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NOD2与细菌识别作为克罗恩病的治疗靶点

NOD2 and bacterial recognition as therapeutic targets for Crohn's disease.

作者信息

de Bruyn Magali, Vermeire Séverine

机构信息

a Translational Research in GastroIntestinal Disorders , Department of Chronic Diseases, Metabolism and Ageing (CHROMETA) , KU Leuven , Leuven , Belgium.

b University Hospitals Leuven , Department of Gastroenterology and Hepatology , Leuven , Belgium.

出版信息

Expert Opin Ther Targets. 2017 Dec;21(12):1123-1139. doi: 10.1080/14728222.2017.1397627. Epub 2017 Nov 2.

DOI:10.1080/14728222.2017.1397627
PMID:29096557
Abstract

Crohn's disease (CD) is a chronic, disabling disease of the gastrointestinal tract that mostly affects young adults. Despite extensive research, the pathogenesis of CD is still not completely understood. It is thought that an abnormal mucosal immune response is elicited towards the luminal microbiota in genetically predisposed persons. Genome-wide association studies and meta-analysis have greatly improved our insight into the genetic background of CD. One of the most studied CD-associated genes is nucleotide-binding oligomerization domain 2 (NOD2). Areas covered: We summarize the current knowledge about NOD2, its use in clinical practice, the functional implications of NOD2 mutations and the therapeutic options for targeting NOD2 in CD. Expert opinion: Almost 2 decades after the identification of NOD2 variants in CD, it has become clear that wild type NOD2 is involved in preserving intestinal barrier integrity and immune homeostasis, properly functioning autophagy and balancing the gut microbiota composition. Given the high prevalence and effect size of NOD2 risk alleles in patients with CD and their interplay with important molecular pathways involved in the disease, NOD2 should seriously be considered as a therapeutic target for CD. Several therapeutic approaches exist and these should be further explored to treat NOD2-related deficiencies in CD.

摘要

克罗恩病(CD)是一种慢性致残性胃肠道疾病,主要影响年轻人。尽管进行了广泛研究,但CD的发病机制仍未完全明确。据认为,在具有遗传易感性的个体中,针对管腔微生物群会引发异常的黏膜免疫反应。全基因组关联研究和荟萃分析极大地增进了我们对CD遗传背景的认识。研究最多的与CD相关的基因之一是核苷酸结合寡聚化结构域2(NOD2)。涵盖领域:我们总结了关于NOD2的现有知识、其在临床实践中的应用、NOD2突变的功能影响以及针对CD中NOD2的治疗选择。专家观点:在CD中发现NOD2变异近20年后,已明确野生型NOD2参与维持肠道屏障完整性和免疫稳态、正常发挥自噬功能以及平衡肠道微生物群组成。鉴于NOD2风险等位基因在CD患者中的高患病率和效应大小,以及它们与该疾病中重要分子途径的相互作用,NOD2应被认真视为CD的治疗靶点。存在多种治疗方法,应进一步探索这些方法以治疗CD中与NOD2相关的缺陷。

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