Department of Immunology, Garvan Institute of Medical Research, 384 Victoria Street, Darlinghurst, New South Wales 2010, Australia.
Department of Medicine, St Vincent's Clinical School, University of NSW, Sydney, New South Wales 2010, Australia.
Nat Commun. 2017 Mar 17;8:14647. doi: 10.1038/ncomms14647.
T follicular regulatory (Tfr) cells control the magnitude and specificity of the germinal centre reaction, but how regulation is contained to ensure generation of high-affinity antibody is unknown. Here we show that this balance is maintained by the reciprocal influence of interleukin (IL)-2 and IL-21. The number of IL-2-dependent FoxP3 regulatory T cells is increased in the peripheral blood of human patients with loss-of-function mutations in the IL-21 receptor (IL-21R). In mice, IL-21:IL-21R interactions influence the phenotype of T follicular cells, reducing the expression of CXCR4 and inhibiting the expansion of Tfr cells after T-cell-dependent immunization. The negative effect of IL-21 on Tfr cells in mice is cell intrinsic and associated with decreased expression of the high affinity IL-2 receptor (CD25). Bcl-6, expressed in abundance in Tfr cells, inhibits CD25 expression and IL-21-mediated inhibition of CD25 is Bcl-6 dependent. These findings identify a mechanism by which IL-21 reinforces humoral immunity by restricting Tfr cell proliferation.
滤泡辅助性 T 细胞(Tfh)调节细胞控制生发中心反应的幅度和特异性,但调控如何被限制以确保产生高亲和力的抗体尚不清楚。本文中,我们发现这种平衡通过白细胞介素(IL)-2 和 IL-21 的相互影响来维持。在 IL-21 受体(IL-21R)功能丧失突变的人类患者的外周血中,IL-2 依赖性 FoxP3 调节性 T 细胞数量增加。在小鼠中,IL-21:IL-21R 相互作用影响滤泡辅助性 T 细胞的表型,减少 CXCR4 的表达,并抑制 T 细胞依赖性免疫后 Tfr 细胞的扩增。IL-21 对小鼠 Tfr 细胞的负向作用是细胞内的,与高亲和力 IL-2 受体(CD25)的表达降低有关。大量表达于 Tfr 细胞中的 Bcl-6 抑制 CD25 的表达,而 IL-21 介导的 CD25 抑制依赖于 Bcl-6。这些发现确定了一种机制,即 IL-21 通过限制 Tfr 细胞增殖来增强体液免疫。