CD4+CD25+Foxp3+ regulatory T cells induce cytokine deprivation–mediated apoptosis of effector CD4+ T cells

被引:0
作者
Pushpa Pandiyan
Lixin Zheng
Satoru Ishihara
Jennifer Reed
Michael J Lenardo
机构
[1] Laboratory of Immunology,
[2] National Institute of Allergy and Infectious Diseases,undefined
[3] National Institutes of Health,undefined
[4] Laboratory of Cellular and Molecular Immunology,undefined
[5] National Institute of Allergy and Infectious Diseases,undefined
[6] National Institutes of Health,undefined
来源
Nature Immunology | 2007年 / 8卷
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摘要
A key issue in mammalian immunology is how CD4+CD25+Foxp3+ regulatory T cells (Treg 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 γ-chain suppressed Treg cell–induced apoptosis. Treg cell–induced effector CD4+ T cell death required the proapoptotic protein Bim, and effector CD4+ T cells incubated with Treg 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 Treg cells inhibit effector T cell responses.
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页码:1353 / 1362
页数:9
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