| Literature DB >> 33210491 |
Mengyao Li1, Pan Liu1, Yuehai Ke1, Xue Zhang1.
Abstract
Radiation-induced lung injury (RILI), including acute radiation pneumonitis and chronic radiation-induced pulmonary fibrosis (RIPF), is a side effect of radiotherapy for lung cancer and esophageal cancer. Pulmonary macrophages, as a kind of natural immune cells maintaining lung homeostasis, play a key role in the whole pathological process of RILI. In the early stage of RILI, classically activated M1 macrophages secrete proinflammatory cytokines to induce inflammation and produce massive reactive oxygen species (ROS) through ROS-induced cascade to further impair lung tissue. In the later stage of RILI, alternatively activated M2 macrophages secrete profibrotic cytokines to promote the development of RIPF. The roles of macrophage in the pathogenesis of RILI and the related potential clinical applications are summarized in this review.Entities:
Keywords: Inflammation; Macrophages; Pulmonary fibrosis; Radiation-induced lung injury; Reactive oxygen species; Review
Mesh:
Year: 2020 PMID: 33210491 PMCID: PMC8800789 DOI: 10.3785/j.issn.1008-9292.2020.10.12
Source DB: PubMed Journal: Zhejiang Da Xue Xue Bao Yi Xue Ban ISSN: 1008-9292