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PMID: 15526039 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The molecular basis for oat intolerance in patients with celiac disease.

PLoS medicine ·Vol. 1 ·No. 1 ·2004-10-00 ·Pages e1

Arentz-Hansen H, Fleckenstein B, Molberg Ø, Scott H, Koning F, Jung G, Roepstorff P, Lundin KE, Sollid LM

Abstract

Celiac disease is a small intestinal inflammatory disorder characterized by malabsorption, nutrient deficiency, and a range of clinical manifestations. It is caused by an inappropriate immune response to dietary gluten and is treated with a gluten-free diet. Recent feeding studies have indicated oats to be safe for celiac disease patients, and oats are now often included in the celiac disease diet. This study aimed to investigate whether oat intolerance exists in celiac disease and to characterize the cells and processes underlying this intolerance. We selected for study nine adults with celiac disease who had a history of oats exposure. Four of the patients had clinical symptoms on an oats-containing diet, and three of these four patients had intestinal inflammation typical of celiac disease at the time of oats exposure. We established oats-avenin-specific and -reactive intestinal T-cell lines from these three patients, as well as from two other patients who appeared to tolerate oats. The avenin-reactive T-cell lines recognized avenin peptides in the context of HLA-DQ2. These peptides have sequences rich in proline and glutamine residues closely resembling wheat gluten epitopes. Deamidation (glutamine-->glutamic acid conversion) by tissue transglutaminase was involved in the avenin epitope formation. We conclude that some celiac disease patients have avenin-reactive mucosal T-cells that can cause mucosal inflammation. Oat intolerance may be a reason for villous atrophy and inflammation in patients with celiac disease who are eating oats but otherwise are adhering to a strict gluten-free diet. Clinical follow-up of celiac disease patients eating oats is advisable.

MeSH Terms
Atrophy Avena Celiac Disease/physiopathology Diet Humans Inflammation Intestinal Mucosa/immunology,pathology Plant Proteins/immunology Prolamins T-Lymphocytes/immunology
Chemicals
Plant Proteins Prolamins
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Arentz-Hansen Helene
Institute of Immunology, Rikshospitalet University Hospital, University of Oslo, Oslo, Norway.
Fleckenstein Burkhard
Molberg Øyvind
Scott Helge
Koning Frits
Jung Günther
Roepstorff Peter
Lundin Knut E A
Sollid Ludvig M
References (24)
24 references, click to expand
  1. The intestinal T cell response to alpha-gliadin in adult celiac disease is focused on a single deamidated glutamine targeted by tissue transglutaminase.
    J Exp Med. 2000 Feb 21;191(4):603-12 PMID: 10684852
  2. The histopathology of coeliac disease: time for a standardized report scheme for pathologists.
    Eur J Gastroenterol Hepatol. 1999 Oct;11(10):1185-94 PMID: 10524652
  3. High selectivity of human tissue transglutaminase for immunoactive gliadin peptides: implications for celiac sprue.
    Biochemistry. 2002 Jan 8;41(1):386-93 PMID: 11772038
  4. No harm from five year ingestion of oats in coeliac disease.
    Gut. 2002 Mar;50(3):332-5 PMID: 11839710
  5. Specificity of tissue transglutaminase explains cereal toxicity in celiac disease.
    J Exp Med. 2002 Mar 4;195(5):643-9 PMID: 11877487
  6. Celiac lesion T cells recognize epitopes that cluster in regions of gliadins rich in proline residues.
    Gastroenterology. 2002 Sep;123(3):803-9 PMID: 12198706
  7. Coeliac disease: dissecting a complex inflammatory disorder.
    Nat Rev Immunol. 2002 Sep;2(9):647-55 PMID: 12209133
  8. Gliadin T cell epitope selection by tissue transglutaminase in celiac disease. Role of enzyme specificity and pH influence on the transamidation versus deamidation process.
    J Biol Chem. 2002 Sep 13;277(37):34109-16 PMID: 12093810
  9. Structural basis for gluten intolerance in celiac sprue.
    Science. 2002 Sep 27;297(5590):2275-9 PMID: 12351792
  10. Avenin fails to induce a Th1 response in coeliac tissue following in vitro culture.
    Gut. 2003 Jan;52(1):47-52 PMID: 12477758
  11. Adult coeliac patients do tolerate large amounts of oats.
    Eur J Clin Nutr. 2003 Jan;57(1):163-9 PMID: 12548312
  12. Oats and the gluten-free diet.
    J Am Diet Assoc. 2003 Mar;103(3):376-9 PMID: 12616264
  13. Intestinal T-cell responses to high-molecular-weight glutenins in celiac disease.
    Gastroenterology. 2003 Aug;125(2):337-44 PMID: 12891534
  14. Characterization of cereal toxicity for celiac disease patients based on protein homology in grains.
    Gastroenterology. 2003 Oct;125(4):1105-13 PMID: 14517794
  15. Effect of an oats-containing gluten-free diet on symptoms and quality of life in coeliac disease. A randomized study.
    Scand J Gastroenterol. 2004 Jan;39(1):27-31 PMID: 14992558
  16. Structural basis for HLA-DQ2-mediated presentation of gluten epitopes in celiac disease.
    Proc Natl Acad Sci U S A. 2004 Mar 23;101(12):4175-9 PMID: 15020763
  17. Oats to children with newly diagnosed coeliac disease: a randomised double blind study.
    Gut. 2004 May;53(5):649-54 PMID: 15082581
  18. Proposal for a common nomenclature for sequence ions in mass spectra of peptides.
    Biomed Mass Spectrom. 1984 Nov;11(11):601 PMID: 6525415
  19. T cells from the small intestinal mucosa of a DR4, DQ7/DR4, DQ8 celiac disease patient preferentially recognize gliadin when presented by DQ8.
    Hum Immunol. 1994 Dec;41(4):285-91 PMID: 7883596
  20. A comparison of diets with and without oats in adults with celiac disease.
    N Engl J Med. 1995 Oct 19;333(16):1033-7 PMID: 7675045
  21. Absence of oats toxicity in adult coeliac disease.
    BMJ. 1996 Nov 23;313(7068):1300-1 PMID: 8942690
  22. Absence of toxicity of oats in patients with dermatitis herpetiformis.
    N Engl J Med. 1997 Dec 25;337(26):1884-7 PMID: 9407155
  23. Tolerance to oats in dermatitis herpetiformis.
    Gut. 1998 Oct;43(4):490-3 PMID: 9824575
  24. A trial of oats in children with newly diagnosed celiac disease.
    J Pediatr. 2000 Sep;137(3):361-6 PMID: 10969261
Article Info
Journal
PLoS medicine
Abbr.
PLoS Med
ISSN
1549-1676
Published
2004-10-00
Epub
2004-00-19
Pages
e1
Language
English
Region
United States
NLM ID
101231360
PMCID
PMC523824
Subset
IM
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