Cutting Edge: CTLA-4 on Effector T Cells Inhibits In Trans

被引:78
|
作者
Corse, Emily
Allison, James P.
机构
[1] Mem Sloan Kettering Canc Ctr, Howard Hughes Med Inst, Dept Immunol, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Ludwig Ctr Canc Immunotherapy, New York, NY 10021 USA
来源
JOURNAL OF IMMUNOLOGY | 2012年 / 189卷 / 03期
基金
美国国家卫生研究院;
关键词
RESPONSES; BLOCKADE; ACTIVATION; EXPRESSION; TOLERANCE; REGULATOR; IMMUNITY; DISEASE; CANCER; MICE;
D O I
10.4049/jimmunol.1200695
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CTLA-4 is thought to inhibit effector T cells both intrinsically, by competing with CD28 for B7 ligands, and extrinsically, through the action of regulatory T cells (Tregs). We studied in vivo responses of normal and CTLA-4-deficient Ag-specific murine effector CD4(+) T cells. We directly demonstrate that effector T cell-restricted CTLA-4 inhibits T cell responses in a cell-extrinsic manner. Cotransfer experiments show that CTLA-4 on normal effector CD4(+) T cells completely abrogates the dramatically increased expansion normally experienced by their CTLA-4-deficient counterparts. Neither the wild-type nor the CTLA-4-deficient T cells express the Treg transcription factor Foxp3 when transferred alone or together. Thus, cell-extrinsic inhibition of T cell responses by CTLA-4 is not limited to Tregs but is also a function of effector T cells. The Journal of Immunology, 2012, 189: 1123-1127.
引用
收藏
页码:1123 / 1127
页数:5
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