Botta Davide, Fuller Michael J, Marquez-Lago Tatiana T, Bachus Holly, Bradley John E, Weinmann Amy S, Zajac Allan J, Randall Troy D, Lund Frances E, León Beatriz, Ballesteros-Tato André
Department of Microbiology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Department of Medicine, Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Alabama, USA.
Nat Immunol. 2017 Nov;18(11):1249-1260. doi: 10.1038/ni.3837. Epub 2017 Sep 11.
Interleukin 2 (IL-2) promotes Foxp3 regulatory T (T) cell responses, but inhibits T follicular helper (T) cell development. However, it is not clear how IL-2 affects T follicular regulatory (T) cells, a cell type with properties of both T and T cells. Using an influenza infection model, we found that high IL-2 concentrations at the peak of the infection prevented T cell development by a Blimp-1-dependent mechanism. However, once the immune response resolved, some T cells downregulated CD25, upregulated Bcl-6 and differentiated into T cells, which then migrated into the B cell follicles to prevent the expansion of self-reactive B cell clones. Thus, unlike its effects on conventional T cells, IL-2 inhibits T cell responses.
白细胞介素2(IL-2)可促进叉头框蛋白3调节性T(Treg)细胞反应,但会抑制滤泡辅助性T(Tfh)细胞发育。然而,目前尚不清楚IL-2如何影响滤泡调节性T(Tfr)细胞,这是一种兼具Treg和Tfh细胞特性的细胞类型。利用流感感染模型,我们发现感染高峰期的高浓度IL-2通过一种依赖于B淋巴细胞诱导成熟蛋白1(Blimp-1)的机制阻止了Tfr细胞的发育。然而,一旦免疫反应消退,一些Tfr细胞下调CD25,上调B细胞淋巴瘤因子6(Bcl-6)并分化为Tfr细胞,然后迁移到B细胞滤泡中以阻止自身反应性B细胞克隆的扩增。因此,与它对传统T细胞的作用不同,IL-2会抑制Tfr细胞反应。