CD4 T cells: fates, functions, and faults

被引:1208
作者
Zhu, Jinfang [1 ]
Paul, William E. [1 ]
机构
[1] NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1182/blood-2008-05-078154
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In 1986, Mosmann and Coff man identified 2 subsets of activated CD4 Tcells, Th1 and Th2 cells, which differed from each other in their pattern of cytokine production and their functions. Our understanding of the importance of the distinct differentiated forms of CD4 T cells and of the mechanisms through which they achieve their differentiated state has greatly expanded over the past 2 decades. Today at least 4 distinct CD4 T-cell subsets have been shown to exist, Th1, Th2, Th17, and iTreg cells. Here we summarize much of what is known about the 4 subsets, including the history of their discovery, their unique cytokine products and related functions, their distinctive expression of cell surface receptors and their characteristic transcription factors, the regulation of their fate determination, and the consequences of their abnormal activation.
引用
收藏
页码:1557 / 1569
页数:13
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