IL-35 is elevated in clinical and experimental sepsis and mediates inflammation

被引:44
作者
Cao, Ju [1 ]
Xu, Fang [2 ,3 ]
Lin, Shihui [2 ,3 ]
Tao, Xintong [4 ]
Xiang, Yu [1 ]
Lai, Xiaofei [1 ]
Zhang, Liping [1 ]
机构
[1] Chongqing Med Univ, Affiliated Hosp 1, Dept Lab Med, Chongqing, Peoples R China
[2] Chongqing Med Univ, Affiliated Hosp 1, Dept Emergency, Chongqing 400016, Peoples R China
[3] Chongqing Med Univ, Affiliated Hosp 1, Intens Care Unit, Chongqing 400016, Peoples R China
[4] Chongqing Med Univ, Key Lab Diagnost Med Designated, Minist Educ, Chongqing 400016, Peoples R China
基金
中国国家自然科学基金;
关键词
IL-35; Sepsis; Infection; Inflammation; Immunopathogenesis; REGULATORY T-CELLS; INDUCED IMPAIRMENT; SUPPRESSION; CYTOKINE; TREG; ACTIVATION; MECHANISMS; INDUCTION; EXPRESS; MICE;
D O I
10.1016/j.clim.2015.08.016
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Sepsis carries considerable morbidity and mortality. IL-35 is a newly described cytokine, which plays a regulatory role in infection and immunity. In this study, we found that IL-35 concentration in serum samples from adult or child patients with sepsis was significantly higher compared with that from healthy controls. IL-35 gradually increased according to sepsis severity. Increased serum IL-35 was associated with LOD (Logistic Organ Dysfunction) or SAPS II (Simplified Acute Physiology Score) scores, and correlated with markers of inflammation. In murine abdominal sepsis, administration of anti-IL-35 p35 antibodies significantly diminished dissemination of the bacteria in septic animals, which was accompanied by enhanced local neutrophil recruitment and early increased release of inflammatory cytokines and chemokines. Therefore, sepsis is associated with enhanced release of IL-35. In abdominal sepsis, IL-35 likely facilitates bacterial dissemination. IL-35 plays a major role in the immunopathogenesis of sepsis. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:89 / 95
页数:7
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