肺纤维化形成分子机制研究
Molecular Mechanisms of Pulmonary Fibrosis
DOI: 10.12677/ACM.2018.82017, PDF,   
作者: 冯爱然, 于文成:青岛大学附属医院,山东 青岛
关键词: 肺纤维化炎症氧化应激促凝机制Pulmonary Fibrosis Inflammation Oxidative Stress Coagulation
摘要: 肺纤维化为慢性肺部疾病,特发性肺纤维化(IPF)为其主要类型,也是最严重的纤维化类型,其中位生存期仅为3年。目前肺纤维化发生机制尚不明确,主要研究炎症和免疫学机制、氧化应激和氧化信号通路、促凝机制等领域。本文就三项主要研究领域做一简要综述。
Abstract: Pulmonary fibrosis is a chronic lung disease. Idiopathic pulmonary fibrosis (IPF) is the most common and severe form of the disease, with a median survival of three years. Despite the fact that the precise mechanisms that drive fibrosis in patients remain incompletely understood. Three broad areas have been explored: inflammation and immune mechanisms, oxidative stress and procoagulant mechanisms. This paper gives a brief overview of three major research areas.
文章引用:冯爱然, 于文成. 肺纤维化形成分子机制研究[J]. 临床医学进展, 2018, 8(2): 93-100. https://doi.org/10.12677/ACM.2018.82017

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