Wheat Allergy

Earn CME/CE in your profession:


Continuing Education Activity

The wheat allergy is either IgE-mediated or non-IgE-mediated allergic reaction to wheat proteins. The result can be life-threatening and can lead to an anaphylactic reaction. Celiac disease is an example of a non-IgE-mediated wheat allergy. This activity reviews the evaluation and management of wheat allergy and highlights the role of the interprofessional team in educating patients about their condition.

Objectives:

  • Review the history and physical exam findings associated with a wheat allergy.

  • Describe the evaluation of a patient with a wheat allergy.

  • Explain the treatment considerations for patients with a wheat allergy.

  • Summarize the importance of improving care coordination among interprofessional team members to improve outcomes for patients affected by wheat allergy.

Introduction

Bread wheat, also known as Triticum aestivum, is one of the commonly grown crops worldwide.[1] It can be grown worldwide because it grows easily in different climates, and has a high nutritional value, high palatability, and can be processed into many foods and drinks.[1][2] However, despite these benefits, common wheat is recognized as an immune-mediated food allergen because it activates immunoglobulin E (IgE) and non-IgE immune responses.[1][2] IgE-mediated reactions to wheat are well-known and can be due to either ingestion (food allergy) or inhalation (respiratory allergy).

Etiology

The etiology of a wheat allergy is either IgE-mediated or non-IgE-mediated allergic reaction to wheat proteins.[3] The result can be life-threatening and can lead to an anaphylactic reaction. Celiac disease is a non-IgE-mediated immune response. IgE mediated reactions are characterized by the presence of wheat-specific IgE antibodies, and can be lethal. Non-IgE mediated reactions cause chronic eosinophilic and lymphocytic infiltration of the gastrointestinal tract. IgE-mediated reactions to wheat can be related to wheat ingestion or wheat inhalation. A food allergy to wheat is more common in children and can be associated with severe anaphylaxis and wheat-dependent exercise-induced anaphylaxis (WDEIA). An inhalation-induced IgE mediated wheat allergy can cause baker’s asthma, which is a common occupational disease in bakers who have significant repetitive exposure to wheat flour. Non-IgE mediated food allergy reactions to wheat are mainly eosinophilic esophagitis or eosinophilic gastritis, which are both characterized by chronic eosinophilic inflammation.

Epidemiology

The prevalence of confirmed (via food challenge), IgE-mediated food allergy to wheat is unknown. The prevalence of wheat-based food allergy is likely in the range of 0.2% to 1%.[1] Children have a higher prevalence of wheat allergies compared to adults and are more likely to develop an allergy if wheat is introduced after six months of life.[1][4] Children typically outgrow their allergy, and about 65% have a resolution by the age of 12.[5] The prevalence of celiac disease, a non-IgE-mediated food allergy to wheat, is approximately 1% to 2% in the United States.[6][7][8]

Pathophysiology

Wheat allergy is the manifestation of mediator release, such as histamine, platelet activator factor, and leukotrienes, from mast cells and basophils.[1][9][10] The IgE production is thought to be due to a breach of oral tolerance, and as a result, of type 2 helper T cell-biased immune dysregulation that causes sensitization and B-cell IgE production.[11][12][13][14][15] Allergens found in wheat flour are alpha-purothionin, alpha-amylase/trypsin inhibitor, peroxidase, thioredoxin, lipid-protein transfer, serine proteinase inhibitor, thaumatin-like protein (TLP), gliadin, thiol reductase, 1-cys-peroxiredoxin, and serine protease-like inhibitor.[1]

Celiac disease is characterized by a specific autoantibody against tissue transglutaminase 2 (anti-tTG2), endomysium, and deamidated gliadin peptide.[16][17] When gliadin peptides pass through the epithelial barrier, they activate CD4 T-lymphocytes which produce high levels of pro-inflammatory cytokines.[6] The pro-inflammatory cytokines activate T-helper 1 pattern interferon-gamma and a T-helper 2 pattern causing an expansion of B-lymphocytes, subsequently differentiating into plasma cells that secrete anti-gliadin and anti-tissue-transglutaminase antibodies.[6][18] For celiac disease, the histological changes that are expected in the small intestines are an increased number of intraepithelial lymphocytes, elongation of crypts, and partial to total villous atrophy.[16][19]

