants diagnosed as allergic to cow's milk infant formula be switched to an extensively hydrolyzed protein formula rather than a soy whole protein formula.
Milk allergy typically presents in the first year of life. The majority of children outgrow milk allergy by the age of ten years. One large clinical trial reported resolutions of 19% by age 4 years, 42% by age 8 years, 64% by age 12 years, and 79% by 16 years. Children are often better able to tolerate milk as an ingredient in baked goods relative to liquid milk. Childhood predictors for adult-persistence are anaphylaxis, high milk-specific serum immunoglobulin E (IgE), robust response to the skin prick test and absence of tolerance to milk-containing baked foods. Resolution was more likely if baseline serum IgE was lower, or if IgE-mediated allergy was absent so that all that was present was cell-mediated, non-IgE allergy. People with confirmed cow's milk allergy may also demonstrate an allergic response to beef, more so to rare beef versus well-cooked beef. The offending protein appears to be bovine serum albumin.
Milk allergy has consequences. In a U.S. government diet and health surveys conducted in 2007-2010, 6,189 children ages 2-17 years were assessed. For those classified as cow's milk allergic at the time of the survey, mean weight, height and body-mass index were significantly lower than their non-allergic peers. This was not true for children with other food allergies. Diet assessment showed a significant 23% reduction of calcium intake and near-significant trends for lower vitamin D and total calorie intake.
The percentage of babies in developed countries with milk allergy is between 2% and 3%. This estimate is for antibody-based allergy; figures for allergy based on cellular immunity are unknown. The percentage declines as children get older. National survey data in the United States collected 2005–2006 showed that from age six and older, the percentage with IgE-confirmed milk allergy was under 0.4%. For all age groups, a review conducted in Europe estimated 0.6% had milk allergy.
Society and culture
With the passage of mandatory labeling laws, food allergy awareness has definitely increased, with impacts on the quality of life for children, their parents and their immediate caregivers. In the United States, the Food Allergen Labeling and Consumer Protection Act of 2004 causes people to be reminded of allergy problems every time they handle a food package, and restaurants have added allergen warnings to menus. The Culinary Institute of America, a premier school for chef training, has courses in allergen-free cooking and a separate teaching kitchen. School systems have protocols about what foods can be brought into the school. Despite all these precautions, people with serious allergies are aware that accidental exposure can easily occur at other peoples' houses, at school or in restaurants. Food fear has a significant impact on quality of life. Finally, for children with allergies, their quality of life is also affected by actions of their peers. There is an increased occurrence of bullying, which can include threats or acts of deliberately being touched with foods they need to avoid, also having their allergen-free food deliberately contaminated.
Regulation of labeling
In response to the risk that certain foods pose to those with food allergies, some countries have responded by instituting labeling laws that require food products to clearly inform consumers if their products contain major allergens or byproducts of major allergens among the ingredients intentionally added to foods. Nevertheless, there are no labeling laws to mandatory declare the presence of trace amounts in the final product as a consequence of cross-contamination, except in Brazil.
Ingredients intentionally added
In the United States, the Food Allergen Labeling and Consumer Protection Act of 2004 (FALCPA) requires companies to disclose on the label whether a packaged food product contains a major food allergen added intentionally: cow's milk, peanuts, eggs, shellfish, fish, tree nuts, soy and wheat. This list originated in 1999 from the World Health Organisation Codex Alimentarius Commission. To meet FALCPA labeling requirements, if an ingredient is derived from one of the required-label allergens, then it must either have its "food sourced name" in parentheses, for example "Casein (milk)," or as an alternative, there must be a statement separate but adjacent to the ingredients list: "Contains milk" (and any other of the allergens with mandatory labeling). Dairy food listing is also mandatory in the European Union and more than a dozen other countries.
FALCPA applies to packaged foods regulated by the FDA, which does not include poultry, most meats, certain egg products, and most alcoholic beverages. However, some meat, poultry, and egg processed products may contain allergenic ingredients, such as added milk proteins. These products are regulated by the Food Safety and Inspection Service (FSIS), which requires that any ingredient be declared in the labeling only by its common or usual name. Neither the identification of the source of a specific ingredient in a parenthetical statement nor the use of statements to alert for the presence of specific ingredients, like "Contains: milk", are mandatory according to FSIS.
