与溃疡性结肠炎深部内镜粘膜愈合相关的粘膜细胞因子表达。

Kazuhiko Uchiyama, Tomohisa Takagi, Katsura Mizushima, Yasuko Hirai, Eiki Murakami, Kohei Asaeda, Mariko Kajiwara-Kubota, Saori Kashiwagi, Yuki Minagawa, Yuma Hotta, Makoto Tanaka, Ken Inoue, Kazuhiro Katada, Kazuhiro Kamada, Takeshi Ishikawa, Hideyuki Konishi, Mitsuo Kishimoto, Yuji Naito, Yoshito Itoh
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引用次数: 0

摘要

背景:溃疡性结肠炎(UC)是一种病因不明的慢性炎症性疾病,目前尚无根治性疗法。细胞因子在 UC 的发病机制中起着重要作用,针对特定细胞因子的疗法已成功治疗了难治性 UC。本研究的目的是测量 UC 中的粘膜细胞因子,并确定哪些细胞因子有助于内镜诊断的非复发性粘膜愈合:这项前瞻性观察研究包括 163 名 UC 患者。方法:这项前瞻性观察研究共纳入了 163 名 UC 患者,在进行内镜检查时通过梅奥内镜评分(MES)和联动彩色成像(LCI)对粘膜进行评估,并通过实时 PCR 对同一部位活检组织中细胞因子 mRNA 的表达进行量化,然后与内镜检查结果进行比较。研究了细胞因子 mRNA 表达与内镜检查结果之间的关系:IFNγ、IL-1β、IL-8、IL-17A 和 IL-23 等细胞因子在 MES 和 LCI 分级的内镜严重程度中的比例显著升高。有趣的是,我们发现根据疾病严重程度,细胞因子(如 IL-22 和 IL-33)的表达在 MES 和 LCI 分级中存在差异。此外,基于 RNA 测序的路径分析比较了被诊断为 MES 0 的 LCI-A 和 LCI-B 患者,发现 IL-5 和 IL-6 参与了内镜粘膜发红的细微差别:本研究首次报道了 UC 黏膜细胞因子表达与黏膜愈合(MH)发病机制之间的相关性,并支持特定细胞因子作为 MH 分子标记物或在 UC MH 发病机制中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mucosal cytokine expression associated with deep endoscopic mucosal healing in ulcerative colitis.

Background: Ulcerative colitis (UC) is a chronic inflammatory disease of unknown cause for which no curative treatments have been developed. Cytokines play an important role in the pathogenesis of UC, and therapies targeting specific cytokines have been successful in treating refractory UC. The purpose of this study was to measure mucosal cytokines in UC and identify those that contribute to non-relapsing mucosal healing diagnosed by endoscopy.

Methods: This prospective, observational study included 163 patients with UC. The mucosa was evaluated by Mayo Endoscopic Subscore (MES) and linked color imaging (LCI) at the time of endoscopy, and cytokine mRNA expression in biopsy tissue taken from the same site was quantified by real-time PCR and compared with endoscopic findings. The relationship between cytokine mRNA expression and endoscopic findings was investigated.

Results: Cytokines such as IFNγ, IL-1β, IL-8, IL-17A, and IL-23 were significantly elevated in proportion to endoscopic severity of MES and LCI classification.Interestingly, we found differences in the expression of cytokines (e.g., IL-22 and IL-33) between MES and LCI classification according to disease severity. Additionally, pathway analysis based on RNA sequencing compared between LCI-A and LCI-B in the patients diagnosed as MES 0 revealed that IL-5 and IL-6 are involved in the finer differences in endoscopic mucosal redness.

Conclusions: This study is the first to report the correlation between mucosal cytokine expression and the pathogenesis of mucosal healing (MH) in UC and supports the contribution of specific cytokines as molecular markers of MH or in the pathogenesis of MH in UC.

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