History and Physical

Providers should obtain a comprehensive history, including whether the patient has had a prior food allergic reaction to wheat or had a respiratory allergy to wheat flour.[5][20][21] If a patient develops symptoms anywhere from one to three hours after the exposure to wheat, the allergy to wheat should be confirmed by measuring IgE specific to wheat by skin prick test (SPT) or via serum IgE. An additional history that is important includes occupational history including current and past employment.[21]

Symptoms consistent with a wheat allergy would include urticaria, angioedema, asthma, allergic rhinitis, abdominal pain, vomiting, acute exacerbation of atopic dermatitis, or exercise-induced anaphylaxis.[1][22][23][24]

Patients with wheat dependent exercise-induced anaphylaxis (WDEIA) usually have symptoms that include pruritus, urticaria, angioedema, flushing, shortness of breath, dysphagia, chest tightness, profuse sweating, syncope, headache, diarrhea, nausea, throat closing, abdominal pain, and hoarseness that occurs during intense physical exercise following wheat intake in the prior four hours before symptom onset.[1][25]

Those with celiac disease will present with diarrhea, constipation, bloating, abdominal pain, anorexia, flatulence, weight loss, poor growth in childhood, anemia, dermatitis herpetiformis, fatigue, and even osteoporosis.[16]

Evaluation

As above, anyone who develops an allergic reaction to wheat exposure should be checked for IgE specific to wheat via a skin prick test or serum IgE.[1] A positive test for a serum IgE to wheat without a clinical history of symptoms after wheat exposure is not enough to diagnose a wheat allergy as people can be sensitive to wheat but can tolerate exposure to wheat.[1][26][27] Moreover, diagnosis of an allergy based on wheat flour extract cannot differentiate between those having a respiratory allergy versus those suffering from a food allergy to wheat.[1] The exact level of IgE that predicts whether the reaction is a true allergy in over 90% of patients is not well known.[1] Generally, children with even high levels of IgE can tolerate certain foods when undergoing an oral food challenge, and thus it is difficult to correlate an IgE level to a wheat allergy.[1][5][28][29][30] Moreover, an evaluation of a wheat allergy should be done by a health care provider as there is a potential risk of anaphylaxis and the need for epinephrine.[1][22][23]

For those being worked up for WDEIA, SPT or specific IgE to wheat, gluten, and omega-5-gliadin should be ordered.[1][20][31][32]

For patients being evaluated for baker's asthma, the lower limit with a positive predictive value of 100 percent was 2.32 kU/L for specific wheat IgE and 5.0 mm for wheat on SPT with wheat flour extracts.[1][33] The gold standard to confirm the diagnosis of wheat-induced occupational allergy is a bronchial challenge test which consists of a nebulized aqueous flour solution in increasing concentrations (0.01, 0.1, 10, and 100 mg/mL) or by inhaling wheat flour dust.[1] Baker's asthma is diagnosed if a bronchial challenge test induces at minimum a 20% decrease in forced expiratory volume in one second (FEV1) or a three-fold increase in bronchial hyperreactivity with an increase in sputum eosinophilia.[1][34]

For celiac disease, measurement of serum immunoglobulin A antibody to tissue transglutaminase (anti-tTG) should be the first screening test ordered.[16] For those with IgA deficiency, deamidated gliadin peptides-antibody of the IgG class can be used as an initial screening test.[16] An IgA anti-endomysial antibody has a 98% specificity for active celiac disease and should be ordered as a confirmatory test.[16][35]

Treatment / Management

Primary treatment and management of wheat allergies is avoidance of both food and inhaled wheat allergens.[1] For celiac disease, a lifelong, gluten-free diet is the current treatment option.[6]

