Kabelitz Dieter, Lettau Marcus, Janssen Ottmar
Institute of Immunology, University of Kiel and University Hospital Schleswig-Holstein Campus Kiel, Arnold-Heller-Str. 3, Building 17, D-24105 Kiel, Germany.
F1000Res. 2017 Jun 5;6. doi: 10.12688/f1000research.11057.1. eCollection 2017.
In contrast to conventional T lymphocytes, which carry an αβ T-cell receptor and recognize antigens as peptides presented by major histocompatibility complex class I or class II molecules, human γδ T cells recognize different metabolites such as non-peptidic pyrophosphate molecules that are secreted by microbes or overproduced by tumor cells. Hence, γδ T cells play a role in immunosurveillance of infection and cellular transformation. Until recently, it has been unknown how the γδ T-cell receptor senses such pyrophosphates in the absence of known antigen-presenting molecules. Recent studies from several groups have identified a unique role of butyrophilin (BTN) protein family members in this process, notably of BTN3A1. BTNs are a large family of transmembrane proteins with diverse functions in lipid secretion and innate and adaptive immunity. Here we discuss current models of how BTN molecules regulate γδ T-cell activation. We also address the implications of these recent findings on the design of novel immunotherapeutic strategies based on the activation of γδ T cells.
与携带αβ T细胞受体并将抗原识别为主要组织相容性复合体I类或II类分子呈递的肽的传统T淋巴细胞不同,人类γδ T细胞识别不同的代谢产物,如微生物分泌或肿瘤细胞过量产生的非肽焦磷酸分子。因此,γδ T细胞在感染免疫监视和细胞转化中发挥作用。直到最近,γδ T细胞受体在缺乏已知抗原呈递分子的情况下如何感知此类焦磷酸仍不清楚。几个研究小组最近的研究已经确定了嗜乳脂蛋白(BTN)蛋白家族成员在此过程中的独特作用,特别是BTN3A1。BTN是一大类跨膜蛋白,在脂质分泌以及先天免疫和适应性免疫中具有多种功能。在此,我们讨论BTN分子如何调节γδ T细胞活化的当前模型。我们还探讨了这些最新发现对基于γδ T细胞活化的新型免疫治疗策略设计的影响。