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Lack of antiviral activity of darunavir against SARS-CoV-2

OBJECTIVES: Given the high need and the absence of specific antivirals for treatment of COVID-19 (the disease caused by severe acute respiratory syndrome-associated coronavirus-2 [SARS-CoV-2]), human immunodeficiency virus (HIV) protease inhibitors are being considered as therapeutic alternatives. M...

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Autores principales: De Meyer, Sandra, Bojkova, Denisa, Cinatl, Jindrich, Van Damme, Ellen, Buyck, Christophe, Van Loock, Marnix, Woodfall, Brian, Ciesek, Sandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7258847/
https://www.ncbi.nlm.nih.gov/pubmed/32479865
http://dx.doi.org/10.1016/j.ijid.2020.05.085
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author De Meyer, Sandra
Bojkova, Denisa
Cinatl, Jindrich
Van Damme, Ellen
Buyck, Christophe
Van Loock, Marnix
Woodfall, Brian
Ciesek, Sandra
author_facet De Meyer, Sandra
Bojkova, Denisa
Cinatl, Jindrich
Van Damme, Ellen
Buyck, Christophe
Van Loock, Marnix
Woodfall, Brian
Ciesek, Sandra
author_sort De Meyer, Sandra
collection PubMed
description OBJECTIVES: Given the high need and the absence of specific antivirals for treatment of COVID-19 (the disease caused by severe acute respiratory syndrome-associated coronavirus-2 [SARS-CoV-2]), human immunodeficiency virus (HIV) protease inhibitors are being considered as therapeutic alternatives. METHODS: Prezcobix/Rezolsta is a fixed-dose combination of 800 mg of the HIV protease inhibitor darunavir (DRV) and 150 mg cobicistat, a CYP3A4 inhibitor, which is indicated in combination with other antiretroviral agents for the treatment of HIV infection. There are currently no definitive data on the safety and efficacy of DRV/cobicistat for the treatment of COVID-19. The in vitro antiviral activity of darunavir against a clinical isolate from a patient infected with SARS-CoV-2 was assessed. RESULTS: DRV showed no antiviral activity against SARS-CoV-2 at clinically relevant concentrations (EC(50) > 100 μM). Remdesivir, used as a positive control, demonstrated potent antiviral activity (EC(50) = 0.38 μM). CONCLUSIONS: Overall, the data do not support the use of DRV for the treatment of COVID-19.
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spelling pubmed-72588472020-05-29 Lack of antiviral activity of darunavir against SARS-CoV-2 De Meyer, Sandra Bojkova, Denisa Cinatl, Jindrich Van Damme, Ellen Buyck, Christophe Van Loock, Marnix Woodfall, Brian Ciesek, Sandra Int J Infect Dis Article OBJECTIVES: Given the high need and the absence of specific antivirals for treatment of COVID-19 (the disease caused by severe acute respiratory syndrome-associated coronavirus-2 [SARS-CoV-2]), human immunodeficiency virus (HIV) protease inhibitors are being considered as therapeutic alternatives. METHODS: Prezcobix/Rezolsta is a fixed-dose combination of 800 mg of the HIV protease inhibitor darunavir (DRV) and 150 mg cobicistat, a CYP3A4 inhibitor, which is indicated in combination with other antiretroviral agents for the treatment of HIV infection. There are currently no definitive data on the safety and efficacy of DRV/cobicistat for the treatment of COVID-19. The in vitro antiviral activity of darunavir against a clinical isolate from a patient infected with SARS-CoV-2 was assessed. RESULTS: DRV showed no antiviral activity against SARS-CoV-2 at clinically relevant concentrations (EC(50) > 100 μM). Remdesivir, used as a positive control, demonstrated potent antiviral activity (EC(50) = 0.38 μM). CONCLUSIONS: Overall, the data do not support the use of DRV for the treatment of COVID-19. Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. 2020-08 2020-05-29 /pmc/articles/PMC7258847/ /pubmed/32479865 http://dx.doi.org/10.1016/j.ijid.2020.05.085 Text en © 2020 Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
De Meyer, Sandra
Bojkova, Denisa
Cinatl, Jindrich
Van Damme, Ellen
Buyck, Christophe
Van Loock, Marnix
Woodfall, Brian
Ciesek, Sandra
Lack of antiviral activity of darunavir against SARS-CoV-2
title Lack of antiviral activity of darunavir against SARS-CoV-2
title_full Lack of antiviral activity of darunavir against SARS-CoV-2
title_fullStr Lack of antiviral activity of darunavir against SARS-CoV-2
title_full_unstemmed Lack of antiviral activity of darunavir against SARS-CoV-2
title_short Lack of antiviral activity of darunavir against SARS-CoV-2
title_sort lack of antiviral activity of darunavir against sars-cov-2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7258847/
https://www.ncbi.nlm.nih.gov/pubmed/32479865
http://dx.doi.org/10.1016/j.ijid.2020.05.085
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