Control of Regulatory T Cell Lineage Commitment and Maintenance

被引:459
作者
Josefowicz, Steven Z. [1 ,2 ,3 ]
Rudensky, Alexander [1 ,2 ,3 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Howard Hughes Med Inst, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Program Immunol, New York, NY 10065 USA
[3] Univ Washington, Dept Immunol, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
BETA-MEDIATED INDUCTION; TRANS-RETINOIC ACID; TGF-BETA; FOXP3; EXPRESSION; DIFFERENTIAL REQUIREMENT; STAT5; ACTIVATION; CUTTING EDGE; REG-CELLS; RECEPTOR; CD4(+);
D O I
10.1016/j.immuni.2009.04.009
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 regulatory T (Treg) cells suppress pathology mediated by immune responses against self and foreign antigens and commensal microorganisms. Sustained expression of the transcription factor Foxp3, a key distinguishing feature of Treg cells, is required for their differentiation and suppressor function. In addition, Foxp3 expression prevents deviation of Treg cells into effector T cell lineages and confers dependence of Treg cell survival and expansion on growth factors, foremost interleukin-2, provided by activated effector T cells. In this review we discuss Treg cell differentiation and maintenance with a particular emphasis on molecular regulation of Foxp3 expression, arguably a key to mechanistic understanding of biology of regulatory T cells.
引用
收藏
页码:616 / 625
页数:10
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