Department of Immunobiology, Yale School of Medicine, New Haven, CT, United States.
Department of Internal Medicine, Yale School of Medicine, New Haven, CT, United States.
Front Immunol. 2021 Jun 10;12:679909. doi: 10.3389/fimmu.2021.679909. eCollection 2021.
T follicular regulatory cells, or Tfr cells, are a discernable population of regulatory T (Treg) cells that migrate to the B cell follicle and germinal center (GC) upon immune challenge. These cells express the transcription factor Bcl6, the master regulator required for development and differentiation of T follicular helper cells, and are among a group of previously described Treg cells that use T helper cell-associated transcription factors to adapt their regulatory function to diverse milieus for maintenance of immune homeostasis. While there is consensus that Tfr cells control B-cell autoreactivity, it has been unclear whether they regulate productive, antigen-specific GC responses. Accordingly, understanding the regulatory balancing that Tfr cells play in maintenance of B-cell tolerance while optimizing productive humoral immunity is crucial for vaccine-design strategies. To this end, we discuss recent evidence that Tfr cells promote humoral immunity and memory following viral infections, fitting with the accepted role of Treg cells in maintaining homeostasis with promotion of productive immunity, while mitigating that which is potentially pathological. We also propose models in which Tfr cells regulate antigen-specific B cell responses.
T 滤泡调节细胞(Tfr 细胞)是一类可识别的调节性 T(Treg)细胞群,在免疫挑战时迁移到 B 细胞滤泡和生发中心(GC)。这些细胞表达转录因子 Bcl6,是 T 滤泡辅助细胞发育和分化所必需的主调控因子,属于先前描述的 Treg 细胞群的一部分,这些细胞使用辅助性 T 细胞相关转录因子来适应其调节功能,以维持免疫稳态的多样化环境。虽然人们普遍认为 Tfr 细胞控制 B 细胞自身反应,但尚不清楚它们是否调节有产性、抗原特异性 GC 反应。因此,了解 Tfr 细胞在维持 B 细胞耐受的同时优化有产性体液免疫中所发挥的调节平衡作用,对于疫苗设计策略至关重要。为此,我们讨论了最近的证据,表明 Tfr 细胞在病毒感染后促进体液免疫和记忆,这与 Treg 细胞在维持稳态和促进有产性免疫的同时减轻潜在病理性免疫的公认作用一致。我们还提出了 Tfr 细胞调节抗原特异性 B 细胞反应的模型。