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抗纤维化疗法:我们目前的进展如何?

Antifibrotic Therapies: Where Are We Now?

作者信息

Yoon Young Joon, Friedman Scott L, Lee Youngmin A

机构信息

Division of Liver Diseases, Icahn School of Medicine at Mount Sinai, New York, New York.

出版信息

Semin Liver Dis. 2016 Feb;36(1):87-98. doi: 10.1055/s-0036-1571295. Epub 2016 Feb 12.

Abstract

Fibrosis is the wound-healing response of tissues to injury. Extensive characterization of organ fibrosis mechanisms has identified common core pathways in renal, pulmonary, skin, and liver fibrosis that offer novel antifibrotic approaches across tissues, in addition to organ-specific and/or disease-specific pathways. A growing number of small molecules and biologics have been identified that are reaching clinical trials for one or more fibrotic diseases, making new antifibrotic options for liver fibrosis an emerging reality. The accelerating pace of drug development, which will also include drug repurposing or combination therapies, heightens the need for novel methods for noninvasive fibrosis assessment without liver biopsy, which is critical to establishing surrogate endpoints for patients in clinical trials who have a low risk of hepatic decompensation. In this article the authors review mechanisms of liver fibrosis and outline potential therapeutic targets and antifibrotic therapies in preclinical studies and clinical trials.

摘要

纤维化是组织对损伤的伤口愈合反应。对器官纤维化机制的广泛表征已确定了肾、肺、皮肤和肝纤维化中的共同核心途径,这些途径除了器官特异性和/或疾病特异性途径外,还提供了跨组织的新型抗纤维化方法。越来越多的小分子和生物制剂已被确定正在针对一种或多种纤维化疾病进入临床试验阶段,为肝纤维化带来新的抗纤维化选择已成为现实。药物开发的加速步伐,这也将包括药物重新利用或联合疗法,增加了对无需肝活检的非侵入性纤维化评估新方法的需求,这对于为临床失代偿风险较低的患者在临床试验中建立替代终点至关重要。在本文中,作者回顾了肝纤维化的机制,并概述了临床前研究和临床试验中的潜在治疗靶点和抗纤维化疗法。

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