A role for the terminal C5-C9 complement pathway in idiopathic pulmonary fibrosis

A role for the terminal C5-C9 complement pathway in idiopathic pulmonary fibrosis

Idiopathic pulmonary fibrosis (IPF) is a chronic progressive interstitial lung disease characterized by damage to the alveolar epithelium, leading to fibrosis and excessive accumulation of extracellular matrix in the interstitium of the lung. In the present study we performed high-resolution proteom...

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Bibliographic Details
Main Authors: Liv I. B. Sikkeland, Thor Ueland, May B. Lund, Michael Thomas Durheim, Tom Eirik Mollnes
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-08-01
Series:Frontiers in Medicine
Subjects:
interstitial lung disease
idiopathic pulmonary fibrosis
terminal complement complex
proteomics
bronchial lavage fluid
Online Access:https://www.frontiersin.org/articles/10.3389/fmed.2023.1236495/full

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https://www.frontiersin.org/articles/10.3389/fmed.2023.1236495/full

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