Phenotypical and functional specialization of FOXP3+ regulatory T cells

被引:621
作者
Campbell, Daniel J. [1 ,2 ]
Koch, Meghan A. [1 ,2 ]
机构
[1] Benaroya Res Inst, Program Immunol, Seattle, WA 98103 USA
[2] Univ Washington, Dept Immunol, Sch Med, Seattle, WA 98195 USA
关键词
TRANSCRIPTION FACTOR; CUTTING EDGE; DENDRITIC CELLS; TH17; CELLS; TGF-BETA; 1,25-DIHYDROXYVITAMIN D-3; RHEUMATOID-ARTHRITIS; SUPPRESSIVE ACTIVITY; LYMPH-NODES; L-SELECTIN;
D O I
10.1038/nri2916
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Forkhead box P3 (FOXP3)(+) regulatory T (T-Reg) cells prevent autoimmune disease, maintain immune homeostasis and modulate immune responses during infection. To accomplish these tasks, T-Reg cell activity is precisely controlled, and this requires T-Reg cells to alter their migratory, functional and homeostatic properties in response to specific cues in the immune environment. We review progress in understanding the diversity of T-Reg cells, T-Reg cell function in different anatomical and inflammatory settings, and the influence of the immune environment on T-Reg cell activity. We also consider how these factors affect immune-mediated disease in the contexts of infection, autoimmunity, cancer and transplantation.
引用
收藏
页码:119 / 130
页数:12
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