Center of Allergy and Environment (ZAUM), Helmholtz Center and Technical University Munich, Munich, Germany.
Handb Exp Pharmacol. 2022;268:265-296. doi: 10.1007/164_2021_486.
T helper (Th) and regulatory T (Treg) cells represent important effectors of adaptive immunity. They mediate communication between the immune system and tissue sites and thereby coordinate effective defense against environmental threats or maintain tolerance, respectively. Since the discovery of two prototypic T helper cells, Th1 and Th2, additional phenotypic and functional distinct subsets have been described ranging from Th17, Th22, Th9, and T follicular helper cells. The same holds true for regulatory T cells that represent a family with functionally distinct subsets characterized by co-expression of the transcription factors T-bet, Gata3, or RORγt. Here, we summarize the current knowledge on differentiation and function of T helper and regulatory T cell subsets and discuss their lineage stability versus plasticity towards other subsets. In addition, we highlight the direct and indirect contribution of each subset to the pathology of allergies and indicate novel therapies for specific targeting the effector functions of T helper and regulatory T cells.
辅助性 T 细胞(Th)和调节性 T 细胞(Treg)是适应性免疫的重要效应细胞。它们在免疫系统和组织部位之间进行通讯,分别协调有效抵御环境威胁或维持耐受。自发现两种典型的 Th 细胞(Th1 和 Th2)以来,已经描述了其他表型和功能不同的亚群,包括 Th17、Th22、Th9 和滤泡辅助性 T 细胞。调节性 T 细胞也是如此,它们是一个家族,具有功能不同的亚群,其特征是共同表达转录因子 T-bet、Gata3 或 RORγt。在这里,我们总结了关于 Th 和 Treg 细胞亚群的分化和功能的最新知识,并讨论了它们在向其他亚群的分化稳定性与可塑性。此外,我们强调了每个亚群对过敏病理的直接和间接贡献,并指出了针对 Th 和 Treg 细胞效应功能的新型治疗方法。