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CD4+ CD25+ Foxp3+ regulatory T cells induce cytokine deprivation -mediated apoptosis of effector CD4+ T cells
被引:909
作者:

Pandiyan, Pushpa
论文数: 0 引用数: 0
h-index: 0
机构: NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA

Zheng, Lixin
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h-index: 0
机构: NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA

Ishihara, Satoru
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h-index: 0
机构: NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA

Reed, Jennifer
论文数: 0 引用数: 0
h-index: 0
机构: NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA

Lenardo, Michael J.
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h-index: 0
机构:
NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA
机构:
[1] NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA
[2] NIAID, Cellular & Mol Immunol Lab, NIH, Bethesda, MD 20892 USA
关键词:
D O I:
10.1038/ni1536
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
A key issue in mammalian immunology is how CD4(+) CD25(+) Foxp3(+) regulatory T cells ( T-reg cells) suppress immune responses. Here we show that Treg cells induced apoptosis of effector CD4+ T cells in vitro and in vivo in a mouse model of inflammatory bowel disease. Treg cells did not affect the early activation or proliferation of effector CD4(+) T cells. Cytokines that signal through the common gamma- chain suppressed T-reg cell- induced apoptosis. T-reg cell-induced effector CD4(+) T cell death required the proapoptotic protein Bim, and effector CD4(+) T cells incubated with T-reg cells showed less activation of the prosurvival kinase Akt and less phosphorylation of the proapoptotic protein Bad. Thus, cytokine deprivation-induced apoptosis is a prominent mechanism by which T-reg cells inhibit effector T cell responses.
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页码:1353 / 1362
页数:10
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