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Communications biology · 2022

PIKfyve-specific inhibitors restrict replication of multiple coronaviruses in vitro but not in a murine model of COVID-19.

СтатьяResearch Support, N.I.H., IntramuralПоддержка правительства СШАНазвание и аннотация: Перевод в очереди
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Logue James, Chakraborty Arup R, Johnson Robert, Goyal Girija, Rodas Melissa, Taylor Louis J, Baracco Lauren, McGrath Marisa E, Haupt Robert, Furlong Brooke A, Soong Mercy, Prabhala Pranav, Horvath Viktor, Carlson Kenneth E, Weston Stuart, Ingber Donald E, DePamphilis Melvin L, Frieman Matthew B

Аннотация

The ongoing COVID-19 pandemic has claimed more than 6 million lives and continues to test the world economy and healthcare systems. To combat this pandemic, the biological research community has shifted efforts to the development of medical countermeasures, including vaccines and therapeutics. However, to date, the only small molecules approved for the treatment of COVID-19 in the United States are the nucleoside analogue Remdesivir and the protease inhibitor Paxlovid, though multiple compounds have received Emergency Use Authorization and many more are currently being tested in human efficacy trials. One such compound, Apilimod, is being considered as a COVID-19 therapeutic in a Phase II efficacy trial. However, at the time of writing, there are no published efficacy data in human trials or animal COVID-19 models. Here we show that, while Apilimod and other PIKfyve inhibitors have potent antiviral activity in various cell lines against multiple human coronaviruses, these compounds worsen disease in a COVID-19 murine model when given prophylactically or therapeutically.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты