Commensal-Innate Immune Miscommunication in IBD Pathogenesis

被引:15
|
作者
Cario, Elke [1 ]
机构
[1] Univ Duisburg Essen, Univ Klinikum Essen, Klin Gastroenterol & Hepatol, Div Gastroenterol & Hepatol,Med Sch,Inst Grp 1, DE-45147 Essen, Germany
关键词
Innate immune system; Commensal microbiota; Intestinal mucosa; INFLAMMATORY-BOWEL-DISEASE; INTESTINAL TREFOIL FACTOR; GENOME-WIDE ASSOCIATION; ILEAL CROHNS-DISEASE; EXPERIMENTAL COLITIS; ULCERATIVE-COLITIS; ADAPTIVE IMMUNITY; GENE ATG16L1; COLON-CANCER; SUSCEPTIBILITY;
D O I
10.1159/000338120
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Commensal microbiota plays a key role in the health and disease of the host. The innate immune system comprises an essential functional component of the intestinal mucosal barrier, maintaining hyporesponsiveness to omnipresent harmless commensals in the lumen, but rapidly recognizing and combating invading bacteria through diverse antimicrobial mechanisms. Interactions between commensals and innate immune cells are constant, multidimensional and entirely context-dependent. Environment, genetics and host defense differentially modulate commensal-innate immune effects and functions in the intestinal mucosa. In IBD, dysbiosis, mucus layer disruption, impairment in bacterial clearance, intestinal epithelial cell barrier dysfunction and/or immune cell deregulation may lead to commensal-innate immune miscommunication, which critically drives mucosal inflammation and associated cancer. Copyright (C) 2012 S. Karger AG, Basel
引用
收藏
页码:334 / 340
页数:7
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