Dantzler Kathleen W, de la Parte Lauren, Jagannathan Prasanna
Department of Medicine Stanford University Stanford CA USA.
Clin Transl Immunology. 2019 Aug 28;8(8):e1072. doi: 10.1002/cti2.1072. eCollection 2019.
γδ T cells are fascinating cells that bridge the innate and adaptive immune systems. They have long been known to proliferate rapidly following infection; however, the identity of the specific γδ T cell subsets proliferating and the role of this expansion in protection from disease have only been explored more recently. Several recent studies have investigated γδ T-cell responses to vaccines targeting infections such as , and influenza, and studies in animal models have provided further insight into the association of these responses with improved clinical outcomes. In this review, we examine the evidence for a role for γδ T cells in vaccine-induced protection against various bacterial, protozoan and viral infections. We further discuss results suggesting potential mechanisms for protection, including cytokine-mediated direct and indirect killing of infected cells, and highlight remaining open questions in the field. Finally, building on current efforts to integrate strategies targeting γδ T cells into immunotherapies for cancer, we discuss potential approaches to improve vaccines for infectious diseases by inducing γδ T-cell activation and cytotoxicity.
γδ T细胞是连接固有免疫系统和适应性免疫系统的迷人细胞。长期以来,人们已知它们在感染后会迅速增殖;然而,增殖的特定γδ T细胞亚群的身份以及这种扩增在预防疾病中的作用直到最近才得到更多探索。最近的几项研究调查了γδ T细胞对针对诸如[此处原文缺失具体感染名称]、[此处原文缺失具体感染名称]和流感等感染的疫苗的反应,并且在动物模型中的研究进一步深入了解了这些反应与改善临床结果之间的关联。在这篇综述中,我们研究了γδ T细胞在疫苗诱导的针对各种细菌、原生动物和病毒感染的保护作用方面的证据。我们进一步讨论了表明潜在保护机制的结果,包括细胞因子介导的对感染细胞的直接和间接杀伤,并强调了该领域中仍然存在的未解决问题。最后,基于目前将针对γδ T细胞的策略整合到癌症免疫治疗中的努力,我们讨论了通过诱导γδ T细胞活化和细胞毒性来改进传染病疫苗的潜在方法。