Helper T cell differentiation

被引:320
|
作者
Saravia, Jordy [1 ]
Chapman, Nicole M. [1 ]
Chi, Hongbo [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Immunol, 332 N Lauderdale St, Memphis, TN 38105 USA
基金
美国国家卫生研究院;
关键词
T cells; Treg; differentiation; plasticity; immunometabolism; TRANSCRIPTION FACTOR GATA-3; ROR-GAMMA-T; CXC CHEMOKINE RECEPTOR-5; REGULATORY T; TGF-BETA; C-MAF; TH17; CELLS; TH2; T(H)17 CELLS; METABOLIC CHECKPOINT;
D O I
10.1038/s41423-019-0220-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD4(+) T helper cells are key regulators of host health and disease. In the original model, specialized subsets of T helper cells are generated following activation through lineage-specifying cytokines and transcriptional programs, but recent studies have revealed increasing complexities for CD4(+) T-cell differentiation. Here, we first discuss CD4(+) T-cell differentiation from a historical perspective by highlighting the major studies that defined the distinct subsets of T helper cells. We next describe the mechanisms underlying CD4(+) T-cell differentiation, including cytokine-induced signaling and transcriptional networks. We then review current and emerging topics of differentiation, including the plasticity and heterogeneity of T cells, the tissue-specific effects, and the influence of cellular metabolism on cell fate decisions. Importantly, recent advances in cutting-edge approaches, especially systems biology tools, have contributed to new concepts and mechanisms underlying T-cell differentiation and will likely continue to advance this important research area of adaptive immunity.
引用
收藏
页码:634 / 643
页数:10
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