[Research progress of complement system activation involved in idiopathic pulmonary fibrosis].

Y M Liu, Y Y Liang, J Y Zou, N Z Zang, L Yang, L J Pang, X D Lyu
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引用次数: 0

Abstract

Idiopathic pulmonary fibrosis (IPF) is a severe interstitial lung disease, and its pathogenesis remains unclear. In recent years, studies have shown that complement system activation plays an important role in the process of IPF. The inhibition of complement system activation provides a new approach for IPF treatment strategies. This article reviews the recent advances of complement system activation in the molecular mechanisms in the progress of IPF, and the potential therapeutic target in drug development, providing new perspectives for the prevention and treatment of IPF.

[补体系统激活参与特发性肺纤维化的研究进展]。
特发性肺纤维化(IPF)是一种严重的间质性肺疾病,其发病机制尚不清楚。近年来的研究表明,补体系统激活在IPF过程中起着重要作用。抑制补体系统激活为IPF的治疗策略提供了新的途径。本文综述了近年来补体系统激活在IPF分子机制中的研究进展,以及药物开发中潜在的治疗靶点,为IPF的预防和治疗提供新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
3.50
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13832
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