| Literature DB >> 32698191 |
Pauline Maisonnasse1, Jérémie Guedj2, Vanessa Contreras1, Sylvie Behillil3,4, Caroline Solas5, Romain Marlin1, Thibaut Naninck1, Andres Pizzorno6, Julien Lemaitre1, Antonio Gonçalves2, Nidhal Kahlaoui1, Olivier Terrier6, Raphael Ho Tsong Fang1, Vincent Enouf3,4,7, Nathalie Dereuddre-Bosquet1, Angela Brisebarre3,4, Franck Touret8, Catherine Chapon1, Bruno Hoen9, Bruno Lina6,10, Manuel Rosa Calatrava6, Sylvie van der Werf3,4, Xavier de Lamballerie8, Roger Le Grand11.
Abstract
Coronavirus disease 2019 (COVID-19) has rapidly become a global pandemic and no antiviral drug or vaccine is yet available for the treatment of this disease1-3. Several clinical studies are ongoing to evaluate the efficacy of repurposed drugs that have demonstrated antiviral efficacy in vitro. Among these candidates, hydroxychloroquine (HCQ) has been given to thousands of individuals infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-the virus that causes COVID-19-worldwide but there is no definitive evidence that HCQ is effective for treating COVID-194-7. Here we evaluated the antiviral activity of HCQ both in vitro and in SARS-CoV-2-infected macaques. HCQ showed antiviral activity in African green monkey kidney cells (Vero E6) but not in a model of reconstituted human airway epithelium. In macaques, we tested different treatment strategies in comparison to a placebo treatment, before and after peak viral load, alone or in combination with azithromycin (AZTH). Neither HCQ nor the combination of HCQ and AZTH showed a significant effect on viral load in any of the analysed tissues. When the drug was used as a pre-exposure prophylaxis treatment, HCQ did not confer protection against infection with SARS-CoV-2. Our findings do not support the use of HCQ, either alone or in combination with AZTH, as an antiviral drug for the treatment of COVID-19 in humans.Entities:
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Year: 2020 PMID: 32698191 DOI: 10.1038/s41586-020-2558-4
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962