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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier Ltd on behalf of International Society for Infectious Diseases.
2020
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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. |
format | Online Article Text |
id | pubmed-7258847 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. |
record_format | MEDLINE/PubMed |
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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