Interleukin-38 is elevated in inflammatory bowel diseases and suppresses intestinal inflammation

被引:49
作者
Xie, Cheng [1 ]
Yan, Wei [2 ]
Quan, Runze [1 ]
Chen, Chaoyue [1 ]
Tu, Lei [1 ]
Hou, Xiaohua [1 ]
Fu, Yu [1 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Dept Gastroenterol, Tongji Med Coll, 1277 Jiefang Rd, Wuhan 430022, Hubei, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Hosp, Dept Gastroenterol, Tongji Med Coll, Wuhan 430030, Peoples R China
基金
中国国家自然科学基金;
关键词
Interleukin-38; Inflammatory bowel diseases; Cytokines; GENE-CLUSTER; FAMILY; IL-38; IDENTIFICATION; ASSOCIATION; CYTOKINES; ARTHRITIS; PSORIASIS; MEMBERS;
D O I
10.1016/j.cyto.2019.154963
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There has been no report investigating the role of IL-38 in inflammatory bowel diseases (IBD). Therefore, we investigated the expression of IL-38 in IBD patients and its role in regulating intestinal inflammation. The levels of IL-38 were significantly elevated in the intestine of IBD patients and DSS-induced colitis mice. Immunofluorescence analysis revealed that B cell, not macrophage or T cell, was the source of IL-38 in the intestine. We found that rIL-38 treatment significantly attenuated DSS-induced colitis, including alleviation of weight loss, disease activity index, macroscopic changes and histological damage of colon, along with lower levels of IL-1 beta and TNF-alpha. In vitro, rIL-38 significantly decreased the expression of proinflammatory cytokines in LPS-stimulated RAW 264.7 cells and BMDM. This is the first study suggesting that IL-38 may have a protective effect in IBD, which inhibits the production of proinflammatory cytokines from macrophages. IL-38 may represent a promising therapeutic strategy in IBD.
引用
收藏
页数:10
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