Alpha-gal syndrome


Alpha-gal syndrome, also known as alpha-gal allergy or mammalian meat allergy, is a type of acquired allergy characterized by a delayed onset of symptoms after ingesting mammalian meat. The condition results from past exposure to certain tick bites and was first reported in 2002.
Symptoms of the allergy vary greatly between individuals and include rash, hives, nausea or vomiting, difficulty breathing, drop in blood pressure, dizziness or faintness, diarrhea, severe stomach pain, and possible anaphylaxis. Death has been reported.
Alpha-gal allergy is a reaction to the carbohydrate galactose-alpha-1,3-galactose, whereby the body is overloaded with immunoglobulin E antibodies on exposure to the carbohydrate. Anti-gal is a human natural antibody that interacts specifically with the mammalian carbohydrate structure Galα1-3Galβ1-4GlcNAc-R. The alpha-gal molecule is found in all mammals except catarrhines, the taxonomic branch that includes humans.
In 2006, researchers Thomas Platts-Mills and Scott Commins attempted to discover why some people were allergic to the cancer drug cetuximab, and discovered that these individuals had IgE antibodies in their blood that were specifically targeted to the portion of cetuximab which contained the alpha-gal carbohydrate. When Platts-Mills was bitten by a tick and developed alpha-gal allergies, his team concluded that a link existed between tick bites and the allergy. They found that the IgE antibody response to the mammalian oligosaccharide epitope alpha-gal was associated with both the immediate-onset anaphylaxis during first exposure to intravenous cetuximab and the delayed-onset anaphylaxis 3 to 6 hours after ingestion of mammalian food products, such as beef or pork.
Bites from specific tick species, such as the Lone Star tick '' in the US and the paralysis tick in Australia, that can transfer this carbohydrate to a victim have been implicated in the development of this delayed allergic response to consumption of mammalian meat products. Healthcare providers recommend that sufferers avoid food products containing beef, pork, lamb, venison, rabbit, and offal to avoid triggering an allergic reaction. Some afflicted individuals are so sensitive to alpha-gal that the allergy can cross-react with mammalian gelatin and even some dairy products. Individuals with an alpha-gal allergy do not need to become strict vegetarians because reptile meats, poultryincluding red meat from ostriches, emus, and other ratitesand seafood naturally do not contain alpha-gal. Increasing evidence now suggests reactions to certain substances with traces of alpha-gal used in the preparation of certain medications, including nonsteroidal anti-inflammatory drugs and other analgesics and pain medications.
Alpha-gal allergy has been reported in 17 countries on all six continents where humans are bitten by ticks, particularly the United States and Australia. Alpha-gal allergies are the first known food allergies that present the possibility of delayed anaphylaxis. They are also the first known food-related allergies associated with a carbohydrate, rather than a protein.

Signs and symptoms

A typical allergic reaction to alpha-gal has a delayed onset, occurring 3–8 hours after consuming mammalian meat products. However, there have been instances of the onset of symptoms occurring within 2 hours. After the delayed onset, the allergic response is like most food allergies, and especially an IgE-mediated allergy, including severe whole-body itching, hives, angioedema, gastrointestinal upset, and possible anaphylaxis. Anaphylactic reactions are seen in approximately 60% of afflicted individuals.
There have been cases where gastrointestinal symptoms arise without pruritus, hives, or other skin involvement. This presentation is not typical of food allergies, which can make initial suspicion of alpha-gal syndrome less likely. In 70% of cases, the reaction is accompanied by respiratory distress and is particularly harmful to those with asthma. However, not every exposure to alpha-gal results in an allergic reaction for some people with the allergy.
Symptoms and overall reactions can vary greatly among individuals with alpha-gal syndrome. Other factors, including exercise and alcohol consumption, can potentially affect an individual's symptoms and overall reactivity to alpha-gal. Increased risk has also been discovered in those without type B or type AB blood, as the type B blood antigen is similar to alpha-gal and may confer some level of protection.
The severity of symptoms and overall reaction to alpha-gal have been found to correlate with the amount of alpha-gal carbohydrate in the ingested food or drug.