In the United States, there is no federal mandate to address the presence of allergens in drug products. FALCPA does not apply to medicines nor to cosmetics. FALCPA also does not apply to food prepared in restaurants.
Trace amounts as a result of cross-contamination
The value of allergen labeling other than for intentional ingredients is controversial. This concerns labeling for ingredients present unintentionally as a consequence of cross-contact or cross-contamination at any point along the food chain (during raw material transportation, storage or handling, due to shared equipment for processing and packaging, etc.). Experts in this field propose that if allergen labeling is to be useful to consumers, and healthcare professionals who advise and treat those consumers, ideally there should be agreement on which foods require labeling, threshold quantities below which labeling may be of no purpose, and validation of allergen detection methods to test and potentially recall foods that were deliberately or inadvertently contaminated.
Labeling regulations have been modified to provide for mandatory labeling of ingredients plus voluntary labeling, termed precautionary allergen labeling (PAL), also known as "may contain" statements, for possible, inadvertent, trace amount, cross-contamination during production. PAL labeling can be confusing to consumers, especially as there can be many variations on the wording of the warning. As of 2014[update] PAL is regulated only in Switzerland, Japan, Argentina, and South Africa. Argentina decided to prohibit precautionary allergen labeling since 2010, and instead puts the onus on the manufacturer to control the manufacturing process and label only those allergenic ingredients known to be in the products. South Africa does not permit the use of PAL, except when manufacturers demonstrate the potential presence of allergen due to cross-contamination through a documented risk assessment and despite adherence to Good Manufacturing Practice. In Australia and New Zealand there is a recommendation that PAL be replaced by guidance from VITAL 2.0 (Vital Incidental Trace Allergen Labeling). A review identified "the eliciting dose for an allergic reaction in 1% of the population" as 0.01 mg for cow's milk. This threshold reference dose (and similar results for egg, peanut and other proteins) will provide food manufacturers with guidance for developing precautionary labeling and give consumers a better idea of might be accidentally in a food product beyond "may contain." VITAL 2.0 was developed by the Allergen Bureau, a food industry sponsored, non-government organization. The European Union has initiated a process to create labeling regulations for unintentional contamination but is not expected to publish such before 2024.
Lack of compliance with labeling regulations is also a problem. As an example, the FDA documented failure to list milk as an ingredient in dark chocolate bars. The FDA tested 94 dark chocolate bars for the presence of milk. Only six listed milk as an ingredient, but of the remaining 88, the FDA found that 51 of them actually did contain milk proteins. Many of those did have PAL wording such as "may contain dairy." Others claimed to be "dairy free" or "vegan" but still tested positive for cow's milk proteins.
In Brazil since April 2016, the declaration of the possibility of cross-contamination is mandatory when the product does not intentionally add any allergenic food or its derivatives, but the Good Manufacturing Practices and allergen control measures adopted are not sufficient to prevent the presence of accidental trace amounts. Milk of all species of mammalians is included among these allergenic foods.
Desensitization, which is a slow process of eating tiny amounts of the allergenic protein, until the body is able to tolerate more significant exposure, results in reduced symptoms or even remission of the allergy in some people and is being explored for milk allergy. This is called oral immunotherapy (OIT). Sublingual immunotherapy, in which the allergenic protein is held in the mouth, under the tongue, has been approved for grass and ragweed allergies, but not yet for foods. Oral desensitization for cow's milk allergy appears to be relatively safe and may be effective, however further studies are required to understand the overall immune response, and questions remain open about duration of the desensitization.
There is research - not specific to milk allergy - on probiotics, prebiotics and the combination of the two (synbiotics) as a means of treating or preventing infant and child allergies. From reviews, there appears to be a treatment benefit for eczema, but not asthma, wheezing or rhinoconjunctivitis. Several reviews concluded that the evidence cannot yet be recommended for clinical practice.
- List of allergens (food and non-food)
- Nwaru BI, Hickstein L, Panesar SS, Roberts G, Muraro A, Sheikh A (2014). "Prevalence of common food allergies in Europe: a systematic review and meta-analysis". Allergy. 69 (8): 992–1007. doi:10.1111/all.12423. PMID 24816523.
