Suppr超能文献

炎症性肠病中的新旧生物制剂和小分子:抗整合素

[Old and New Biologics and Small Molecules in Inflammatory Bowel Disease: Anti Integrins].

作者信息

Kim Kyeong Ok, Lee Si Hyung

机构信息

Department of Internal Medicine, Yeungnam University College of Medicine, Daegu, Korea.

出版信息

Korean J Gastroenterol. 2024 Aug 25;84(2):43-50. doi: 10.4166/kjg.2024.070.

Abstract

Recently, novel biologics or small molecular drugs have been introduced for overcoming the unmet needs associated with anti-tumor necrosis factor α agents for inflammtory bowel disease (IBD) treatment. Among these novel drugs, anti integrin agents block leukocyte trafficking to the intestine by blocking the interaction between integrin and cell adhesion molecules. Vedolizumab (anti-α4β7) is most widely used anti-integrin approved in both ulcerative colitis and Crohn's disease .It has been shown to be effective in both induction and maintenance therapy with a favorable safety profile due to gut selectivity. Several models incorporating clinical, genetic, immune and gut microbial markers to predict response to vedolizumab in IBD have been developed. Etrolizumab (anti-β7) blocks leukocyte trafficking via α4β7 and cell adhesion via αEβ7 integrins. In addition, the introduction of subcutaneous vedolizumab showed similar efficacy and safety with improved patients' convenience. Other investigational anti-integrin therapies include abrilumab (anti-α4β7 IgG2), PN-943 (orally administered and gut-restricted α4β7 antagonist peptide), AJM300 (orally active small molecule inhibitor of α4), and ontamalimab (anti-MAdCAM-1 IgG).

摘要

最近,新型生物制剂或小分子药物被引入,以满足炎症性肠病(IBD)治疗中与抗肿瘤坏死因子α药物相关的未满足需求。在这些新型药物中,抗整合素药物通过阻断整合素与细胞粘附分子之间的相互作用来阻止白细胞向肠道的转运。维多珠单抗(抗α4β7)是在溃疡性结肠炎和克罗恩病中均获批准使用的最广泛的抗整合素药物。由于其肠道选择性,它在诱导和维持治疗中均显示出有效性,且安全性良好。已经开发了几种结合临床、遗传、免疫和肠道微生物标志物来预测IBD患者对维多珠单抗反应的模型。依曲珠单抗(抗β7)通过α4β7阻断白细胞转运,并通过αEβ7整合素阻断细胞粘附。此外,皮下注射维多珠单抗显示出相似的疗效和安全性,同时提高了患者的便利性。其他正在研究的抗整合素疗法包括阿布里单抗(抗α4β7 IgG2)、PN-943(口服且肠道特异性的α4β7拮抗剂肽)、AJM300(α4的口服活性小分子抑制剂)和奥塔马利单抗(抗MAdCAM-1 IgG)。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验