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炎症性肠病黏膜愈合及治疗的新靶点。

New targets for mucosal healing and therapy in inflammatory bowel diseases.

机构信息

Medical Clinic 1, Friedrich-Alexander University Clinic, University of Erlangen-Nürnberg, Erlangen, Germany.

出版信息

Mucosal Immunol. 2014 Jan;7(1):6-19. doi: 10.1038/mi.2013.73. Epub 2013 Oct 2.

Abstract

Healing of the inflamed mucosa (mucosal healing) is an emerging new goal for therapy and predicts clinical remission and resection-free survival in inflammatory bowel diseases (IBDs). The era of antitumor necrosis factor (TNF) antibody therapy was a remarkable progress in IBD therapy and anti-TNF agents led to mucosal healing in a subgroup of IBD patients; however, many patients do not respond to anti-TNF treatment highlighting the relevance of finding new targets for therapy of IBD. In particular, current studies are addressing the role of other anticytokine agents including antibodies against interleukin (IL)-6R, IL-13, and IL-12/IL-23 as well as new anti-inflammatory concepts (regulatory T cell therapy, Smad7 antisense, Jak inhibition, Toll-like receptor 9 stimulation, worm eggs). In addition, blockade of T-cell homing via the integrins α4β7 and the addressin mucosal vascular addressin cell adhesion molecule 1 (MAdCAM-1) emerges as a promising new approach for IBD therapy. Here, new approaches for achieving mucosal healing are discussed as well as their implications for future therapy of IBD.

摘要

炎症黏膜的愈合(黏膜愈合)是治疗的新兴新目标,可预测炎症性肠病(IBD)的临床缓解和无切除生存。抗肿瘤坏死因子(TNF)抗体治疗的时代是 IBD 治疗的显著进展,抗 TNF 药物使 IBD 患者亚组的黏膜愈合;然而,许多患者对抗 TNF 治疗无反应,突出了寻找 IBD 治疗新靶点的相关性。特别是,目前的研究正在探讨其他抗细胞因子药物的作用,包括针对白细胞介素(IL)-6R、IL-13 和 IL-12/IL-23 的抗体以及新的抗炎概念(调节性 T 细胞治疗、Smad7 反义寡核苷酸、Jak 抑制、Toll 样受体 9 刺激、蠕虫卵)。此外,通过整合素 α4β7 和黏膜血管地址素细胞黏附分子 1(MAdCAM-1)阻断 T 细胞归巢,为 IBD 治疗提供了一种很有前途的新方法。在此,讨论了实现黏膜愈合的新方法及其对 IBD 未来治疗的影响。

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