- Caffarelli, Carlo; Baldi, Francesco; Bendandi, Barbara; Calzone, Luigi; Marani, Miris; Pasquinelli, Pamela; Ewgpag, On Behalf of (2010). "Cow's milk protein allergy in children: A practical guide". Italian Journal of Pediatrics. 36: 5. doi:10.1186/1824-7288-36-5. PMC . PMID 20205781.
- "Asthma and Allergy Foundation of America". Archived from the original on 6 October 2012. Retrieved 23 December 2012.
- FDA. "Food Allergen Labeling and Consumer Protection Act of 2004 Questions and Answers". Retrieved 29 September 2017.
- FDA (18 December 2017). "Food Allergies: What You Need to Know". Retrieved 12 January 2018.
- Urisu A, Ebisawa M, Ito K, Aihara Y, Ito S, Mayumi M, Kohno Y, Kondo N (2014). "Japanese Guideline for Food Allergy 2014". Allergol Int. 63 (3): 399–419. doi:10.2332/allergolint.14-RAI-0770. PMID 25178179.
- "Food allergen labelling and information requirements under the EU Food Information for Consumers Regulation No. 1169/2011: Technical Guidance" (April 2015).
- Lifschitz C, Szajewska H (Feb 2015). "Cow's milk allergy: evidence-based diagnosis and management for the practitioner". Eur J Pediatr. 174 (2): 141–150. doi:10.1007/s00431-014-2422-3. PMC . PMID 25257836.
- Taylor SL, Hefle SL (2006). "Food allergen labeling in the USA and Europe". Curr Opin Allergy Clin Immunol (Review). 6 (3): 186–190. doi:10.1097/01.all.0000225158.75521.ad. PMID 16670512.
- Taylor SL, Hefle SL, Bindslev-Jensen C, Atkins FM, Andre C, Bruijnzeel-Koomen C, et al. (2004). "A consensus protocol for the determination of the threshold doses for allergenic foods: how much is too much?". Clin Exp Allergy (Review. Consensus Development Conference. Research Support, Non-U.S. Gov't). 34 (5): 689–695. doi:10.1111/j.1365-2222.2004.1886.x. PMID 15144458.
- Allen KJ, Turner PJ, Pawankar R, Taylor S, Sicherer S, Lack G, Rosario N, Ebisawa M, Wong G, Mills EN, Beyer K, Fiocchi A, Sampson HA (2014). "Precautionary labelling of foods for allergen content: are we ready for a global framework?". World Allergy Organ J. 7 (1): 10. doi:10.1186/1939-4551-7-10. PMC . PMID 24791183.
- "Agência Nacional de Vigilância Sanitária Guia sobre Programa de Controle de Alergênicos". Agência Nacional de Vigilância Sanitária (ANVISA). 2016. Retrieved 7 April 2018.
- Savage J, Johns CB (2015). "Food allergy: epidemiology and natural history". Immunol Allergy Clin North Am. 35 (1): 45–59. doi:10.1016/j.iac.2014.09.004. PMC . PMID 25459576.
- Vandenplas Y (2017). "Prevention and Management of Cow's Milk Allergy in Non-Exclusively Breastfed Infants". Nutrients. 9 (7): 731. doi:10.3390/nu9070731. PMC . PMID 28698533.
- Martorell Calatayud C, Muriel García A, Martorell Aragonés A, De La Hoz Caballer B (2014). "Safety and efficacy profile and immunological changes associated with oral immunotherapy for IgE-mediated cow's milk allergy in children: systematic review and meta-analysis". J Investig Allergol Clin Immunol. 24 (5): 298–307. PMID 25345300.
- Brożek JL, Terracciano L, Hsu J, Kreis J, Compalati E, Santesso N, Fiocchi A, Schünemann HJ (2012). "Oral immunotherapy for IgE-mediated cow's milk allergy: a systematic review and meta-analysis". Clin. Exp. Allergy. 42 (3): 363–374. doi:10.1111/j.1365-2222.2011.03948.x. PMID 22356141.
