Laboratory of Lymphocyte Signalling and Development, Babraham Institute, Cambridge, United Kingdom.
J Immunol. 2010 Jun 15;184(12):6563-8. doi: 10.4049/jimmunol.1000202.
Th cell functional subsets have unique transcriptional programs that form the molecular basis for T cell differentiation and functions. T follicular helper (TFH) cells have emerged as the main providers of T cell help to B cells during the germinal center (GC) reaction, where B cells undergo selection events through competition for Ag and for access to GC T cell-mediated prosurvival and differentiation signals. Because T cell help is one limiting factor for GC B cells, the molecular mechanisms controlling TFH cell abundance and functionality are central to the GC reaction and generation of long-term humoral immunity. Two signaling pathways are absolutely critical for TFH cells: phosphoinositide-3 kinase pathway and the signaling lymphocyte activation molecule-associated protein. In this review, the molecular mechanisms constituting the signaling network in TFH cells will be explored.
辅助性 T 细胞(Th)功能亚群具有独特的转录程序,为 T 细胞分化和功能形成分子基础。滤泡辅助性 T(TFH)细胞在生发中心(GC)反应中成为 B 细胞 T 细胞辅助的主要提供者,在 GC 反应中,B 细胞通过竞争抗原和获得 GC T 细胞介导的生存和分化信号来进行选择事件。由于 T 细胞辅助是 GC B 细胞的一个限制因素,因此控制 TFH 细胞丰度和功能的分子机制是 GC 反应和产生长期体液免疫的核心。有两条信号通路对 TFH 细胞绝对至关重要:磷酸肌醇 3 激酶途径和信号淋巴细胞激活分子相关蛋白。在这篇综述中,将探讨构成 TFH 细胞信号网络的分子机制。