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[解析炎症性肠病的发病机制并寻找新的治疗药物]

[Unraveling the Pathogenesis of Inflammatory Bowel Disease and Search for New Therapeutic Medicines].

作者信息

Hayashi Shusaku

机构信息

Division of Gastrointestinal Pathophysiology, Institute of Natural Medicine, University of Toyama.

出版信息

Yakugaku Zasshi. 2020;140(2):123-128. doi: 10.1248/yakushi.19-00164.

DOI:10.1248/yakushi.19-00164
PMID:32009032
Abstract

The breakdown of the intestinal mucosal barrier has been shown to play a key role in the pathogenesis of intestinal immune-related disorders such as inflammatory bowel disease (IBD). IBD is a chronic inflammatory disorder with intermittent episodes of remission and relapse, and the incidence of IBD in Japan has risen dramatically in recent decades. Although sustained clinical remission has recently been recognized as an important goal of IBD therapy, there are not many treatment options to maintain long-term remission. Intestinal macrophages play pivotal roles in the regulation of immune homeostasis and inflammation in the intestine. Resident intestinal macrophages can regulate themselves and other immune cells, primarily through the spontaneous secretion of interleukin-10 (IL-10). We reported that the enhancement of IL-10 production by intestinal macrophages has the potential to be a novel therapeutic mechanism for maintaining the remission of IBD. Thus, to develop new therapeutic medicines for IBD, we screened the Wakanyaku Library derived from medicinal herbs for the ability to enhance IL-10 production by intestinal macrophages. Some compounds were identified with the potential to enhance IL-10 production by intestinal macrophages and thereby maintain long-term remission in IBD. This review focuses on our recent findings on the role of intestinal macrophages in the pathogenesis of IBD and developing a novel therapeutic strategy aimed at maintaining remission in IBD.

摘要

肠道黏膜屏障的破坏已被证明在肠道免疫相关疾病(如炎症性肠病,IBD)的发病机制中起关键作用。IBD是一种慢性炎症性疾病,有间歇性缓解和复发,近几十年来日本IBD的发病率急剧上升。尽管持续临床缓解最近被认为是IBD治疗的一个重要目标,但维持长期缓解的治疗选择并不多。肠道巨噬细胞在肠道免疫稳态和炎症调节中起关键作用。驻留肠道巨噬细胞主要通过自发分泌白细胞介素-10(IL-10)来调节自身和其他免疫细胞。我们报道肠道巨噬细胞增强IL-10的产生有可能成为维持IBD缓解的一种新的治疗机制。因此,为了开发IBD的新治疗药物,我们筛选了源自草药的和汉药库,以寻找增强肠道巨噬细胞产生IL-10的能力。鉴定出了一些具有增强肠道巨噬细胞产生IL-10从而维持IBD长期缓解潜力的化合物。本综述重点介绍了我们最近关于肠道巨噬细胞在IBD发病机制中的作用以及开发旨在维持IBD缓解的新治疗策略的研究结果。

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[Unraveling the Pathogenesis of Inflammatory Bowel Disease and Search for New Therapeutic Medicines].[解析炎症性肠病的发病机制并寻找新的治疗药物]
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Commun Biol. 2025 Mar 8;8(1):395. doi: 10.1038/s42003-025-07742-4.
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Interleukin-4 Receptor α Subunit Deficiency Alleviates Murine Intestinal Inflammation In Vivo Through the Enhancement of Intestinal Mucosal Barrier Function.白细胞介素-4受体α亚基缺陷通过增强肠道黏膜屏障功能减轻小鼠体内肠道炎症。
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