Department of Immunology, Duke University Medical Center, Durham, NC, United States.
Front Immunol. 2020 Jan 24;11:42. doi: 10.3389/fimmu.2020.00042. eCollection 2020.
γδ T cells are the first T cell lineage to develop in the thymus and take up residence in a wide variety of tissues where they can provide fast, innate-like sources of effector cytokines for barrier defense. In contrast to conventional αβ T cells that egress the thymus as naïve cells, γδ T cells can be programmed for effector function during development in the thymus. Understanding the molecular mechanisms that determine γδ T cell effector fate is of great interest due to the wide-spread tissue distribution of γδ T cells and their roles in pathogen clearance, immunosurveillance, cancer, and autoimmune diseases. In this review, we will integrate the current understanding of the role of the T cell receptor, environmental signals, and transcription factor networks in controlling mouse innate-like γδ T cell effector commitment.
γδ T 细胞是在胸腺中最先发育并定居于多种组织的 T 细胞谱系,它们可以为屏障防御提供快速的先天效应细胞因子来源。与作为幼稚细胞离开胸腺的常规 αβ T 细胞不同,γδ T 细胞在胸腺发育过程中可以被编程为效应功能。由于 γδ T 细胞在广泛的组织中分布,并且在病原体清除、免疫监视、癌症和自身免疫性疾病中发挥作用,因此了解决定 γδ T 细胞效应命运的分子机制具有重要意义。在这篇综述中,我们将整合目前对 T 细胞受体、环境信号和转录因子网络在控制小鼠先天样 γδ T 细胞效应细胞分化中的作用的理解。