The molecular basis for oat intolerance in patients with Celiac disease

被引:181
作者
Arentz-Hansen, H
Fleckenstein, B
Molberg, O
Scott, H
Koning, F
Jung, G
Roepstorff, P
Lundin, KEA
Sollid, LM [1 ]
机构
[1] Univ Oslo, Rikshosp, Univ Hosp, Inst Immunol, N-0027 Oslo, Norway
[2] Univ So Denmark, Dept Biochem & Mol Biol, Odense, Denmark
[3] Univ Oslo, Rikshosp, Univ Hosp, Inst Pathol, N-0027 Oslo, Norway
[4] Leiden Univ, Med Ctr, Dept Immunohematol & Blood Tranfus, Leiden, Netherlands
[5] Univ Tubingen, Inst Organ Chem, D-7400 Tubingen, Germany
[6] Univ Oslo, Rikshosp, Univ Hosp, Dept Med, N-0027 Oslo, Norway
关键词
D O I
10.1371/journal.pmed.0010001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background 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. Methods and Findings 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. Conclusions 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.
引用
收藏
页码:84 / 92
页数:9
相关论文
共 26 条
[1]   The intestinal T cell response to α-gliadin in adult celiac disease is focused on a single deamidated glutamine targeted by tissue transglutaminase [J].
Arentz-Hansen, H ;
Körner, R ;
Molberg, O ;
Quarsten, H ;
Vader, W ;
Kooy, YMC ;
Lundin, KEA ;
Koning, F ;
Roepstorff, P ;
Sollid, LM ;
McAdam, SN .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (04) :603-612
[2]   Celiac lesion T cells recognize epitopes that cluster in regions of gliadins rich in proline residues [J].
Arentz-Hansen, H ;
McAdam, SN ;
Molberg, O ;
Fleckenstein, B ;
Lundin, KEA ;
Jorgensen, TJD ;
Jung, G ;
Roepstorff, P ;
Sollid, LM .
GASTROENTEROLOGY, 2002, 123 (03) :803-809
[3]   Gliadin T cell epitope selection by tissue transglutaminase in Celiac disease -: Role of enzyme specificity and pH influence on the transamidation versus deamidation reactions [J].
Fleckenstein, B ;
Molberg, Y ;
Qiao, SW ;
Schmid, DG ;
von der Müllbe, F ;
Elgstoen, K ;
Jung, G ;
Sollid, LM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (37) :34109-34116
[4]   Absence of toxicity of oats in patients with dermatitis herpetiformis [J].
Hardman, CMJ ;
Garioch, JJ ;
Leonard, JN ;
Thomas, HJW ;
Walker, MM ;
Lortan, JE ;
Lister, A ;
Fry, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (26) :1884-1887
[5]   A trial of oats in children with newly diagnosed celiac disease [J].
Hoffenberg, EJ ;
Haas, J ;
Drescher, A ;
Barnhurst, R ;
Osberg, I ;
Bao, F ;
Eisenbarth, G .
JOURNAL OF PEDIATRICS, 2000, 137 (03) :361-366
[6]   Oats to children with newly diagnosed coeliac disease:: a randomised double blind study [J].
Högberg, L ;
Laurin, P ;
Fälth-Magnusson, K ;
Grant, C ;
Grodzinsky, E ;
Jansson, G ;
Ascher, H ;
Browaldh, L ;
Hammersjö, JÅ ;
Lindberg, E ;
Myrdal, U ;
Stenhammar, L .
GUT, 2004, 53 (05) :649-654
[7]   A COMPARISON OF DIETS WITH AND WITHOUT OATS IN ADULTS WITH CELIAC-DISEASE [J].
JANATUINEN, EK ;
PIKKARAINEN, PH ;
KEMPPAINEN, TA ;
KOSMA, VM ;
JARVINEN, RMK ;
UUSITUPA, MIJ ;
JULKUNEN, RJK .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (16) :1033-1037
[8]   No harm from five year ingestion of oats in coeliac disease [J].
Janatuinen, EK ;
Kemppainen, TA ;
Julkunen, RJK ;
Kosma, VM ;
Mäki, M ;
Heikkinen, M ;
Uusitupa, MIJ .
GUT, 2002, 50 (03) :332-335
[9]   Avenin fails to induce a Th1 response in coeliac tissue following in vitro culture [J].
Kilmartin, C ;
Lynch, S ;
Abuzakouk, M ;
Wieser, H ;
Feighery, C .
GUT, 2003, 52 (01) :47-52
[10]   Structural basis for HLA-DQ2-mediated presentation of gluten epitopes in celiac disease [J].
Kim, CY ;
Quarsten, H ;
Bergseng, E ;
Khosla, C ;
Sollid, LM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (12) :4175-4179