Small intestinal T cells of celiac disease patients recognize a natural pepsin fragment of gliadin

被引:191
作者
van de Wal, Y
Kooy, YMC
van Veelen, PA
Peña, SA
Mearin, LM
Molberg, O
Lundin, KEA
Sollid, LM
Mutis, T
Benckhuijsen, WE
Drijfhout, JW
Koning, F
机构
[1] Leiden Univ, Med Ctr, Dept Immunohaematol, NL-2300 RC Leiden, Netherlands
[2] Leiden Univ, Blood Bank, NL-2300 RC Leiden, Netherlands
[3] Free Univ Amsterdam Hosp, Dept Gastroenterol, NL-1081 HV Amsterdam, Netherlands
[4] Leiden Univ, Med Ctr, Dept Paediat, NL-2300 RC Leiden, Netherlands
[5] Univ Oslo, Rikshosp, Inst Transplantat Immunol, N-0027 Oslo, Norway
关键词
D O I
10.1073/pnas.95.17.10050
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Celiac disease is a common severe intestinal disease resulting from intolerance to dietary wheat gluten and related proteins. The large majority of patients expresses the HLA-DQ2 and/or DQ8 molecules, and gluten-specific HLA-DQ-restricted T cells have been found at the site of the lesion in the gut. The nature of peptides that are recognized by such T cells, however, has been unclear so far. We now report the identification of a gliadin derived epitope that dominantly is recognized by intestinal gluten-specific HLA-DQ8-restricted T cells. The characterization of such epitopes is a key step toward the development of strategies to interfere in mechanisms involved in the pathogenesis of celiac disease.
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收藏
页码:10050 / 10054
页数:5
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