NKT cells and the regulation of intestinal immunity: a two-way street

被引:32
作者
Brailey, Phillip M. [1 ,2 ]
Lebrusant-Fernandez, Marta [1 ,2 ]
Barral, Patricia [1 ,2 ]
机构
[1] Kings Coll London, Peter Gorer Dept Immunobiol, London, England
[2] Francis Crick Inst, London, England
基金
英国医学研究理事会; 英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
CD1; IBD; lipid antigens; microbiota; NKT cells; KILLER T-CELLS; ALPHA-GALACTOSYLCERAMIDE; ULCERATIVE-COLITIS; MICROBIAL ANTIGENS; ACTIVATION; INNATE; CYTOKINE; INFLAMMATION; RESPONSES; DISTINCT;
D O I
10.1111/febs.15238
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mammalian gastrointestinal compartment is colonised by millions of microorganisms that have a central influence on human health. Intestinal homeostasis requires a continuous dialogue between the commensal bacteria and intestinal immune cells. While interactions between host and commensal bacteria are normally beneficial, allowing training and functional tuning of immune cells, dysregulated immune system-microbiota crosstalk can favour the development of chronic inflammatory diseases, as it is the case for inflammatory bowel disease (IBD). Natural killer T (NKT) cells, which recognise CD1-restricted microbial and self-lipids, contribute to the regulation of mucosal immunity by controlling intestinal homeostasis and participating in the development of IBD. Here, we provide an overview of the recently identified pathways underlying the crosstalk between commensal bacteria and NKT cells and discuss the effect of these interactions in intestinal health and disease.
引用
收藏
页码:1686 / 1699
页数:14
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