| Literature DB >> 35914834 |
Yi Luan1, Qianying Yuan1, Qijun Wang1, Susan Compton2, Dianqing Wu3, Wenwen Tang3.
Abstract
Severe acute respiratory syndrome coronavirus 2, responsible for the severe acute respiratory syndrome known as COVID-19, has rapidly spread in almost every country and devastated the global economy and health care system. Lung injury is an early disease manifestation believed to be a major contributor to short- and long-term pathological consequences of COVID-19, and thus drug discovery aiming to ameliorate lung injury could be a potential strategy to treat COVID-19 patients. By inducing a severe acute respiratory syndrome-like pulmonary disease model through infecting A/J mice with murine hepatitis virus strain 1 (MHV-1), we show that i.v. administration of pazopanib ameliorates acute lung injuries without affecting MHV-1 replication. Pazopanib reduces cell apoptosis in MHV-1-infected lungs. Furthermore, we also identified that pazopanib has to be given no later than 48 h after the virus infection without compromising the therapeutic effect. Our study provides a potential treatment for coronavirus-induced lung injuries and support for further evaluation of pazopanib in COVID-19 patients.Entities:
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Year: 2022 PMID: 35914834 PMCID: PMC9378470 DOI: 10.4049/jimmunol.2100968
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.426