Huang Weishan, August Avery
Department of Microbiology and Immunology, Cornell University, Ithaca, New York, USA
J Leukoc Biol. 2015 Mar;97(3):477-85. doi: 10.1189/jlb.1RI0614-293R. Epub 2014 Dec 18.
T cell development, differentiation, and maintenance are orchestrated by 2 key signaling axes: the antigen-specific TCR and cytokine-mediated signals. The TCR signals the recognition of self- and foreign antigens to control T cell homeostasis for immune tolerance and immunity, which is regulated by a variety of cytokines to determine T cell subset homeostasis and differentiation. TCR signaling can synergize with or antagonize cytokine-mediated signaling to fine tune T cell fate; however, the latter is less investigated. Murine models with attenuated TCR signaling strength have revealed that TCR signaling can function as regulatory feedback machinery for T cell homeostasis and differentiation in differential cytokine milieus, such as IL-2-mediated Treg development; IL-7-mediated, naïve CD8(+) T cell homeostasis; and IL-4-induced innate memory CD8(+) T cell development. In this review, we discuss the symphonic cross-talk between TCR and cytokine-mediated responses that differentially control T cell behavior, with a focus on the negative tuning by TCR activation on the cytokine effects.
T细胞的发育、分化和维持由两个关键信号轴协调:抗原特异性TCR和细胞因子介导的信号。TCR发出识别自身和外来抗原的信号,以控制T细胞稳态,实现免疫耐受和免疫,这一过程受多种细胞因子调节,以确定T细胞亚群的稳态和分化。TCR信号可与细胞因子介导的信号协同或拮抗,从而微调T细胞命运;然而,对后者的研究较少。TCR信号强度减弱的小鼠模型表明,TCR信号可作为调节反馈机制,在不同的细胞因子环境中调控T细胞稳态和分化,如IL-2介导的调节性T细胞发育、IL-7介导的初始CD8(+) T细胞稳态以及IL-4诱导的固有记忆CD8(+) T细胞发育。在本综述中,我们讨论了TCR与细胞因子介导的反应之间的协同相互作用,这些反应以不同方式控制T细胞行为,重点关注TCR激活对细胞因子效应的负向调节。