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Shapovalova N.S.

Saint-Petersburg State Pediatric Medical University, Saint-Petersburg, Russia

Novikova V.P.

Saint-Petersburg State Pediatric Medical University, Saint- Petersburg, Russia

Revnova M.O.

St. Petersburg State Pediatric Medical, Russia, 194044, St. Petersburg, St. Litovskaya 2

Nasyrov R.A.

St. Petersburg State Pediatric Medical, Russia, 194044, St. Petersburg, St. Litovskaya 2

Lapin S.V.

Pavlov First St. Petersburg State Medical University, Russia, 197022, St. Petersburg, St. Leo Tolstoy 6/8

Kholopova I.V.

Pavlov First St. Petersburg State Medical University, Russia, 197022, St. Petersburg, St. Leo Tolstoy 6/8

Klikunova K.A.

St. Petersburg State Pediatric Medical, Russia, 194044, St. Petersburg, St. Litovskaya 2

Predictive significance of hla-dq2.2 genotype for children with celiac disease

Authors:

Shapovalova N.S., Novikova V.P., Revnova M.O., Nasyrov R.A., Lapin S.V., Kholopova I.V., Klikunova K.A.

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To cite this article:

Shapovalova NS, Novikova VP, Revnova MO, Nasyrov RA, Lapin SV, Kholopova IV, Klikunova KA. Predictive significance of hla-dq2.2 genotype for children with celiac disease. Russian Journal of Evidence-Based Gastroenterology. 2018;7(4):6‑11. (In Russ.)
https://doi.org/10.17116/dokgastro201870416

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References:

  1. Bergseng E, Dorum S, Magnus O, Nielsen A, Nielsen M, Nygard S, Buus S, de Souza GA, Sollid LM. Different binding motifs of the celiac disease-associated HLA molecules DQ2.5, DQ2.2, and DQ7.5 revealed by relative quantitative proteomics of endogenous peptide repertoires. Immunogenetics. 2015;67:73-84.
  2. Husby S, Koletzko S, Korponay-Szabj IR, Mearin ML, Phillips A, Shamir R,Troncone R, Giersiepen K, Branski D, Catassi C, Lelgeman M, Maki M, Ribes-Koninckx C, Ventura A, Zimmer KP. European Society for Pediatric Gastroenterology,Hepatology, and Nutrition Guidelines for the Diagnosis of Coeliac Disease. JPGN. 2012;54(1):136-160.
  3. Parzanese I, Qehajaj D, Patrinicola F, Aralica M, Chiriva-Internati M, Stifter S, Elli L, Grizzi F. Celiac disease: From pathophysiology to treatment. WJGP. 2017;8(2):27-38.
  4. Abraham G, Rohmer A, Tye-Din JA, Inouye M. Genomic prediction of celiac disease targeting HLA-positive individuals.Genome Medicine. 2015 Jul 16;7(1):72.
  5. Karell K1, Louka AS, Moodie SJ, Ascher H, Clot F, Greco L, Ciclitira PJ, Sollid LM, Partanen J. HLA types in celiac disease patients not carrying the DQA1*05-DQB1*02 (DQ2) heterodimer: results from the European Genetics Cluster on Celiac Disease. Hum Immunol. 2003 Apr;64(4):469-477.
  6. Almeida LM, Gandolfi L, Pratesi R, Uenishi RH, de Almeida FC, Selleski N, de Medeiros Nóbrega YK. Presence of DQ2.2 Associated with DQ2.5 Increases the Risk for Celiac Disease. Autoimmune Diseases. 2016 Oct;6.
  7. Murray JA, Moore SB, Van Dyke CT, Lahr BD, Dierkhising RA, Zinsmeister AR, L. Melton J III, Kroning CM, El-Yousseff M, Czaja AJ. HLA DQ Gene Dosage and Risk and Severity of Celiac Disease. Clin Gastroenterol Hepatol. 2007 December; 5(12):1406-1412.
  8. Vader W, Stepniak D, Kooy Y, Mearin L, Thompson A, van Rood JJ, Spaenij L, Koning F. The HLA-DQ2 gene dose effect in celiac disease is directly related to the magnitude and breadth of gluten-specific T-cell responses. Proc Natl Acad Sci USA. 2003;100:12390-12395.
  9. Zubillaga P, Vidales MC, Zubillaga I, Ormaechea V, Garcia-Urkia N, Vitoria JC. HLA-DQA1 and HLA-DQB1 genetic markers and clinical presentation in celiac disease. J Pediatr Gastroenterol Nutr. 2002;34:548-554.
  10. Al-Toma A, Goerres MS, Meijer JW, Pena AS, Crusius JB, Mulder CJ. Human leukocyte antigen-DQ2 homozygosity and the development of refractory celiac disease and enteropathy-associated T-cell lymphoma. Clin Gastroenterol Hepatol. 2006;4:315-319.
  11. Revnova MO, Novikova VP, Shapovalova NS, Kalinina EYu, Lapin SV, Kholopova IV. Genotypes of HLA II-DQ in children with celiac disease with high and low levels of tissue transglutaminase antibodies. Med immunol. 2015;17(SS):140. (In Russ)

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