Laboratory of Experimental Immunology, Immunology Frontier Research Center, Osaka University, Suita, Japan.
Department of Experimental Pathology, Institute for Frontier Medical Sciences, Kyoto University, Kyoto, Japan.
Front Immunol. 2018 Aug 24;9:1910. doi: 10.3389/fimmu.2018.01910. eCollection 2018.
Regulatory T-cells (Treg cells), expressing the transcription factor Foxp3, have an essential role in the control of immune homeostasis. In order to control diverse types of immune responses Treg cells must themselves show functional heterogeneity to control different types of immune responses. Recent advances have made it clear that Treg cells are able to mirror the homing capabilities of known T-helper subtypes such as Th1, Th2, Th17, and T-follicular helper cells (Tfh), allowing them to travel to the sites of inflammation and deliver suppression . One of the more recent discoveries in this category is the description of T-follicular regulatory (Tfr) cells, a specialized subset of Treg cells that control Tfh and resulting antibody responses. In this review we will discuss recent advances in our understanding of Tfr biology and the role of both Tfr and activated extra-follicular Tregs (eTreg) in the control of humoral immunity.
调节性 T 细胞(Treg 细胞)表达转录因子 Foxp3,在控制免疫稳态方面发挥着重要作用。为了控制多种类型的免疫反应,Treg 细胞本身必须表现出功能异质性,以控制不同类型的免疫反应。最近的研究进展表明,Treg 细胞能够模拟已知的 T 辅助细胞亚型(如 Th1、Th2、Th17 和 T 滤泡辅助细胞[Tfh])的归巢能力,使它们能够迁移到炎症部位并进行抑制。在这一领域最近的发现之一是 T 滤泡调节(Tfr)细胞的描述,这是 Treg 细胞的一个特殊亚群,可控制 Tfh 和由此产生的抗体反应。在这篇综述中,我们将讨论我们对 Tfr 生物学的理解以及 Tfr 和激活的滤泡外 Treg(eTreg)在控制体液免疫中的作用的最新进展。