CTLA-4 suppresses the pathogenicity of self antigen-specific T cells by cell-intrinsic and cell-extrinsic mechanisms

被引:140
|
作者
Ise, Wataru [1 ,2 ]
Kohyama, Masako [1 ,2 ]
Nutsch, Katherine M. [1 ]
Lee, Hyang Mi [1 ]
Suri, Anish [1 ]
Unanue, Emil R. [1 ]
Murphy, Theresa L. [1 ]
Murphy, Kenneth M. [1 ,2 ]
机构
[1] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63130 USA
[2] Washington Univ, Sch Med, Howard Hughes Med Inst, St Louis, MO 63110 USA
基金
美国国家卫生研究院;
关键词
CUTTING EDGE; IN-VITRO; ACTIVATION; ABSENCE; LYMPHOCYTE; ENGAGEMENT; TOLERANCE; CD28; HOMEOSTASIS; DEFICIENT;
D O I
10.1038/ni.1835
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 inhibitory immunoregulatory receptor CTLA-4 is critical in maintaining self-tolerance, but the mechanisms of its actions have remained controversial. Here we examined the antigen specificity of tissue-infiltrating CD4(+) T cells in Ctla4(-/-) mice. After adoptive transfer, T cells isolated from tissues of Ctla4(-/-) mice showed T cell antigen receptor (TCR)-dependent accumulation in the tissues from which they were derived, which suggested reactivity to tissue-specific antigens. We identified the pancreas-specific enzyme PDIA2 as an autoantigen in Ctla4(-/-) mice. CTLA-4 expressed either on PDIA2-specific effector cells or on regulatory T cells was sufficient to control tissue destruction mediated by PDIA2-specific T cells. Our results demonstrate that both cell-intrinsic and non-cell-autonomous actions of CTLA-4 operate to maintain T cell tolerance to a self antigen.
引用
收藏
页码:129 / U45
页数:8
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