生物
FOXP3型
自身免疫
免疫系统
免疫学
Treg细胞
细胞生物学
细胞
T细胞
调节性T细胞
白细胞介素2受体
遗传学
作者
Peter A. Savage,David E J Klawon,Christine H. Miller
出处
期刊:Annual Review of Immunology
[Annual Reviews]
日期:2020-04-26
卷期号:38 (1): 421-453
被引量:140
标识
DOI:10.1146/annurev-immunol-100219-020937
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.
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