A well adapted regulatory contrivance: regulatory T cell development and the forkhead family transcription factor Foxp3

被引:753
作者
Fontenot, JD [1 ]
Rudensky, AY
机构
[1] Univ Washington, Sch Med, Dept Immunol, Seattle, WA 98195 USA
[2] Univ Washington, Sch Med, Howard Hughes Med Inst, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/ni1179
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The random generation of antigen receptors in developing lymphocytes results in a considerable risk of autoimmunity. Regulatory T cells (T-reg cells) act in a dominant, trans-acting way to actively suppress immune activation and maintain immune tolerance. Here, we discuss the principal advances in our understanding of the molecular mechanisms of T-reg cell development and function with particular emphasis on the forkhead transcription factor Foxp3. Accumulating evidence suggests that T-reg cells represent a dedicated T cell lineage and that Foxp3 functions as the T-reg cell lineage specification factor. The aggressive early- onset lymphoproliferative syndrome resulting from Foxp3 deficiency identifies T-reg cells as vital mediators of immunological tolerance to self and Foxp3 as the mediator of the genetic mechanism of dominant tolerance.
引用
收藏
页码:331 / 337
页数:7
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