Control of Regulatory T Cell Development by the Transcription Factor Foxp3

被引:0
|
作者
Hori, Shohei [1 ]
Nomura, Takashi [2 ]
Sakaguchi, Shimon [1 ,2 ]
机构
[1] Inst Phys & Chem Res, Res Ctr Allergy & Immunol, Immunopathol Lab, Yokohama, Kanagawa 2300045, Japan
[2] Kyoto Univ, Inst Frontier Med Sci, Dept Expt Pathol, Kyoto 6068507, Japan
来源
JOURNAL OF IMMUNOLOGY | 2017年 / 198卷 / 03期
关键词
SELF-TOLERANCE; AUTOIMMUNE-DISEASE; ENTEROPATHY; CD25(+); POLYENDOCRINOPATHY; HOMEOSTASIS; EXPRESSION; INDUCTION; PROTEIN; IPEX;
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Regulatory T cells engage in the maintenance of immunological self-tolerance by actively suppressing self-reactive lymphocytes, Little is known, however, about the molecular mechanism of their development. Here we show that Foxp3, which encodes a transcription factor that is genetically defective in an autoimmune and inflammatory syndrome in humans and mice, is specifically expressed in naturally arising CD4 regulatory T cells. Furthermore, retroviral gene transfer of Foxp3 converts na ve T cells toward a regulatory T cell phenotype similar to that of naturally occurring CD4 regulatory T cells. Thus, Foxp3 is a key regulatory gene for the development of regulatory T cells.
引用
收藏
页码:981 / 985
页数:5
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