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Dynamic regulation of T follicular regulatory cell responses by interleukin 2 during influenza infection.
Nature Immunology ( IF 27.7 ) Pub Date : 2017-Nov-01 , DOI: 10.1038/ni.3837
Davide Botta , Michael J Fuller , Tatiana T Marquez-Lago , Holly Bachus , John E Bradley , Amy S Weinmann , Allan J Zajac , Troy D Randall , Frances E Lund , Beatriz León , André Ballesteros-Tato

Interleukin 2 (IL-2) promotes Foxp3+ regulatory T (Treg) cell responses, but inhibits T follicular helper (TFH) cell development. However, it is not clear how IL-2 affects T follicular regulatory (TFR) cells, a cell type with properties of both Treg and TFH cells. Using an influenza infection model, we found that high IL-2 concentrations at the peak of the infection prevented TFR cell development by a Blimp-1-dependent mechanism. However, once the immune response resolved, some Treg cells downregulated CD25, upregulated Bcl-6 and differentiated into TFR 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 Treg cells, IL-2 inhibits TFR cell responses.

中文翻译:

流感病毒感染期间白介素2对T滤泡调节细胞反应的动态调节。

白介素2(IL-2)促进Foxp3 +调节性T(T reg)细胞反应,但抑制T卵泡辅助细胞(T FH)的发育。但是,尚不清楚IL-2如何影响T滤泡调节(T FR)细胞,T细胞是具有T reg和T FH细胞特性的细胞类型。使用流感病毒感染模型,我们发现感染高峰期高的IL-2浓度可通过Blimp-1依赖性机制阻止T FR细胞发育。但是,一旦免疫反应消退,一些T reg细胞就会下调CD25,上调Bcl-6并分化为T FR细胞,然后迁移到B细胞滤泡中,以防止自我反应性B细胞克隆的扩增。因此,不同于其对常规T reg细胞的作用,IL-2抑制T FR细胞反应。
更新日期:2017-09-12
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