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退回寄件人:淋巴细胞迁移机制是原发性硬化性胆管炎的致病因素之一。

Return to sender: Lymphocyte trafficking mechanisms as contributors to primary sclerosing cholangitis.

机构信息

Tytgat Institute for Liver and Intestinal Research, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands; Department of Gastroenterology and Hepatology, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.

Tytgat Institute for Liver and Intestinal Research, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands; Department of Surgery, University of Bonn, Bonn, Germany.

出版信息

J Hepatol. 2019 Sep;71(3):603-615. doi: 10.1016/j.jhep.2019.05.006. Epub 2019 May 18.

Abstract

Primary sclerosing cholangitis (PSC) is an inflammatory disease of the biliary tree, characterised by stricturing bile duct disease and progression to liver fibrosis. The pathophysiology of PSC is still unknown. The concurrence with inflammatory bowel disease (IBD) in about 70% of cases has led to the hypothesis that gut-homing lymphocytes aberrantly traffic to the liver, contributing to disease pathogenesis in patients with both PSC and IBD (PSC-IBD). The discovery of mutual trafficking pathways of lymphocytes to target tissues, and expression of gut-specific adhesion molecules and chemokines in the liver has pointed in this direction. There is now increasing interest in using drugs that intervene with these trafficking pathways (e.g. vedolizumab, etrolizumab) for the treatment of PSC-IBD. In this review we discuss what is currently known about the immunological interactions between the gut and the liver in concomitant PSC and IBD, as well as potential therapeutic options for intervening in these mechanisms.

摘要

原发性硬化性胆管炎(PSC)是一种胆道炎症性疾病,其特征为胆管狭窄和进行性肝纤维化。PSC 的发病机制尚不清楚。约 70%的病例并发炎症性肠病(IBD),这导致了这样一种假说,即肠道归巢淋巴细胞异常迁移到肝脏,导致 PSC 和 IBD(PSC-IBD)患者的疾病发病机制。淋巴细胞向靶组织迁移的共同途径以及肝脏中肠道特异性黏附分子和趋化因子的表达,都指向了这一方向。目前,人们越来越感兴趣的是使用干预这些迁移途径的药物(如vedolizumab、etrolizumab)来治疗 PSC-IBD。在这篇综述中,我们讨论了目前已知的 PSC 和 IBD 同时存在时肠道和肝脏之间的免疫相互作用,以及干预这些机制的潜在治疗选择。

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