Li Yanmei, Wang Yanan, Liu Ying, Wang Yatian, Zuo Xiuli, Li Yanqing, Lu Xuefeng
Department of Gastroenterology, Qilu Hospital, Shandong University, 107 Wenhua West Road, Jinan 250012, China.
Mediators Inflamm. 2014;2014:136329. doi: 10.1155/2014/136329. Epub 2014 Aug 18.
Interleukin- (IL-) 35 and IL-37 are newly discovered immune-suppressing cytokines. They have been described in inflammatory diseases such as collagen-induced arthritis and asthma. However, their expressions in inflammatory bowel disease (IBD) patients have not been yet explored. Our aim was to evaluate serum and inflamed mucosal levels in IBD patients. In 20 ulcerative colitis (UC) patients, 7 Crohn's disease (CD) patients, and 15 healthy subjects, cytokine levels in serum were determined using ELISA and mucosal expression studies were performed by immunohistochemistry, quantitative real-time PCR, and Western blot. The results showed that serums IL-35 and IL-37 levels were significantly decreased in UC and CD patients compared with healthy subjects. The cytokines levels correlated inversely with UC activity. IL-35 was expressed in infiltrating immune cells while IL-37 in intestinal epithelial cells as well as inflammatory cells. IBD patients had significantly higher Ebi3, p35 (two subunits of IL-35), and IL-37b gene expressions; IL-35 and IL-37 protein expressions were higher in IBD patients compared with controls. The study showed that serums IL-35 and IL-37 might be potentially novel biomarkers for IBD. Intestinal IL-35 and IL-37 proteins are upregulated, suggesting that regulating the expression of the two cytokines may provide a new possible target for the treatment of IBD.
白细胞介素-(IL-)35和IL-37是新发现的免疫抑制细胞因子。它们已在诸如胶原诱导性关节炎和哮喘等炎症性疾病中被描述。然而,它们在炎症性肠病(IBD)患者中的表达尚未被研究。我们的目的是评估IBD患者血清和炎症黏膜中的水平。在20例溃疡性结肠炎(UC)患者、7例克罗恩病(CD)患者和15名健康受试者中,使用酶联免疫吸附测定(ELISA)测定血清中的细胞因子水平,并通过免疫组织化学、定量实时聚合酶链反应(PCR)和蛋白质免疫印迹法进行黏膜表达研究。结果显示,与健康受试者相比,UC和CD患者血清中IL-35和IL-37水平显著降低。细胞因子水平与UC活动呈负相关。IL-35在浸润的免疫细胞中表达,而IL-37在肠上皮细胞以及炎症细胞中表达。IBD患者Ebi3、p35(IL-35的两个亚基)和IL-37b基因表达显著更高;与对照组相比,IBD患者中IL-35和IL-37蛋白表达更高。该研究表明,血清IL-35和IL-37可能是IBD潜在的新型生物标志物。肠道中IL-35和IL-37蛋白上调,提示调节这两种细胞因子的表达可能为IBD治疗提供新的可能靶点。