In cases of exposure and an anaphylactic reaction, the administration of epinephrine is the lifesaving treatment. Epinephrine comes in either a 0.15 or 0.3 mg intramuscular injection and is typically injected into the lateral thigh. All patients should go to the emergency room for further evaluation and antihistamines, glucocorticoids, and beta-agonist are additional secondary treatment options.[1][23] Additional treatments include immunotherapy such as oral immunotherapy (OIT), sublingual immunotherapy (SLIT), and epicutaneous immunotherapy (EPIT).[1][36] OIT and SLIT both utilize the principle of gradually increasing the amount of food ingested leading to desensitization and thus hopefully helping to avoid experiencing an allergic reaction. EPIT utilizes a skin patch to deliver an allergen to the patient. Those with WDEIA require epinephrine and can avoid symptoms by, avoiding exercising within four to six hours after wheat ingestion, avoid exercising alone or in hot weather/pollen season, and carrying emergency medication.[1][20]

Differential Diagnosis

The differential diagnoses for a wheat allergy are broad and include:[1]

  • Non-IgE-mediated food allergy (food protein-induced enterocolitis)
  • Flush syndrome (carcinoid, postmenopausal, chlorpropamide-alcohol, autonomic epilepsy)
  • Restaurant syndromes (sodium glutamate, sulfites, scombroid)
  • Non-anaphylactic shock (hemorrhagic, cardiac, endotoxic, monoclonal gammopathy)
  • Syndromes with excessive endogenous production of histamine (idiopathic angioedema, mastocytosis, urticaria pigmentosa, basophil leukemia, promyelocytic acute leukemia, hydatid cyst)
  • Nonorganic syndromes (panic attack, Munchausen, vocal cord dysfunction, hysteric bolus, anorexia nervosa)
  • Hereditary angioedema
  • Anaphylaxis due to progesterone
  • Urticarial vasculitis
  • Pheochromocytoma
  • Hyper IgE syndrome
  • Seizure
  • Stroke
  • Pseudo-anaphylaxis
  • Redman syndrome
  • Irritable bowel syndrome

Prognosis

IgE-mediated food allergy and wheat-dependent exercise-induced anaphylaxis (WDEIA) are associated with impaired quality of life and significant morbidity. IgE-mediated wheat allergy in adults is usually benign. For those with celiac disease, adherence to a gluten-free diet might prevent morbidity and mortality associated with celiac disease.[16] The prognosis of those celiac disease patients who do not respond to gluten withdrawal and corticosteroid treatment is generally poor.

Complications

Conditions associated with celiac disease include type 1 diabetes, autoimmune thyroid disorders, autoimmune hepatitis, and neurological disorders such as epilepsy.[6] Complications of celiac disease can include but are not limited to:[16]

  • Anemia
  • Anxiety
  • Arthralgia
  • Arthritis
  • Dental enamel hypoplasia
  • Delayed puberty
  • Depression
  • Fatigue
  • Infertility
  • Osteoporosis
  • Pancreatitis
  • Peripheral neuropathy
  • Short stature
  • Other complications of celiac disease can include enteropathy-associated intestinal T-cell lymphoma, small bowel adenocarcinoma, and non-Hodgkin lymphoma[6]

Consultations

Important consultation for a wheat allergy includes an allergy and immunology provider, gastroenterologist, and nutritionist. If a patient is having gastrointestinal (GI) symptoms, a gastroenterologist can help determine differential diagnoses, conduct further testing, and determine the etiology of the symptoms. An allergist can do skin and blood testing to make the diagnosis and guide treatment options, such as immunotherapy. Additional consultations that would be helpful would be a nutritionist who can guide dietary changes that need to be made to avoid wheat from one's diet.

Deterrence and Patient Education

Patients who have signs or symptoms of a wheat allergy should see a doctor as soon as possible as it can be a life-threatening disease. Those who are already diagnosed should make sure they avoid wheat and always carry epinephrine. A medical identification bracelet that describes the allergy should be worn all the time whenever a patient leaves home and needs emergency care can help if he/she experiences anaphylaxis and can't communicate. Parents of children who have a wheat allergy must make sure that anyone who takes care of the children, including the principal, teachers, and nurse at school or child care, knows about the allergy and the signs of wheat exposure. Following up with an allergist can offer treatment options such as immunotherapy. Those with celiac disease should maintain a gluten-free diet to avoid symptoms and follow up with a gastroenterologist.