Cause and mechanism

Alpha-gal allergies develop after a person has been bitten by the lone star tick or the black-legged tick in the United States, the European castor bean tick, the paralysis tick or Ixodes australiensis in Australia, Haemaphysalis longicornis in Japan, or a currently unknown tick in South Africa, possibly Amblyomma hebraeum''. Alpha-gal is not naturally present in apes, Old World monkeys, or humans, but is in all other mammals. If a tick feeds on another mammal, the alpha-gal remains in its alimentary tract. The role of the lone star tick, commonly found throughout the US, in the context of tick bites has been confirmed using an alpha-gal knockout mouse model.
The tick injects the alpha-gal into a person's skin with its bite. Recent research has shown that saliva from the lone star tick contains alpha-gal, and that saliva is injected into the bloodstream. Researchers still do not know which specific component of tick saliva causes the reaction. The immune system then releases a flood of IgE antibodies to fight this foreign sugar. After this reaction, the future intake of mammalian meat with the same alpha-gal causes an allergic reaction. Symptoms of the allergy reaction are caused by too many IgE antibodies attacking the allergen namely the alpha-gal. Other types of ticks are suspected of causing similar problems. Only a small percentage of people—whether children or adults—will acquire a red meat allergy after receiving a bite from a Lone Star tick.
A 2012 preliminary study found unexpectedly high rates of alpha-gal allergy in the western and north-central parts of the United States. This suggests that unknown tick species may spread the allergy. The study found alpha-gal allergy cases in Hawaii, where no ticks identified with the allergies live. Human factors were suggested, but no specific examples were provided.
Blood thinners derived from porcine intestine and replacement heart valves derived from porcine tissue may also contain alpha-gal. Alpha gal is found on the fragment-antigen binding fragment of the recombinant monoclonal cetuximab antibody used in the immunotherapy treatment of metastatic colon cancer. Immediate hypersensitivities and reactions, specifically concentrated in the southern part of the United States, can be seen from the alpha-gal components of this anti-cancer drug. Increasing evidence now suggests reactions to certain substances with traces of alpha-gal used in the preparation of certain medications, including nonsteroidal anti-inflammatory drugs and other analgesics and pain medications.
Anaphylactic transfusion reactions have been reported in patients with presumed alpha-gal syndrome who had type O blood and received group B plasma or platelets. The B blood group antigen is antigenically similar to Galactose-alpha-1,3-Galactose.

Diagnosis

Diagnosis begins with initial suspicion of alpha-gal syndrome following a thorough review of an individual's medical history and clinical symptoms. Research has shown that in the USA it takes on average more than 7 years from time of symptom onset to receive a correct diagnosis. Regarding laboratory testing, diagnosis tends to be difficult, and no specific test is recommended over others.
A blood test for the specific antibody, IgE, to the alpha-gal carbohydrate, is commonly used for diagnosis in clinical practice. Typically, a level of 1% for IgE specific for alpha-gal out of total IgE in the body has been identified in patients with alpha-gal syndrome. Traditional skin-prick allergy tests for allergy to meat may give a false-negative answer and are not generally considered reliable. Skin and basophil activation tests with cetuximab are the most sensitive, but high costs limit their use.
In certain instances in which a person does not present with the typical symptoms and history of alpha-gal syndrome but is found to have elevated alpha-gal IgE levels, improvement with avoidance of red meat can be diagnostic, as well.

Prognosis

There is no cure for alpha-gal; the main form of management is abstaining from mammalian meat, including lamb, beef, pork, and other mammalian products if necessary. These products have been found to have the highest risk of reaction, whereas dairy products present a much lower risk. Avoidance of dairy is not generally recommended, as most afflicted individuals do not have reactions to dairy consumption.
Unlike most food allergies, in some people, the alpha-gal allergy may improve over time as long as another tick does not bite the person. It has been found that by avoiding further tick bites, serum IgE levels decrease. The recovery period can take 8 months to 5 years.

Treatment

In addition to avoiding triggers, such as mammalian meat, treatment aims to alleviate symptoms and is highly dependent on severity. If an allergic individual who only experiences relatively mild symptoms consumes food containing alpha-gal, then treatment with over-the-counter antihistamines may be acceptable. In cases where more severe reactions—like anaphylaxis—are observed, admission to a hospital for emergency treatment is necessary. In these situations, treatment is the same as for any anaphylactic reaction and necessitates epinephrine administration.