Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisbon, Portugal.
Blizard Institute, Barts and The London School of Medicine, Queen Mary University of London, London, E1 2AT, United Kingdom.
Trends Immunol. 2017 May;38(5):336-344. doi: 10.1016/j.it.2017.01.007. Epub 2017 Mar 9.
γd T cells have emerged as major sources of the proinflammatory cytokines interleukin-17 (IL-17) and interferon-γ (IFNγ) in multiple models of infection, cancer and autoimmune disease. However, unlike their αβ T cell counterparts that require peripheral activation for effector cell differentiation, γδ T cells instead can be 'developmentally programmed' in the thymus to generate discrete γδ T cell effector subsets with distinctive molecular signatures. Nonetheless, recent studies have presented conflicting viewpoints on the signals involved in thymic γδ T cell development and differentiation, namely on the role of both T cell receptor (TCR)-dependent and TCR-independent factors. Here we review the current data and the ongoing controversies.
γδ T 细胞已成为多种感染、癌症和自身免疫性疾病模型中促炎细胞因子白细胞介素-17(IL-17)和干扰素-γ(IFNγ)的主要来源。然而,与需要外周激活以分化效应细胞的 αβ T 细胞不同,γδ T 细胞可以在胸腺中“发育编程”,以产生具有独特分子特征的离散 γδ T 细胞效应亚群。尽管如此,最近的研究对涉及胸腺 γδ T 细胞发育和分化的信号提出了相互矛盾的观点,即 T 细胞受体(TCR)依赖性和 TCR 非依赖性因素的作用。在这里,我们回顾了当前的数据和正在进行的争论。