- Koletzko S, Niggemann B, Arato A, Dias JA, Heuschkel R, Husby S; et al. (2012). "Diagnostic approach and management of cow's-milk protein allergy in infants and children: ESPGHAN GI Committee practical guidelines". J Pediatr Gastroenterol Nutr (Practice Guideline). 55 (2): 221–229. doi:10.1097/MPG.0b013e31825c9482. PMID 22569527.
- MedlinePlus Encyclopedia Food allergy
- Sicherer SH, Sampson HA (2014). "Food allergy: Epidemiology, pathogenesis, diagnosis, and treatment". J Allergy Clin Immunol. 133 (2): 291–307. doi:10.1016/j.jaci.2013.11.020. PMID 24388012.
- Venter, Carina; Brown, Trevor; Meyer, Rosan; Walsh, Joanne; Shah, Neil; Nowak-Węgrzyn, Anna; Chen, Tong-Xin; Fleischer, David M; Heine, Ralf G; Levin, Michael; Vieira, Mario C; Fox, Adam T (2017). "Better recognition, diagnosis and management of non-IgE-mediated cow's milk allergy in infancy: IMAP—an international interpretation of the MAP (Milk Allergy in Primary Care) guideline". Clinical and Translational Allergy. 7: 26. doi:10.1186/s13601-017-0162-y. PMC . PMID 28852472.
- Leonard, Stephanie A (2017). "Non-IgE-mediated Adverse Food Reactions". Current Allergy and Asthma Reports. 17 (12): 84. doi:10.1007/s11882-017-0744-8. PMID 29138990.
- Caubet JC, Szajewska H, Shamir R, Nowak-Węgrzyn A (2017). "Non-IgE-mediated gastrointestinal food allergies in children". Pediatr Allergy Immunol. 28 (1): 6–17. doi:10.1111/pai.12659. PMID 27637372.
- Nowak-Węgrzyn A, Chehade M, et al. (2017). "International consensus guidelines for the diagnosis and management of food protein-induced enterocolitis syndrome: Executive summary-Workgroup Report of the Adverse Reactions to Foods Committee, American Academy of Allergy, Asthma & Immunology". J. Allergy Clin. Immunol. 139 (4): 1111–1126.e4. doi:10.1016/j.jaci.2016.12.966. PMID 28167094.
- "Food allergy". NHS Choices. 16 May 2016. Retrieved 31 January 2017.
A food allergy is when the body's immune system reacts unusually to specific foods
- Food Reactions. Allergies Archived 2010-04-16 at the Wayback Machine.. Foodreactions.org. Kent, England. 2005. Accessed 27 Apr 2010.
- Mayo Clinic. Causes of Food Allergies. Archived 2010-02-27 at the Wayback Machine. April 2010.
- Janeway, Charles; Paul Travers; Mark Walport; Mark Shlomchik (2001). Immunobiology; Fifth Edition. New York and London: Garland Science. pp. e–book. ISBN 0-8153-4101-6. Archived from the original on 2009-06-28.
- Grimbaldeston MA, Metz M, Yu M, Tsai M, Galli SJ (2006). "Effector and potential immunoregulatory roles of mast cells in IgE-associated acquired immune responses". Curr. Opin. Immunol. 18 (6): 751–760. doi:10.1016/j.coi.2006.09.011. PMID 17011762.
- Holt PG, Sly PD (2007). "Th2 cytokines in the asthma late-phase response". Lancet. 370 (9596): 1396–1398. doi:10.1016/S0140-6736(07)61587-6. PMID 17950849.
- Soares-Weiser K, Takwoingi Y, Panesar SS, Muraro A, Werfel T, Hoffmann-Sommergruber K, Roberts G, Halken S, Poulsen L, van Ree R, Vlieg-Boerstra BJ, Sheikh A (2014). "The diagnosis of food allergy: a systematic review and meta-analysis". Allergy. 69 (1): 76–86. doi:10.1111/all.12333. PMID 24329961.
- Cuomo B, Indirli GC, Bianchi A, Arasi S, Caimmi D, Dondi A, La Grutta S, Panetta V, Verga MC, Calvani M (2017). "Specific IgE and skin prick tests to diagnose allergy to fresh and baked cow's milk according to age: a systematic review". Ital J Pediatr. 43 (1): 93. doi:10.1186/s13052-017-0410-8. PMC . PMID 29025431.
