| Literature DB >> 33538646 |
Zi-Wei Ye1, Shuofeng Yuan1, Jasper Fuk-Woo Chan1, Anna Jinxia Zhang1, Ching-Yun Yu2, Chon Phin Ong2, Dong Yang1, Chris Chun-Yiu Chan1, Kaiming Tang1, Jianli Cao1, Vincent Kwok-Man Poon1, Chris Chung-Sing Chan1, Jian-Piao Cai1, Hin Chu1, Kwok-Yung Yuen1, Dong-Yan Jin2.
Abstract
Effective treatments for coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are urgently needed. Dexamethasone has been shown to confer survival benefits to certain groups of hospitalized patients, but whether glucocorticoids such as dexamethasone and methylprednisolone should be used together with antivirals to prevent a boost of SARS-CoV-2 replication remains to be determined. Here, we show the beneficial effect of methylprednisolone alone and in combination with remdesivir in the hamster model of SARS-CoV-2 infection. Treatment with methylprednisolone boosted RNA replication of SARS-CoV-2 but suppressed viral induction of proinflammatory cytokines in human monocyte-derived macrophages. Although methylprednisolone monotherapy alleviated body weight loss as well as nasal and pulmonary inflammation, viral loads increased and antibody response against the receptor-binding domain of spike protein attenuated. In contrast, a combination of methylprednisolone with remdesivir not only prevented body weight loss and inflammation, but also dampened viral protein expression and viral loads. In addition, the suppressive effect of methylprednisolone on antibody response was alleviated in the presence of remdesivir. Thus, combinational anti-inflammatory and antiviral therapy might be an effective, safer and more versatile treatment option for COVID-19. These data support testing of the efficacy of a combination of methylprednisolone and remdesivir for the treatment of COVID-19 in randomized controlled clinical trials.Entities:
Keywords: COVID-19; SARS-CoV-2; combination therapy; corticosteroid; remdesivir
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Year: 2021 PMID: 33538646 PMCID: PMC7919885 DOI: 10.1080/22221751.2021.1885998
Source DB: PubMed Journal: Emerg Microbes Infect ISSN: 2222-1751 Impact factor: 7.163