T-cell and B-cell immunity in celiac disease

被引:60
作者
du Pre, M. Fleur [1 ]
Sollid, Ludvig M.
机构
[1] Univ Oslo, Ctr Immune Regulat, Oslo, Norway
基金
欧洲研究理事会;
关键词
Celiac disease; T cell; B cell; Gluten; Transglutaminase-2; HLA-DQ2; HLA-DQ8; Deamidation; Epitope; Antibody; ANTIGEN-PRESENTING CELLS; SMALL-INTESTINAL MUCOSA; TISSUE TRANSGLUTAMINASE; IN-VIVO; RECOGNIZE GLIADIN; STRUCTURAL BASIS; GLUTEN; EPITOPES; IGA; ANTIBODIES;
D O I
10.1016/j.bpg.2015.04.001
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Celiac disease is an inflammatory disorder with leukocyte infiltration and changes of tissue architecture of the small intestine. The condition develops in genetically susceptible individuals as the result of an inappropriate immune response to gluten proteins of wheat, barley and rye. The clinical manifestations and the histological changes normalize when gluten is eliminated from the diet. CD4(+) T cells that recognize gluten peptides bound to predisposing HLA-DQ molecules play a key role in the pathogenesis. These T cells recognize better gluten peptides that are deamidated, and this posttranslational modification is mediated by the enzyme transglutaminase 2 (TG2). Another hallmark of celiac disease is the production of antibodies to gluten as well as to TG2. A role for B cells in celiac disease pathogenesis is receiving increased recognition. This review will discuss the main discoveries in the field of T-cell and B-cell biology of celiac disease. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:413 / 423
页数:11
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