Department of Immunology, Center for Cancer Immunology Research, The University of Texas-MD Anderson Cancer Center, Houston, Texas, USA.
Nat Med. 2011 Jul 24;17(8):983-8. doi: 10.1038/nm.2426.
Foxp3(+) regulatory T (T(reg)) cells suppress different types of immune responses to help maintain homeostasis in the body. How T(reg) cells regulate humoral immunity, including germinal center reactions, is unclear. Here we identify a subset of T(reg) cells expressing CXCR5 and Bcl-6 that localize to the germinal centers in mice and humans. The expression of CXCR5 on T(reg) cells depends on Bcl-6. These CXCR5(+)Bcl-6(+) T(reg) cells are absent in the thymus but can be generated de novo from CXCR5(-)Foxp3(+) natural T(reg) precursors. A lack of CXCR5(+) T(reg) cells leads to greater germinal center reactions including germinal center B cells, affinity maturation of antibodies and the differentiation of plasma cells. These results unveil a Bcl-6-CXCR5 axis in T(reg) cells that drives the development of follicular regulatory T (T(FR)) cells that function to inhibit the germinal center reactions.
Foxp3(+) 调节性 T(T(reg))细胞抑制不同类型的免疫反应,以帮助维持体内平衡。T(reg)细胞如何调节体液免疫,包括生发中心反应,尚不清楚。在这里,我们鉴定了一群在小鼠和人类生发中心定位于生发中心的表达 CXCR5 和 Bcl-6 的 T(reg)细胞。T(reg)细胞上 CXCR5 的表达依赖于 Bcl-6。这些 CXCR5(+)Bcl-6(+) T(reg)细胞在胸腺中不存在,但可以从 CXCR5(-)Foxp3(+)天然 T(reg)前体中从头生成。缺乏 CXCR5(+)T(reg)细胞会导致更大的生发中心反应,包括生发中心 B 细胞、抗体亲和力成熟和浆细胞分化。这些结果揭示了 T(reg)细胞中的 Bcl-6-CXCR5 轴,该轴驱动滤泡调节性 T(T(FR))细胞的发育,其功能是抑制生发中心反应。