Differentiation of Effector CD4 T Cell Populations

被引:2503
作者
Zhu, Jinfang [1 ]
Yamane, Hidehiro [1 ]
Paul, William E. [1 ]
机构
[1] NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA
来源
ANNUAL REVIEW OF IMMUNOLOGY, VOL 28 | 2010年 / 28卷
关键词
CD4 effector T cells; regulatory T cells; T cell differentiation; cytokines; transcription factors; human diseases; FOLLICULAR-HELPER-CELLS; NF-KAPPA-B; TRANSCRIPTION FACTOR FOXP3; IFN-GAMMA PRODUCTION; HYPER-IGE SYNDROME; INTERFERON-REGULATORY FACTOR-4; LOCUS-CONTROL REGION; NONRECEPTOR TYROSINE KINASE; ARYL-HYDROCARBON RECEPTOR; CYTOKINE GENE-EXPRESSION;
D O I
10.1146/annurev-immunol-030409-101212
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 cells play critical roles in mediating adaptive immunity to a variety of pathogens. They are also involved in autoimmunity, asthma, and allergic responses as well as in tumor immunity. During TCR activation in a particular cytokine milieu, naive CD4 T cells may differentiate into one of several lineages of T helper (Th) cells, including Th1, Th2, Th17, and iTreg, as defined by their pattern of cytokine production and function. In this review, we summarize the discovery, functions, and relationships among Th cells; the cytokine and signaling requirements for their development; the networks of transcription factors involved in their differentiation; the epigenetic regulation of their key cytokines and transcription factors; and human diseases involving defective CD4 T cell differentiation.
引用
收藏
页码:445 / 489
页数:45
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