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维多珠单抗诱发的新发肠外表现

Vedolizumab-Induced De Novo Extraintestinal Manifestations.

作者信息

Diaz Liege I, Keihanian Tara, Schwartz Ingrid, Bin Kim Su, Calmet Fernando, Alejandra Quintero Maria, Abreu Maria T

机构信息

Dr Diaz is an advanced gastroenterology fellow in the Department of Gastrointestinal Oncology at the Moffitt Cancer Center in Tampa, Florida.

Dr Keihanian is a gastroenterology fellow in the Department of Internal Medicine in the Division of Gastroenterology at the University of Miami Miller School of Medicine in Miami, Florida.

出版信息

Gastroenterol Hepatol (N Y). 2020 Feb;16(2):75-81.

Abstract

Vedolizumab is an α4β7 integrin antagonist with gut-specific effects on lymphocyte and monocyte trafficking. Although the treatment is beneficial for inflammatory bowel disease (IBD), the effects of vedolizumab on extraintestinal manifestations (EIMs) have not been well described. The gut-specific effects of the medication may have diverse outcomes on EIMs. We hypothesize that EIMs may be unmasked by systemic availability of gut-homing effector cells. The goal of this study is to describe de novo EIMs of IBD patients who were started on vedolizumab. A retrospective chart review of 71 patients from January 2011 to October 2017, including clinical and medication history and colonoscopy results, was performed. EIMs occurred in 26.7% of patients who were started on vedolizumab. The most common EIMs were arthralgias, perianal fistula, and pyoderma gangrenosum. There was a trend toward a greater occurrence of EIMs in patients with Crohn's disease compared to ulcerative colitis. Our retrospective study suggests that inhibition of gut-specific effector cells results in activated lymphocytes and/or monocytes that cause inflammation in other tissues. More studies are needed to confirm these observations and to develop biomarkers that predict patients at risk for EIMs and perianal fistulas while on vedolizumab.

摘要

维多珠单抗是一种α4β7整合素拮抗剂,对淋巴细胞和单核细胞的迁移具有肠道特异性作用。尽管该治疗对炎症性肠病(IBD)有益,但维多珠单抗对肠外表现(EIMs)的影响尚未得到充分描述。该药物的肠道特异性作用可能对EIMs产生不同的结果。我们假设EIMs可能会因肠道归巢效应细胞的全身可用性而显现出来。本研究的目的是描述开始使用维多珠单抗的IBD患者的新发EIMs。对2011年1月至2017年10月期间的71例患者进行了回顾性病历审查,包括临床和用药史以及结肠镜检查结果。开始使用维多珠单抗的患者中,26.7%出现了EIMs。最常见的EIMs是关节痛、肛周瘘和坏疽性脓皮病。与溃疡性结肠炎相比,克罗恩病患者中EIMs的发生率有更高的趋势。我们的回顾性研究表明,抑制肠道特异性效应细胞会导致活化的淋巴细胞和/或单核细胞,从而在其他组织中引发炎症。需要更多的研究来证实这些观察结果,并开发生物标志物来预测使用维多珠单抗时发生EIMs和肛周瘘的风险患者。

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