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减毒编码白细胞介素-19对小鼠结肠炎的改善作用

Amelioration of Murine Colitis by Attenuated Encoding Interleukin-19.

作者信息

Chen Shih-Yao, Chu Chun-Ting, Yang Mei-Lin, Lin Jian-Da, Wang Chung-Teng, Lee Che-Hsin, Lin I-Chen, Shiau Ai-Li, Ling Pin, Wu Chao-Liang

机构信息

Department of Nursing, College of Nursing, Chung Hwa University of Medical Technology, Tainan 71703, Taiwan.

Division of Colorectal Surgery, Department of Surgery, Ditmanson Medical Foundation Chia-Yi Christian Hospital, 539, Zhongxiao Road, Chiayi City 60002, Taiwan.

出版信息

Microorganisms. 2023 Jun 8;11(6):1530. doi: 10.3390/microorganisms11061530.

Abstract

The imbalance of mucosal immunity in the lower gastrointestinal tract can lead to chronic inflammatory bowel diseases (IBDs), including Crohn's disease and ulcerative colitis. IBD is a chronic inflammatory disorder that causes small and/or large intestines ulceration. According to previous studies, recombinant interleukin (IL)-10 protein and genetically modified bacteria secreting IL-10 ameliorate dextran sulfate sodium (DSS)-induced colitis in mice. IL-19 is a transcriptional activator of IL-10 and can alter the balance of T helper 1 (Th)1/Th2 cells in favor of Th2. In this study, we aimed to investigate whether the expression of the murine IL-19 gene carried by () could ameliorate murine IBD. Our results showed that the attenuated could carry and express the IL-19 gene-containing plasmid for IBD gene therapy by reducing the mortality and clinical signs in DSS-induced acute colitis mice as compared to the untreated ones. We also found that IL-10 expression was induced in IL-19-treated colitis mice and prevented inflammatory infiltrates and proinflammatory cytokine expression in these mice. We suggest that encoding IL-19 provides a new strategy for treating IBD in the future.

摘要

下消化道黏膜免疫失衡可导致慢性炎症性肠病(IBD),包括克罗恩病和溃疡性结肠炎。IBD是一种导致小肠和/或大肠溃疡的慢性炎症性疾病。根据以往研究,重组白细胞介素(IL)-10蛋白和分泌IL-10的基因工程菌可改善葡聚糖硫酸钠(DSS)诱导的小鼠结肠炎。IL-19是IL-10的转录激活因子,可改变辅助性T细胞1(Th)1/Th2细胞平衡,使之偏向Th2。在本研究中,我们旨在探究()携带的小鼠IL-19基因的表达是否可改善小鼠IBD。我们的结果显示,与未治疗的小鼠相比,减毒()可通过降低DSS诱导的急性结肠炎小鼠的死亡率和临床症状,来携带并表达含IL-19基因的质粒用于IBD基因治疗。我们还发现,在经IL-19治疗的结肠炎小鼠中可诱导IL-10表达,并可防止这些小鼠出现炎症浸润和促炎细胞因子表达。我们认为,编码IL-19的()为未来治疗IBD提供了一种新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb3c/10304794/646fdf37b4ed/microorganisms-11-01530-g001.jpg

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