影响 T 滤泡辅助细胞分化和功能的信号。
Signals that influence T follicular helper cell differentiation and function.
机构信息
Cambridge Institute for Medical Research and the Department of Medicine, Addenbrooke's Hospital, Cambridge, CB2 0XY, England, UK.
出版信息
Semin Immunopathol. 2010 Jun;32(2):183-96. doi: 10.1007/s00281-009-0194-z. Epub 2010 Jan 27.
Follicular helper T cells have recently emerged as a separate CD4(+) T helper lineage specialised in provision of help to B cells. They develop independently from Th1, Th2 and Th17 cells and are critical for humoral immunity, including the generation of long-lived and high affinity plasma cells and memory cells crucial for long-term protection against infections. A stepwise differentiation programme has emerged in which T cell receptor (TCR) signalling strength, CD28-mediated costimulation, B cell-derived inducible costimulator ligand signals, induction of c-maf and actions of cytokines, including interleukin (IL)-6 and IL-21, lead to upregulation of the transcriptional repressor B cell lymphoma 6 (Bcl-6) that drives T follicular helper (Tfh) cell differentiation. Bcl-6 turns on a repression programme that targets Blimp-1, transcriptional regulators of other helper lineages and microRNAs. Their concerted actions modulate expression of chemokine receptors, surface molecules and cytokines critical for follicular homing and B cell helper functions. Here, we review the nature of Tfh cells providing help to B cells during the two phases of B cell activation that occur in the outer T zone and, for some B cells, in germinal centres (GC). Recent insights into the signalling events that drive terminal differentiation of Tfh cells critical for selecting somatically mutated GC B cells and the consequences of Tfh dysregulation for immunodeficiency and autoimmune pathology are discussed.
滤泡辅助 T 细胞最近被认为是一种独立的 CD4(+)T 辅助谱系,专门为 B 细胞提供帮助。它们与 Th1、Th2 和 Th17 细胞的发育不同,对体液免疫至关重要,包括产生长寿命和高亲和力的浆细胞和记忆细胞,这对于长期预防感染至关重要。已经出现了一个逐步分化的程序,其中 T 细胞受体 (TCR) 信号强度、CD28 介导的共刺激、B 细胞衍生的可诱导共刺激配体信号、c-maf 的诱导以及细胞因子的作用,包括白细胞介素 (IL)-6 和 IL-21,导致转录抑制剂 B 细胞淋巴瘤 6 (Bcl-6) 的上调,从而驱动 T 滤泡辅助 (Tfh) 细胞分化。Bcl-6 开启了一个抑制程序,该程序针对 Blimp-1、其他辅助谱系的转录调节剂和 microRNAs。它们的协同作用调节了趋化因子受体、表面分子和细胞因子的表达,这些对于滤泡归巢和 B 细胞辅助功能至关重要。在这里,我们回顾了 Tfh 细胞在发生在外周 T 区的 B 细胞激活的两个阶段以及在生发中心 (GC) 中(对于一些 B 细胞)为 B 细胞提供帮助的性质。最近对驱动 Tfh 细胞终末分化的信号事件的深入了解对于选择体细胞突变的 GC B 细胞至关重要,以及 Tfh 失调对免疫缺陷和自身免疫病理的影响也进行了讨论。