Dynamic regulation of T follicular regulatory cell responses by interleukin 2 during influenza infection

被引:184
作者
Botta, Davide [1 ]
Fuller, Michael J. [2 ]
Marquez-Lago, Tatiana T. [3 ,4 ]
Bachus, Holly [2 ]
Bradley, John E. [2 ]
Weinmann, Amy S. [1 ]
Zajac, Allan J. [1 ]
Randall, Troy D. [2 ]
Lund, Frances E. [1 ]
Leon, Beatriz [1 ]
Ballesteros-Tato, Andre [2 ]
机构
[1] Univ Alabama Birmingham, Dept Microbiol, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Med, Div Clin Immunol & Rheumatol, Birmingham, AL 35294 USA
[3] Univ Alabama Birmingham, Informat Inst, Birmingham, AL USA
[4] Univ Alabama Birmingham, Dept Genet, Birmingham, AL USA
基金
美国国家卫生研究院;
关键词
CUTTING EDGE; TGF-BETA; HELPER; STAT5; IL-2; ANTIGEN; DIFFERENTIATION; EXPRESSION; EXPANSION; MICE;
D O I
10.1038/ni.3837
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interleukin 2 (IL-2) promotes Foxp(3+) regulatory T (T-reg) cell responses, but inhibits T follicular helper (T-FH) cell development. However, it is not clear how IL-2 affects T follicular regulatory (T-FR) cells, a cell type with properties of both T-reg 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 T-reg cells downregulated CD25, upregulated Bcl-6 and differentiated into T-FR 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-reg cells, IL-2 inhibits T-FR cell responses.
引用
收藏
页码:1249 / +
页数:18
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