Transcriptional repressor Blimp-1 is essential for T cell homeostasis and self-tolerance

被引:264
作者
Kallies, A [1 ]
Hawkins, ED [1 ]
Belz, GT [1 ]
Metcalf, D [1 ]
Hommel, M [1 ]
Corcoran, LM [1 ]
Hodgkin, PD [1 ]
Nutt, SL [1 ]
机构
[1] Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, Australia
基金
英国惠康基金;
关键词
D O I
10.1038/ni1321
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T cell homeostasis is crucial for a functional immune system, as the accumulation of T cells resulting from lack of regulatory T cells or an inability to shut down immune responses can lead to inflammation and autoimmune pathology. Here we show that Blimp-1, a transcriptional repressor that is a 'master regulator' of terminal B cell differentiation, was expressed in a subset of antigen-experienced CD4(+) and CD8(+) T cells. Mice reconstituted with fetal liver stem cells expressing a mutant Blimp-1 lacking the DNA-binding domain developed a lethal multiorgan inflammatory disease caused by an accumulation of effector and memory T cells. These data identify Blimp-1 as an essential regulator of T cell homeostasis and suggest that Blimp-1 regulates both B cell and T cell differentiation.
引用
收藏
页码:466 / 474
页数:9
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