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The molecular basis of celiac disease.

机译:腹腔疾病的分子基础。

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Celiac disease is caused by inflammatory, gluten specific T cell responses in the small intestine. Invariably such responses are HLA-DQ2 or HLA-DQ8 restricted, providing an explanation for the strong association between celiac disease and these HLA-class II alleles. It is now clear that some native gluten sequences can bind to HLA-DQ2/8 and induce T cell responses. In addition, modification of gluten peptides by the enzyme tissue transglutaminase results in high affinity HLA-DQ2/8 binding peptides that can induce T cell responses. Thus, gluten molecules contain a large number of immunogenic peptides and this is likely to play an important role in the breaking of oral tolerance to gluten.
机译:腹腔疾病是由小肠中的发炎,麸质特异性T细胞反应引起的。此类反应始终受到HLA-DQ2或HLA-DQ8的限制,从而为腹腔疾病与这些HLA-II类等位基因之间的强烈关联提供了解释。现在清楚的是,某些天然麸质序列可以结合HLA-DQ2 / 8并诱导T细胞应答。另外,通过酶组织转谷氨酰胺酶对面筋肽的修饰导致可诱导T细胞反应的高亲和力HLA-DQ2 / 8结合肽。因此,面筋分子包含大量的免疫原性肽,这很可能在破坏口服对面筋的耐受性中起重要作用。

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