Pandiyan Pushpa, Zheng Lixin, Ishihara Satoru, Reed Jennifer, Lenardo Michael J
Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.
Nat Immunol. 2007 Dec;8(12):1353-62. doi: 10.1038/ni1536. Epub 2007 Nov 4.
A key issue in mammalian immunology is how CD4+CD25+Foxp3+ regulatory T cells (T(reg) cells) suppress immune responses. Here we show that T(reg) cells induced apoptosis of effector CD4+ T cells in vitro and in vivo in a mouse model of inflammatory bowel disease. T(reg) 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.
哺乳动物免疫学中的一个关键问题是CD4+CD25+Foxp3+调节性T细胞(Treg细胞)如何抑制免疫反应。在此我们表明,在炎症性肠病小鼠模型中,Treg细胞在体外和体内均可诱导效应性CD4+ T细胞凋亡。Treg细胞不影响效应性CD4+ T细胞的早期激活或增殖。通过共同γ链发出信号的细胞因子可抑制Treg细胞诱导的凋亡。Treg细胞诱导的效应性CD4+ T细胞死亡需要促凋亡蛋白Bim,并且与Treg细胞一起孵育的效应性CD4+ T细胞显示存活激酶Akt的激活较少,促凋亡蛋白Bad的磷酸化也较少。因此,细胞因子剥夺诱导的凋亡是Treg细胞抑制效应性T细胞反应的一个突出机制。