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基于证据的溃疡性结肠炎发病机制和治疗:结肠上皮过氧化氢的因果作用。

Evidence-based pathogenesis and treatment of ulcerative colitis: A causal role for colonic epithelial hydrogen peroxide.

机构信息

Disease Pathogenesis, Inflammatory Disease Research Centre, Palm Beach Gardens, FL 33410, United States.

出版信息

World J Gastroenterol. 2022 Aug 21;28(31):4263-4298. doi: 10.3748/wjg.v28.i31.4263.

DOI:10.3748/wjg.v28.i31.4263
PMID:36159014
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9453768/
Abstract

In this comprehensive evidence-based analysis of ulcerative colitis (UC), a causal role is identified for colonic epithelial hydrogen peroxide (HO) in both the pathogenesis and relapse of this debilitating inflammatory bowel disease. Studies have shown that HO production is significantly increased in the non-inflamed colonic epithelium of individuals with UC. HO is a powerful neutrophilic chemotactic agent that can diffuse through colonic epithelial cell membranes creating an interstitial chemotactic molecular "trail" that attracts adjacent intravascular neutrophils into the colonic epithelium leading to mucosal inflammation and UC. A novel therapy aimed at removing the inappropriate HO mediated chemotactic signal has been highly effective in achieving complete histologic resolution of colitis in patients experiencing refractory disease with at least one (biopsy-proven) histologic remission lasting 14 years to date. The evidence implies that therapeutic intervention to prevent the re-establishment of a pathologic HO mediated chemotactic signaling gradient will indefinitely preclude neutrophilic migration into the colonic epithelium constituting a functional cure for this disease. Cumulative data indicate that individuals with UC have normal immune systems and current treatment guidelines calling for the suppression of the immune response based on the belief that UC is caused by an underlying immune dysfunction are not supported by the evidence and may cause serious adverse effects. It is the aim of this paper to present experimental and clinical evidence that identifies HO produced by the colonic epithelium as the causal agent in the pathogenesis of UC. A detailed explanation of a novel therapeutic intervention to normalize colonic HO, its rationale, components, and formulation is also provided.

摘要

在这项关于溃疡性结肠炎 (UC) 的全面循证分析中,结肠上皮细胞产生的过氧化氢 (HO) 在这种使人衰弱的炎症性肠病的发病机制和复发中被确定为因果关系。研究表明,UC 患者的非炎症性结肠上皮中 HO 的产生显著增加。HO 是一种强大的嗜中性粒细胞趋化剂,可扩散穿过结肠上皮细胞膜,在细胞间产生化学趋化分子“轨迹”,吸引相邻血管内的嗜中性粒细胞进入结肠上皮,导致黏膜炎症和 UC。一种旨在消除不适当的 HO 介导的趋化信号的新型疗法,在治疗难治性疾病方面非常有效,可使至少有一次(活检证实)组织学缓解持续 14 年的患者实现结肠炎的完全组织学缓解。这一证据表明,预防病理性 HO 介导的趋化信号梯度重新建立的治疗干预措施将无限期地阻止嗜中性粒细胞向结肠上皮迁移,从而为这种疾病提供功能性治愈。累积数据表明,UC 患者的免疫系统正常,目前基于 UC 是由潜在免疫功能障碍引起的观点而呼吁抑制免疫反应的治疗指南没有得到证据的支持,并且可能会引起严重的不良反应。本文旨在提出实验和临床证据,将结肠上皮产生的 HO 确定为 UC 发病机制中的因果因素。还详细解释了一种使结肠 HO 正常化的新型治疗干预措施的合理性、组成部分和配方。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f9/9453768/ce13d726eca1/WJG-28-4263-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f9/9453768/ea10f3006497/WJG-28-4263-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f9/9453768/a83cac1cee30/WJG-28-4263-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f9/9453768/43c4b7df51ea/WJG-28-4263-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f9/9453768/1e0e3bf0ff03/WJG-28-4263-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f9/9453768/ce13d726eca1/WJG-28-4263-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f9/9453768/ea10f3006497/WJG-28-4263-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f9/9453768/a83cac1cee30/WJG-28-4263-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f9/9453768/43c4b7df51ea/WJG-28-4263-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f9/9453768/1e0e3bf0ff03/WJG-28-4263-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26f9/9453768/ce13d726eca1/WJG-28-4263-g005.jpg

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