- Heine, Ralf G; Alrefaee, Fawaz; Bachina, Prashant; De Leon, Julie C; Geng, Lanlan; Gong, Sitang; Madrazo, José Armando; Ngamphaiboon, Jarungchit; Ong, Christina; Rogacion, Jossie M (2017). "Lactose intolerance and gastrointestinal cow's milk allergy in infants and children – common misconceptions revisited". World Allergy Organization Journal. 10 (1): 41. doi:10.1186/s40413-017-0173-0. PMC . PMID 29270244.
- Feuille, Elizabeth; Nowak-Węgrzyn, Anna (2015). "Food Protein-Induced Enterocolitis Syndrome, Allergic Proctocolitis, and Enteropathy". Current Allergy and Asthma Reports. 15 (8): 50. doi:10.1007/s11882-015-0546-9. PMID 26174434.
- Guandalini S, Newland C (2011). "Differentiating food allergies from food intolerances". Curr Gastroenterol Rep (Review). 13 (5): 426–434. doi:10.1007/s11894-011-0215-7. PMID 21792544.
- Deng Y, Misselwitz B, Dai N, Fox M (2015). "Lactose Intolerance in Adults: Biological Mechanism and Dietary Management". Nutrients (Review). 7 (9): 8020–8035. doi:10.3390/nu7095380. PMC . PMID 26393648.
- Heyman, M. B (2006). "Lactose Intolerance in Infants, Children, and Adolescents". Pediatrics. 118 (3): 1279–86. doi:10.1542/peds.2006-1721. PMID 16951027.
- "Lactose Intolerance". NIDDK. June 2014. Archived from the original on 25 October 2016. Retrieved 25 October 2016.
- Berni Canani, Roberto; Pezzella, Vincenza; Amoroso, Antonio; Cozzolino, Tommaso; Di Scala, Carmen; Passariello, Annalisa (2016). "Diagnosing and Treating Intolerance to Carbohydrates in Children". Nutrients. 8 (3): 157. doi:10.3390/nu8030157. PMC . PMID 26978392.
- de Silva D, Geromi M, Halken S, Host A, Panesar SS, Muraro A, Werfel T, Hoffmann-Sommergruber K, Roberts G, Cardona V, Dubois AE, Poulsen LK, Van Ree R, Vlieg-Boerstra B, Agache I, Grimshaw K, O'Mahony L, Venter C, Arshad SH, Sheikh A (2014). "Primary prevention of food allergy in children and adults: systematic review". Allergy. 69 (5): 581–589. doi:10.1111/all.12334. PMC . PMID 24433563.
- Kramer MS, Kakuma R (2014). "Maternal dietary antigen avoidance during pregnancy or lactation, or both, for preventing or treating atopic disease in the child". Evid Based Child Health. 9 (2): 447–483. doi:10.1002/ebch.1972. PMID 25404609.
- Anderson J, Malley K, Snell R (2009). "Is 6 months still the best for exclusive breastfeeding and introduction of solids? A literature review with consideration to the risk of the development of allergies". Breastfeed Rev. 17 (2): 23–31. PMID 19685855.
- Fiocchi A, Dahda L, Dupont C, Campoy C, Fierro V, Nieto A (2016). "Cow's milk allergy: towards an update of DRACMA guidelines". World Allergy Organ J. 9 (1): 35. doi:10.1186/s40413-016-0125-0. PMC . PMID 27895813.
- Labeling of Infant Formula: Guidance for Industry U.S. Food and Drug Administration (2016) Accessed 11 December 2017.
- Boyle RJ, Ierodiakonou D, Khan T, Chivinge J, Robinson Z, Geoghegan N, Jarrold K, Afxentiou T, Reeves T, Cunha S, Trivella M, Garcia-Larsen V, Leonardi-Bee J (2016). "Hydrolysed formula and risk of allergic or autoimmune disease: systematic review and meta-analysis". BMJ. 352: i974. doi:10.1136/bmj.i974. PMC . PMID 26956579.