Enhancing Healthcare Team Outcomes

A wheat allergy can be life-threatening, and it is vital that patients carry epinephrine. Patients should follow up with an allergist for treatment goals. Patients will also benefit from a gastroenterology follow-up as patients frequently have GI symptoms, especially if they have celiac disease. Wheat allergies are just one of the many allergic reactions that a patient can face. An interprofessional allergy clinic can improve families' ability to manage allergies and reduce allergic reactions.[37] (Level II)


Details

Author

Nicolas Patel

Updated:

6/25/2023 6:03:23 PM

Looking for an easier read?

Click here for a simplified version

References


[1]

Cianferoni A. Wheat allergy: diagnosis and management. Journal of asthma and allergy. 2016:9():13-25. doi: 10.2147/JAA.S81550. Epub 2016 Jan 29     [PubMed PMID: 26889090]


[2]

Fasano A, Sapone A, Zevallos V, Schuppan D. Nonceliac gluten sensitivity. Gastroenterology. 2015 May:148(6):1195-204. doi: 10.1053/j.gastro.2014.12.049. Epub 2015 Jan 9     [PubMed PMID: 25583468]


[3]

Pasha I, Saeed F, Sultan MT, Batool R, Aziz M, Ahmed W. Wheat Allergy and Intolerence; Recent Updates and Perspectives. Critical reviews in food science and nutrition. 2016:56(1):13-24. doi: 10.1080/10408398.2012.659818. Epub     [PubMed PMID: 24915366]

Level 3 (low-level) evidence

[4]

Poole JA, Barriga K, Leung DY, Hoffman M, Eisenbarth GS, Rewers M, Norris JM. Timing of initial exposure to cereal grains and the risk of wheat allergy. Pediatrics. 2006 Jun:117(6):2175-82     [PubMed PMID: 16740862]


[5]

Keet CA, Matsui EC, Dhillon G, Lenehan P, Paterakis M, Wood RA. The natural history of wheat allergy. Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology. 2009 May:102(5):410-5. doi: 10.1016/S1081-1206(10)60513-3. Epub     [PubMed PMID: 19492663]


[6]

Parzanese I, Qehajaj D, Patrinicola F, Aralica M, Chiriva-Internati M, Stifter S, Elli L, Grizzi F. Celiac disease: From pathophysiology to treatment. World journal of gastrointestinal pathophysiology. 2017 May 15:8(2):27-38. doi: 10.4291/wjgp.v8.i2.27. Epub     [PubMed PMID: 28573065]


[7]

Rewers M. Epidemiology of celiac disease: what are the prevalence, incidence, and progression of celiac disease? Gastroenterology. 2005 Apr:128(4 Suppl 1):S47-51     [PubMed PMID: 15825126]


[8]

Fasano A. Where have all the American celiacs gone? Acta paediatrica (Oslo, Norway : 1992). Supplement. 1996 May:412():20-4     [PubMed PMID: 8783750]


[9]

Sampson HA. Food allergy. Part 1: immunopathogenesis and clinical disorders. The Journal of allergy and clinical immunology. 1999 May:103(5 Pt 1):717-28     [PubMed PMID: 10329801]


[10]

Lee LA, Burks AW. Food allergies: prevalence, molecular characterization, and treatment/prevention strategies. Annual review of nutrition. 2006:26():539-65     [PubMed PMID: 16602930]


[11]

Chehade M, Mayer L. Oral tolerance and its relation to food hypersensitivities. The Journal of allergy and clinical immunology. 2005 Jan:115(1):3-12; quiz 13     [PubMed PMID: 15637539]


[12]

