Spatiotemporal regulation of peripheral T cell tolerance

被引:11
|
作者
Brown, Chrysothemis C. [1 ,2 ,3 ]
Rudensky, Alexander Y. [2 ,4 ,5 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Human Oncol & Pathogenesis Program, Immuno Oncol, New York, NY 10065 USA
[2] Weill Cornell Med, Immunol & Microbial Pathogenesis Program, Grad Sch Med Sci, New York, NY 10065 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Pediat, New York, NY 10065 USA
[4] Mem Sloan Kettering Canc Ctr, Howard Hughes Med Inst, New York, NY USA
[5] Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Immunol Program, New York, NY USA
关键词
DENDRITIC CELLS; DIFFERENTIATION; AUTOIMMUNITY; METABOLITES; INDUCTION; ANTIGENS; INHIBITION; IMMUNITY; ABSENCE; LIFE;
D O I
10.1126/science.adg6425
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The incomplete removal of T cells that are reactive against self-proteins during their differentiation in the thymus requires mechanisms of tolerance that prevent their effector function within the periphery. A further challenge is imposed by the need to establish tolerance to the holobiont self, which comprises a highly complex community of commensal microorganisms. Here, we review recent advances in the investigation of peripheral T cell tolerance, focusing on new insights into mechanisms of tolerance to the gut microbiota, including tolerogenic antigen-presenting cell types and immunomodulatory lymphocytes, and their layered ontogeny that underlies developmental windows for establishing intestinal tolerance. While emphasizing the intestine as a model tissue for studying peripheral T cell tolerance, we highlight overlapping and distinct pathways that underlie tolerance to self-antigens versus commensal antigens within a broader framework for immune tolerance.
引用
收藏
页码:472 / 478
页数:7
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