Regulatory T Cell Development

被引:197
作者
Savage, Peter A. [1 ]
Klawon, David E. J. [1 ]
Miller, Christine H. [1 ]
机构
[1] Univ Chicago, Dept Pathol, Chicago, IL 60637 USA
来源
ANNUAL REVIEW OF IMMUNOLOGY, VOL 38 | 2020年 / 38卷
关键词
regulatory T cells; Foxp3; thymus; T cell receptor; clonal deletion; antigen; PROMISCUOUS GENE-EXPRESSION; THYMIC EPITHELIAL-CELLS; ANTIGEN-PRESENTING-CELL; MHC CLASS-II; DENDRITIC CELLS; SELF-ANTIGEN; TRANSCRIPTION FACTOR; AUTOIMMUNE-DISEASE; FOXP3; EXPRESSION; TREG CELLS;
D O I
10.1146/annurev-immunol-100219-020937
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Foxp3-expressing CD4(+) regulatory T (Treg) cells play key roles in the prevention of autoimmunity and the maintenance of immune homeostasis and represent a major barrier to the induction of robust antitumor immune responses. Thus, a clear understanding of the mechanisms coordinating Treg cell differentiation is crucial for understanding numerous facets of health and disease and for developing approaches to modulate Treg cells for clinical benefit. Here, we discuss current knowledge of the signals that coordinate Treg cell development, the antigen-presenting cell types that direct Treg cell selection, and the nature of endogenous Treg cell ligands, focusing on evidence from studies in mice. We also highlight recent advances in this area and identify key unanswered questions.
引用
收藏
页码:421 / 453
页数:33
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