Development and function of intestinal innate lymphoid cells

被引:35
作者
Cherrier, M. [1 ,2 ]
Ohnmacht, C. [1 ,2 ]
Cording, S. [1 ,2 ]
Eberl, G. [1 ,2 ]
机构
[1] Inst Pasteur, Dev Lymphoid Tissues Unit, F-75724 Paris, France
[2] CNRS, URA1961, F-75015 Paris, France
关键词
ROR-GAMMA-T; ARYL-HYDROCARBON RECEPTOR; PROINFLAMMATORY IL-17(+); INTERLEUKIN-22; PROTECTS; DIFFERENTIATION; EXPRESSION; FETAL; PROGENITORS; CYTOKINE; ALPHA;
D O I
10.1016/j.coi.2012.03.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Innate lymphoid cells (ILCs) are generated from common lymphoid precursors, like lymphocytes, but do not express an antigen receptor. ILCs include Natural Killer (NK) cells, first described 38 years ago, as well as the more recently discovered lymphoid tissue inducer (LTi) cells, NK22 cells and ILC2s. ILCs reflect many functions of CD4(+) T helper cells by expressing IFN gamma, IL-17, IL-22 or IL-13. However, in contrast to T cells, they are not selected on the basis of antigen specificity, and expand and act shortly after stimulation. Therefore, ILCs play fundamental roles early in responses to infection and injury, in the maintenance of homeostasis, and possibly in the regulation of adaptive immunity. Here, we review the recent data on the development and role of ROR gamma t(+) ILCs and ILC2s in intestinal homeostasis and defense.
引用
收藏
页码:277 / 283
页数:7
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