- Kattan JD, Cocco RR, Järvinen KM (2011). "Milk and soy allergy". Pediatr Clin North Am (Review). 58 (2): 407–426, x. doi:10.1016/j.pcl.2011.02.005. PMC . PMID 21453810.
- Yeung, Joanne P.; Kloda, Lorie A.; McDevitt, Jason; Ben-Shoshan, Moshe; Alizadehfar, Reza (2012-11-14). "Oral immunotherapy for milk allergy". The Cochrane Database of Systematic Reviews. 11: CD009542. doi:10.1002/14651858.CD009542.pub2. PMID 23152278.
- Tang AW (2003). "A practical guide to anaphylaxis". Am Fam Physician. 68 (7): 1325–1332. PMID 14567487.
- The EAACI Food Allergy and Anaphylaxis Guidelines Group (August 2014). "Anaphylaxis: guidelines from the European Academy of Allergy and Clinical Immunology". Allergy. 69 (8): 1026–1045. doi:10.1111/all.12437. PMID 24909803.
- Moneret-Vautrin DA, Kanny G (2004). "Update on threshold doses of food allergens: implications for patients and the food industry". Curr Opin Allergy Clin Immunol (Review). 4 (3): 215–219. doi:10.1097/00130832-200406000-00014. PMID 15126945.
- Allen KJ, Remington BC, Baumert JL, Crevel RW, Houben GF, Brooke-Taylor S, Kruizinga AG, Taylor SL (2014). "Allergen reference doses for precautionary labeling (VITAL 2.0): clinical implications". J. Allergy Clin. Immunol. 133 (1): 156–164. doi:10.1016/j.jaci.2013.06.042. PMID 23987796.
- FDA (14 December 2017). "Have Food Allergies? Read the Label". Retrieved 14 January 2018.
- "Food Ingredients of Public Health Concern" (PDF). United States Department of Agriculture. Food Safety and Inspection Service. 7 March 2017. Retrieved 16 February 2018.
- "Allergies and Food Safety". United States Department of Agriculture. Food Safety and Inspection Service. 1 December 2016. Retrieved 16 February 2018.
- "Milk Allergy Diet" (PDF). University of Wisconsin Hospital and Clinics. Clinical Nutrition Services Department and the Department of Nursing. 2015. Retrieved 14 January 2018.
- FDA (12 October 2014). "Finding Food Allergens Where They Shouldn't Be". Retrieved 11 February 2018.
- Martorell-Aragonés A, Echeverría-Zudaire L, Alonso-Lebrero E, Boné-Calvo J, Martín-Muñoz MF, Nevot-Falcó S, et al. (2015). "Position document: IgE-mediated cow's milk allergy". Allergol Immunopathol (Madr) (Practice Guideline. Review). 43 (5): 507–526. doi:10.1016/j.aller.2015.01.003. PMID 25800671.
- Nanagas, Vivian C; Baldwin, James L; Karamched, Keerthi R (2017). "Hidden Causes of Anaphylaxis". Current Allergy and Asthma Reports. 17 (7): 44. doi:10.1007/s11882-017-0713-2. PMID 28577270.
- Martín-Muñoz MF, Fortuni M, Caminoa M, Belver T, Quirce S, Caballero T (2012). "Anaphylactic reaction to probiotics. Cow's milk and hen's egg allergens in probiotic compounds". Pediatr Allergy Immunol. 23 (8): 778–784. doi:10.1111/j.1399-3038.2012.01338.x. PMID 22957765.
- "Milk Soy Protein Intolerance (MSPI)". dhhs.ne.gov. 2017. Retrieved 14 February 2018.
- Kramer MS, Kakuma R (2014). "Maternal dietary antigen avoidance during pregnancy or lactation, or both, for preventing or treating atopic disease in the child". Evid Based Child Health. 9 (2): 447–483. doi:10.1002/ebch.1972. PMID 25404609.
- Bhatia J, Greer F (2008). "Use of soy protein-based formulas in infant feeding". Pediatrics. 121 (5): 1062–1068. doi:10.1542/peds.2008-0564. PMID 18450914.
