IL-37 is a fundamental inhibitor of innate immunity

被引:726
作者
Nold, Marcel F. [1 ,2 ]
Nold-Petry, Claudia A. [1 ,2 ]
Zepp, Jarod A. [1 ]
Palmer, Brent E. [1 ]
Bufler, Philip [3 ]
Dinarello, Charles A. [1 ]
机构
[1] Univ Colorado Denver, Dept Med, Aurora, CO USA
[2] Monash Univ, Ritchie Ctr, Monash Inst Med Res, Melbourne, Vic 3004, Australia
[3] Univ Munich, Childrens Hosp, D-8000 Munich, Germany
基金
美国国家卫生研究院;
关键词
GROWTH-FACTOR-BETA; DENDRITIC-CELL-FUNCTION; IFN-GAMMA PRODUCTION; RECEPTOR EXPRESSION; TGF-BETA; T-CELLS; BINDING-PROTEIN; IN-VIVO; CYTOKINE; SMAD3;
D O I
10.1038/ni.1944
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The function of interleukin 37 (IL-37; formerly IL-1 family member 7) has remained elusive. Expression of IL-37 in macrophages or epithelial cells almost completely suppressed production of pro-inflammatory cytokines, whereas the abundance of these cytokines increased with silencing of endogenous IL-37 in human blood cells. Anti-inflammatory cytokines were unaffected. Mice with transgenic expression of IL-37 were protected from lipopolysaccharide-induced shock, and showed markedly improved lung and kidney function and reduced liver damage after treatment with lipopolysaccharide. Transgenic mice had lower concentrations of circulating and tissue cytokines (72-95% less) than wild-type mice and showed less dendritic cell activation. IL-37 interacted intracellularly with Smad3 and IL-37-expressing cells and transgenic mice showed less cytokine suppression when endogenous Smad3 was depleted. IL-37 thus emerges as a natural suppressor of innate inflammatory and immune responses.
引用
收藏
页码:1014 / U64
页数:11
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