Heyman M. Symposium on 'dietary influences on mucosal immunity'. How dietary antigens access the mucosal immune system. The Proceedings of the Nutrition Society. 2001 Nov:60(4):419-26     [PubMed PMID: 12069393]


[13]

Iwasaki A. Mucosal dendritic cells. Annual review of immunology. 2007:25():381-418     [PubMed PMID: 17378762]


[14]

Dahan S, Roth-Walter F, Arnaboldi P, Agarwal S, Mayer L. Epithelia: lymphocyte interactions in the gut. Immunological reviews. 2007 Feb:215():243-53. doi: 10.1111/j.1600-065X.2006.00484.x. Epub     [PubMed PMID: 17291293]


[15]

Mowat AM. Anatomical basis of tolerance and immunity to intestinal antigens. Nature reviews. Immunology. 2003 Apr:3(4):331-41     [PubMed PMID: 12669023]


[16]

Leonard MM, Sapone A, Catassi C, Fasano A. Celiac Disease and Nonceliac Gluten Sensitivity: A Review. JAMA. 2017 Aug 15:318(7):647-656. doi: 10.1001/jama.2017.9730. Epub     [PubMed PMID: 28810029]


[17]

Ludvigsson JF, Leffler DA, Bai JC, Biagi F, Fasano A, Green PH, Hadjivassiliou M, Kaukinen K, Kelly CP, Leonard JN, Lundin KE, Murray JA, Sanders DS, Walker MM, Zingone F, Ciacci C. The Oslo definitions for coeliac disease and related terms. Gut. 2013 Jan:62(1):43-52. doi: 10.1136/gutjnl-2011-301346. Epub 2012 Feb 16     [PubMed PMID: 22345659]


[18]

Björck S, Lindehammer SR, Fex M, Agardh D. Serum cytokine pattern in young children with screening detected coeliac disease. Clinical and experimental immunology. 2015 Feb:179(2):230-5. doi: 10.1111/cei.12454. Epub     [PubMed PMID: 25212572]


[19]

Hill PG, Holmes GK. Coeliac disease: a biopsy is not always necessary for diagnosis. Alimentary pharmacology & therapeutics. 2008 Apr 1:27(7):572-7. doi: 10.1111/j.1365-2036.2008.03609.x. Epub 2008 Jan 11     [PubMed PMID: 18194500]


[20]

Scherf KA, Brockow K, Biedermann T, Koehler P, Wieser H. Wheat-dependent exercise-induced anaphylaxis. Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology. 2016 Jan:46(1):10-20. doi: 10.1111/cea.12640. Epub     [PubMed PMID: 26381478]


[21]

Quirce S, Diaz-Perales A. Diagnosis and management of grain-induced asthma. Allergy, asthma & immunology research. 2013 Nov:5(6):348-56. doi: 10.4168/aair.2013.5.6.348. Epub 2013 Jun 25     [PubMed PMID: 24179680]


[22]

Cianferoni A, Khullar K, Saltzman R, Fiedler J, Garrett JP, Naimi DR, Spergel JM. Oral food challenge to wheat: a near-fatal anaphylaxis and review of 93 food challenges in children. The World Allergy Organization journal. 2013 Aug 21:6(1):14. doi: 10.1186/1939-4551-6-14. Epub 2013 Aug 21     [PubMed PMID: 23965733]


[23]

Cianferoni A, Muraro A. Food-induced anaphylaxis. Immunology and allergy clinics of North America. 2012 Feb:32(1):165-95. doi: 10.1016/j.iac.2011.10.002. Epub 2011 Nov 21     [PubMed PMID: 22244239]


[24]

Salcedo G, Quirce S, Diaz-Perales A. Wheat allergens associated with Baker's asthma. Journal of investigational allergology & clinical immunology. 2011:21(2):81-92; quiz 94     [PubMed PMID: 21462797]


[25]

Du Toit G. Food-dependent exercise-induced anaphylaxis in childhood. Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology. 2007 Aug:18(5):455-63     [PubMed PMID: 17617816]


[26]