- Skripak JM, Matsui EC, Mudd K, Wood RA (2007). "The natural history of IgE-mediated cow's milk allergy". J. Allergy Clin. Immunol. 120 (5): 1172–1177. doi:10.1016/j.jaci.2007.08.023. PMID 17935766.
- Fiocchi A, Restani P, Riva E (2000). "Beef allergy in children". Nutrition. 16 (6): 454–457. doi:10.1016/s0899-9007(00)00285-9. PMID 10869903.
- Robbins KA, Wood RA, Keet CA (2014). "Milk allergy is associated with decreased growth in US children". J. Allergy Clin. Immunol. 134 (6): 1466–1468.e6. doi:10.1016/j.jaci.2014.08.037. PMC . PMID 25312758.
- Liu AH, Jaramillo R, Sicherer SH, Wood RA, Bock SA, Burks AW, Massing M, Cohn RD, Zeldin DC (2010). "National prevalence and risk factors for food allergy and relationship to asthma: results from the National Health and Nutrition Examination Survey 2005–2006". J. Allergy Clin. Immunol. 126 (4): 798–806.e13. doi:10.1016/j.jaci.2010.07.026. PMC . PMID 20920770.
- Ravid NL, Annunziato RA, Ambrose MA, Chuang K, Mullarkey C, Sicherer SH, Shemesh E, Cox AL (2015). "Mental health and quality-of-life concerns related to the burden of food allergy". Psychiatr. Clin. North Am. 38 (1): 77–89. doi:10.1016/j.psc.2014.11.004. PMID 25725570.
- Morou Z, Tatsioni A, Dimoliatis ID, Papadopoulos NG (2014). "Health-related quality of life in children with food allergy and their parents: a systematic review of the literature". J Investig Allergol Clin Immunol. 24 (6): 382–395. PMID 25668890.
- Lange L (2014). "Quality of life in the setting of anaphylaxis and food allergy". Allergo J Int. 23 (7): 252–260. doi:10.1007/s40629-014-0029-x. PMC . PMID 26120535.
- van der Velde JL, Dubois AE, Flokstra-de Blok BM (2013). "Food allergy and quality of life: what have we learned?". Curr Allergy Asthma Rep. 13 (6): 651–661. doi:10.1007/s11882-013-0391-7. PMID 24122150.
- Culinary Institute of America Allergen-free dining oasis comes to the CIA (accessed 1 November 2017)
- Shah E, Pongracic J (2008). "Food-induced anaphylaxis: who, what, why, and where?". Pediatr Ann. 37 (8): 536–541. PMID 18751571.
- Fong AT, Katelaris CH, Wainstein B (2017). "Bullying and quality of life in children and adolescents with food allergy". J Paediatr Child Health. 53 (7): 630–635. doi:10.1111/jpc.13570. PMID 28608485.
- Shah AV, Serajuddin AT, Mangione RA (2017). "Making All Medications Gluten Free". J Pharm Sci. 107 (5): 1263–1268. doi:10.1016/j.xphs.2017.12.021. PMID 29287928.
- Roses JB (2011). "Food allergen law and the Food Allergen Labeling and Consumer Protection Act of 2004: falling short of true protection for food allergy sufferers". Food Drug Law J. 66 (2): 225–42, ii. PMID 24505841.
- FDA (18 July 2006). "Food Allergen Labeling And Consumer Protection Act of 2004 Questions and Answers". Retrieved 12 March 2018.
- Mills EN, Valovirta E, Madsen C, Taylor SL, Vieths S, Anklam E, Baumgartner S, Koch P, Crevel RW, Frewer L (2004). "Information provision for allergic consumers—where are we going with food allergen labelling?". Allergy. 59 (12): 1262–1268. doi:10.1111/j.1398-9995.2004.00720.x. PMID 15507093.
- Taylor, S. L; Baumert, J. L (2015). "Worldwide food allergy labeling and detection of allergens in processed foods". Chemical immunology and allergy. 101: 227–34. doi:10.1159/000373910 (inactive 2018-06-12). PMID 26022883.
- DunnGalvin A, Chan CH, et al. (2015). "Precautionary allergen labelling: perspectives from key stakeholder groups". Allergy. 70 (9): 1039–1051. doi:10.1111/all.12614. PMID 25808296.
