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靶向白细胞介素-17作为纤维化疾病的一种新型治疗选择。

Targeting Interleukin-17 as a Novel Treatment Option for Fibrotic Diseases.

作者信息

Sisto Margherita, Lisi Sabrina

机构信息

Department of Translational Biomedicine and Neuroscience (DiBraiN), Section of Human Anatomy and Histology, University of Bari "Aldo Moro", 70124 Bari, Italy.

出版信息

J Clin Med. 2023 Dec 27;13(1):164. doi: 10.3390/jcm13010164.

Abstract

Fibrosis is the end result of persistent inflammatory responses induced by a variety of stimuli, including chronic infections, autoimmune reactions, and tissue injury. Fibrotic diseases affect all vital organs and are characterized by a high rate of morbidity and mortality in the developed world. Until recently, there were no approved antifibrotic therapies. In recent years, high levels of interleukin-17 (IL-17) have been associated with chronic inflammatory diseases with fibrotic complications that culminate in organ failure. In this review, we provide an update on the role of IL-17 in fibrotic diseases, with particular attention to the most recent lines of research in the therapeutic field represented by the epigenetic mechanisms that control IL-17 levels in fibrosis. A better knowledge of the IL-17 signaling pathway implications in fibrosis could design new strategies for therapeutic benefits.

摘要

纤维化是由多种刺激因素引发的持续性炎症反应的最终结果,这些刺激因素包括慢性感染、自身免疫反应和组织损伤。纤维化疾病影响所有重要器官,在发达国家,其发病率和死亡率很高。直到最近,仍没有获批的抗纤维化疗法。近年来,高水平的白细胞介素-17(IL-17)与伴有纤维化并发症并最终导致器官衰竭的慢性炎症性疾病相关。在本综述中,我们提供了关于IL-17在纤维化疾病中作用的最新情况,特别关注以控制纤维化中IL-17水平的表观遗传机制为代表的治疗领域的最新研究方向。更好地了解IL-17信号通路在纤维化中的影响,可为设计新的治疗策略提供依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fa8/10780256/d83246f79fb5/jcm-13-00164-g001.jpg

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