Sander I, Raulf-Heimsoth M, Düser M, Flagge A, Czuppon AB, Baur X. Differentiation between cosensitization and cross-reactivity in wheat flour and grass pollen-sensitized subjects. International archives of allergy and immunology. 1997 Apr:112(4):378-85     [PubMed PMID: 9104794]


[27]

Jones SM, Magnolfi CF, Cooke SK, Sampson HA. Immunologic cross-reactivity among cereal grains and grasses in children with food hypersensitivity. The Journal of allergy and clinical immunology. 1995 Sep:96(3):341-51     [PubMed PMID: 7560636]


[28]

Niggemann B, Sielaff B, Beyer K, Binder C, Wahn U. Outcome of double-blind, placebo-controlled food challenge tests in 107 children with atopic dermatitis. Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology. 1999 Jan:29(1):91-6     [PubMed PMID: 10051707]

Level 1 (high-level) evidence

[29]

Niggemann B, Rolinck-Werninghaus C, Mehl A, Binder C, Ziegert M, Beyer K. Controlled oral food challenges in children--when indicated, when superfluous? Allergy. 2005 Jul:60(7):865-70     [PubMed PMID: 15932374]


[30]

Perry TT, Matsui EC, Conover-Walker MK, Wood RA. Risk of oral food challenges. The Journal of allergy and clinical immunology. 2004 Nov:114(5):1164-8     [PubMed PMID: 15536426]


[31]

Palosuo K, Alenius H, Varjonen E, Koivuluhta M, Mikkola J, Keskinen H, Kalkkinen N, Reunala T. A novel wheat gliadin as a cause of exercise-induced anaphylaxis. The Journal of allergy and clinical immunology. 1999 May:103(5 Pt 1):912-7     [PubMed PMID: 10329828]


[32]

Morita E, Matsuo H, Mihara S, Morimoto K, Savage AW, Tatham AS. Fast omega-gliadin is a major allergen in wheat-dependent exercise-induced anaphylaxis. Journal of dermatological science. 2003 Nov:33(2):99-104     [PubMed PMID: 14581135]


[33]

van Kampen V, Rabstein S, Sander I, Merget R, Brüning T, Broding HC, Keller C, Müsken H, Overlack A, Schultze-Werninghaus G, Walusiak J, Raulf-Heimsoth M. Prediction of challenge test results by flour-specific IgE and skin prick test in symptomatic bakers. Allergy. 2008 Jul:63(7):897-902. doi: 10.1111/j.1398-9995.2008.01646.x. Epub     [PubMed PMID: 18588556]


[34]

Wiszniewska M, Nowakowska-Świrta E, Pałczyński C, Walusiak-Skorupa J. Diagnosing of bakers' respiratory allergy: is specific inhalation challenge test essential? Allergy and asthma proceedings. 2011 Mar-Apr:32(2):111-8. doi: 10.2500/aap.2011.32.3422. Epub     [PubMed PMID: 21439164]


[35]

Giersiepen K, Lelgemann M, Stuhldreher N, Ronfani L, Husby S, Koletzko S, Korponay-Szabó IR, ESPGHAN Working Group on Coeliac Disease Diagnosis. Accuracy of diagnostic antibody tests for coeliac disease in children: summary of an evidence report. Journal of pediatric gastroenterology and nutrition. 2012 Feb:54(2):229-41. doi: 10.1097/MPG.0b013e318216f2e5. Epub     [PubMed PMID: 22266486]


[36]

Jones SM, Burks AW, Dupont C. State of the art on food allergen immunotherapy: oral, sublingual, and epicutaneous. The Journal of allergy and clinical immunology. 2014 Feb:133(2):318-23. doi: 10.1016/j.jaci.2013.12.1040. Epub     [PubMed PMID: 24636471]


[37]

Kapoor S, Roberts G, Bynoe Y, Gaughan M, Habibi P, Lack G. Influence of a multidisciplinary paediatric allergy clinic on parental knowledge and rate of subsequent allergic reactions. Allergy. 2004 Feb:59(2):185-91     [PubMed PMID: 14763932]