- Zurzolo GA, de Courten M, Koplin J, Mathai ML, Allen KJ (2016). "Is advising food allergic patients to avoid food with precautionary allergen labelling out of date?". Curr Opin Allergy Clin Immunol. 16 (3): 272–277. doi:10.1097/ACI.0000000000000262. PMID 26981748.
- Taylor SL, Baumert JL, Kruizinga AG, Remington BC, Crevel RW, Brooke-Taylor S, Allen KJ, Houben G (2014). "Establishment of Reference Doses for residues of allergenic foods: report of the VITAL Expert Panel". Food Chem. Toxicol. 63: 9–17. doi:10.1016/j.fct.2013.10.032. PMID 24184597.
- The VITAL Program Allergen Bureau, Australia and New Zealand.
- Popping B, Diaz-Amigo C (2018). "European Regulations for Labeling Requirements for Food Allergens and Substances Causing Intolerances: History and Future". J AOAC Int. 101 (1): 2–7. doi:10.5740/jaoacint.17-0381. PMID 29202901.
- "Consumer Updates – Dark Chocolate and Milk Allergies". FDA. 2017. Retrieved 14 February 2018.
- Nowak-Węgrzyn A, Sampson HA (March 2011). "Future therapies for food allergies". J. Allergy Clin. Immunol. 127 (3): 558–573. doi:10.1016/j.jaci.2010.12.1098. PMC . PMID 21277625.
- Narisety SD, Keet CA (October 2012). "Sublingual vs oral immunotherapy for food allergy: identifying the right approach". Drugs. 72 (15): 1977–1989. doi:10.2165/11640800-000000000-00000. PMC . PMID 23009174.
- http://acaai.org/allergies/allergy-treatment/allergy-immunotherapy/sublingual-immunotherapy-slit/ Sublingual Therapy (SLIT) American College of Allergy, Asthma and Immunology
- Chang YS, Trivedi MK, Jha A, Lin YF, Dimaano L, García-Romero MT (2016). "Synbiotics for Prevention and Treatment of Atopic Dermatitis: A Meta-analysis of Randomized Clinical Trials". JAMA Pediatr. 170 (3): 236–242. doi:10.1001/jamapediatrics.2015.3943. PMID 26810481.
- Cuello-Garcia CA, Brożek JL, Fiocchi A, Pawankar R, Yepes-Nuñez JJ, Terracciano L, Gandhi S, Agarwal A, Zhang Y, Schünemann HJ (2015). "Probiotics for the prevention of allergy: A systematic review and meta-analysis of randomized controlled trials". J. Allergy Clin. Immunol. 136 (4): 952–961. doi:10.1016/j.jaci.2015.04.031. PMID 26044853.
- Osborn DA, Sinn JK (2013). "Prebiotics in infants for prevention of allergy". Cochrane Database Syst Rev (3): CD006474. doi:10.1002/14651858.CD006474.pub3. PMID 23543544.
- Zuccotti G, Meneghin F, Aceti A, Barone G, Callegari ML, Di Mauro A, Fantini MP, Gori D, Indrio F, Maggio L, Morelli L, Corvaglia L (2015). "Probiotics for prevention of atopic diseases in infants: systematic review and meta-analysis". Allergy. 70 (11): 1356–1371. doi:10.1111/all.12700. PMID 26198702.
- de Silva D, Geromi M, Panesar SS, Muraro A, Werfel T, Hoffmann-Sommergruber K, Roberts G, Cardona V, Dubois AE, Halken S, Host A, Poulsen LK, Van Ree R, Vlieg-Boerstra BJ, Agache I, Sheikh A (2014). "Acute and long-term management of food allergy: systematic review". Allergy. 69 (2): 159–167. doi:10.1111/all.12314. PMID 24215577.
- Zhang GQ, Hu HJ, Liu CY, Zhang Q, Shakya S, Li ZY (2016). "Probiotics for Prevention of Atopy and Food Hypersensitivity in Early Childhood: A PRISMA-Compliant Systematic Review and Meta-Analysis of Randomized Controlled Trials". Medicine. 95 (8): e2562. doi:10.1097/MD.0000000000002562. PMC . PMID 26937896.