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炎症性肠病的发病机制及生物治疗的最新进展

Pathogenesis of Inflammatory Bowel Disease and Recent Advances in Biologic Therapies.

作者信息

Kim Duk Hwan, Cheon Jae Hee

机构信息

Digestive Disease Center, CHA Bundang Hospital, CHA University, Seongnam 13496, Korea.

Department of Internal Medicine and Institute of Gastroenterology, Yonsei University College of Medicine, Seoul 03722, Korea.; Severance Biomedical Science Institute, Yonsei University College of Medicine, Seoul 03722, Korea.; Brain Korea 21 PLUS Project for Medical Science, Yonsei University College of Medicine, Seoul 03722, Korea.

出版信息

Immune Netw. 2017 Feb;17(1):25-40. doi: 10.4110/in.2017.17.1.25. Epub 2017 Feb 23.

Abstract

Inflammatory bowel disease (IBD) is a chronic intestinal inflammatory disorder with an unknown etiology. IBD is composed of two different disease entities: Crohn's disease (CD) and ulcerative colitis (UC). IBD has been thought to be idiopathic but has two main attributable causes that include genetic and environmental factors. The gastrointestinal tract in which this disease occurs is central to the immune system, and the innate and the adaptive immune systems are balanced in complex interactions with intestinal microbes under homeostatic conditions. However, in IBD, this homeostasis is disrupted and uncontrolled intestinal inflammation is perpetuated. Recently, the pathogenesis of IBD has become better understood owing to advances in genetic and immunologic technology. Moreover, new therapeutic strategies are now being implemented that accurately target the pathogenesis of IBD. Beyond conventional immunesuppressive therapy, the development of biological agents that target specific disease mechanisms has resulted in more frequent and deeper remission in IBD patients, with mucosal healing as a treatment goal of therapy. Future novel biologics should overcome the limitations of current therapies and ensure that individual patients can be treated with optimal drugs that are safe and precisely target IBD.

摘要

炎症性肠病(IBD)是一种病因不明的慢性肠道炎症性疾病。IBD由两种不同的疾病实体组成:克罗恩病(CD)和溃疡性结肠炎(UC)。IBD一直被认为是特发性的,但有两个主要的归因原因,包括遗传和环境因素。发生这种疾病的胃肠道是免疫系统的核心,在稳态条件下,先天免疫系统和适应性免疫系统在与肠道微生物的复杂相互作用中保持平衡。然而,在IBD中,这种稳态被破坏,肠道炎症持续且不受控制。最近,由于遗传和免疫技术的进步,IBD的发病机制已得到更好的理解。此外,现在正在实施新的治疗策略,这些策略准确地针对IBD的发病机制。除了传统的免疫抑制治疗外,针对特定疾病机制的生物制剂的开发已使IBD患者更频繁、更深度地缓解,并将黏膜愈合作为治疗目标。未来的新型生物制剂应克服当前疗法的局限性,并确保个体患者能够使用安全且精确靶向IBD的最佳药物进行治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed1/5334120/1ae707d0b5f8/in-17-25-g001.jpg

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