4.7 Review

Virus infection induced pulmonary fibrosis

期刊

JOURNAL OF TRANSLATIONAL MEDICINE
卷 19, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12967-021-03159-9

关键词

Virus infection; Pulmonary fibrosis; Mechanisms; SARS-CoV-2; Potential anti-fibrotic therapy

资金

  1. National High-Level Talents Program
  2. National Natural Science Foundation of China [81770015]
  3. Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program [2017BT01S155]
  4. Open Project of State Key Laboratory of Respiratory Disease [SKLRD-OP-202109]
  5. Special Fund for Science and Technology Innovation of Guangdong Province [2020B1111330001]
  6. Guangzhou Institute of Respiratory Health Open Project (China Evergrande Group)Project [2020GIRHHMS16]

向作者/读者索取更多资源

Pulmonary fibrosis, the end stage of various lung diseases, may be triggered by virus infection, but the specific mechanisms are not fully understood. Studying the relationship between pulmonary fibrosis and various viruses, as well as the infection mechanisms, may provide insights into potential anti-fibrotic treatment targets.
Pulmonary fibrosis is the end stage of a broad range of heterogeneous interstitial lung diseases and more than 200 factors contribute to it. In recent years, the relationship between virus infection and pulmonary fibrosis is getting more and more attention, especially after the outbreak of SARS-CoV-2 in 2019, however, the mechanisms underlying the virus-induced pulmonary fibrosis are not fully understood. Here, we review the relationship between pulmonary fibrosis and several viruses such as Human T-cell leukemia virus (HTLV), Human immunodeficiency virus (HIV), Cytomegalovirus (CMV), Epstein-Barr virus (EBV), Murine gamma-herpesvirus 68 (MHV-68), Influenza virus, Avian influenza virus, Middle East Respiratory Syndrome (MERS)-CoV, Severe acute respiratory syndrome (SARS)-CoV and SARS-CoV-2 as well as the mechanisms underlying the virus infection induced pulmonary fibrosis. This may shed new light on the potential targets for anti-fibrotic therapy to treat pulmonary fibrosis induced by viruses including SARS-CoV-2.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Review Cell Biology

Role of interleukins in the pathogenesis of pulmonary fibrosis

Yi Xin She, Qing Yang Yu, Xiao Xiao Tang

Summary: Interleukins play a crucial role in the development of pulmonary fibrosis, and targeting multiple interleukins with different functions or combining with other therapies may be a future direction. Timing of intervention and understanding the roles of interleukins at different stages are critical for therapeutic strategies.

CELL DEATH DISCOVERY (2021)

Article Cell Biology

Deleterious Role of Th9 Cells in Pulmonary Fibrosis

Kui Miao Deng, Xiang Sheng Yang, Qun Luo, Yi Xin She, Qing Yang Yu, Xiao Xiao Tang

Summary: Th9 cells play a crucial role in the pathogenesis of IPF, promoting pulmonary fibrosis by promoting fibroblast differentiation and Th2 cell development. Neutralizing IL-9 can ameliorate bleomycin-induced pulmonary fibrosis, suggesting Th9-based immunotherapy as a potential treatment strategy.
Article Multidisciplinary Sciences

Multi-omics evaluation of SARS-CoV-2 infected mouse lungs reveals dynamics of host responses

Ni Zhao Wang, Xiang Sheng Yang, Jing Sun, Jin Cun Zhao, Nan Shan Zhong, Xiao Xiao Tang

Summary: This study evaluated the dynamics of lung responses during SARS-CoV-2 infection through transcriptome, proteome, and phosphoproteome analysis of lung tissues from a mouse model. The results showed the fluctuation of host responses and the alternation of signaling pathways and kinases regulating networks at different phases of infection. The study highlighted molecules and signaling pathways that could guide future investigations on COVID-19 therapies.

ISCIENCE (2022)

Article Oncology

Induction of connective tissue growth factor accounts for the inability of glucocorticoid suppression on pulmonary fibrosis

Zhaoni Wang, Xiangsheng Yang, Xin Xu, Qingyang Yu, Yang Peng, Jianxing He, Nanshan Zhong, Xiao Xiao Tang

CLINICAL AND TRANSLATIONAL MEDICINE (2022)

Article Biochemistry & Molecular Biology

Dicoumarol is an effective post-exposure prophylactic for SARS-CoV-2 Omicron infection in human airway epithelium

Yang Peng, Shi-ying Chen, Zhao-ni Wang, Zi-qing Zhou, Jing Sun, Gui-an Zhang, Jia Li, Lei Wang, Jin-cun Zhao, Xiao Xiao Tang, De-Yun Wang, Nan-shan Zhong

Summary: Repurposing existing drugs, such as dicoumarol (DCM), as a potential inhibitor for SARS-CoV-2 infection in airway epithelial cells (AECs) has been found to have potent antiviral activity against Omicron variants. Early treatment of DCM can effectively inhibit Omicron replication in AECs, and the expression of NAD(P)H quinone oxidoreductase 1 (NQO1), a known DCM target, is correlated with disease severity and virus copy levels. DCM treatment disrupts signaling pathways associated with SARS-CoV-2 disease outcomes and can help formulate novel treatment strategies for COVID-19.

SIGNAL TRANSDUCTION AND TARGETED THERAPY (2023)

暂无数据