Tewari Kavita, Nakayama Yumi, Suresh M
Department of Pathobiological Sciences, University of Wisconsin-Madison, Madison, WI 53706, USA.
J Immunol. 2007 Aug 15;179(4):2115-25. doi: 10.4049/jimmunol.179.4.2115.
It is well recognized that IFN-gamma plays a critical role in the control of CD8 T cell expansion and contraction during immune responses to several intracellular pathogens. However, our understanding of the mechanisms underlying the regulation of T cell fate by IFN-gamma is sorely incomplete. Specifically, it is unclear whether regulation of CD8 T cell homeostasis occurs by a T cell intrinsic IFN-gamma pathway. In this study, we have determined the role of the direct effects of IFN-gamma on T cells in regulating the expansion, contraction, and memory phases of the polyclonal CD8 T cell response to an acute viral infection. Using two complementary approaches we demonstrate that the direct effects of IFN-gamma suppress IL-7R expression on Ag-specific effector CD8 T cells, but clonal expansion or deletion of activated CD8 T cells in vivo can occur in the apparent absence of IFN-gammaR signaling in T cells. These findings have clarified fundamental features of control of T cell homeostasis by IFN-gamma in the context of CD8 T cell memory and protective immunity.
众所周知,在对几种细胞内病原体的免疫反应过程中,干扰素-γ在控制CD8 T细胞的扩增和收缩方面起着关键作用。然而,我们对干扰素-γ调节T细胞命运的潜在机制的理解还非常不完整。具体而言,尚不清楚CD8 T细胞稳态的调节是否通过T细胞内在的干扰素-γ途径发生。在本研究中,我们确定了干扰素-γ对T细胞的直接作用在调节多克隆CD8 T细胞对急性病毒感染的反应的扩增、收缩和记忆阶段中的作用。使用两种互补方法,我们证明干扰素-γ的直接作用抑制了抗原特异性效应CD8 T细胞上IL-7R的表达,但在T细胞明显缺乏干扰素-γ受体信号传导的情况下,体内活化的CD8 T细胞的克隆扩增或缺失仍可发生。这些发现阐明了在CD8 T细胞记忆和保护性免疫背景下,干扰素-γ控制T细胞稳态的基本特征。