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In vitro efficacy of artemisinin-based treatments against SARS-CoV-2
Effective and affordable treatments for patients suffering from coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), are needed. We report in vitro efficacy of Artemisia annua extracts as well as artemisinin, artesunate, and artemether against...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8285423/ https://www.ncbi.nlm.nih.gov/pubmed/34272426 http://dx.doi.org/10.1038/s41598-021-93361-y |
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author | Zhou, Yuyong Gilmore, Kerry Ramirez, Santseharay Settels, Eva Gammeltoft, Karen A. Pham, Long V. Fahnøe, Ulrik Feng, Shan Offersgaard, Anna Trimpert, Jakob Bukh, Jens Osterrieder, Klaus Gottwein, Judith M. Seeberger, Peter H. |
author_facet | Zhou, Yuyong Gilmore, Kerry Ramirez, Santseharay Settels, Eva Gammeltoft, Karen A. Pham, Long V. Fahnøe, Ulrik Feng, Shan Offersgaard, Anna Trimpert, Jakob Bukh, Jens Osterrieder, Klaus Gottwein, Judith M. Seeberger, Peter H. |
author_sort | Zhou, Yuyong |
collection | PubMed |
description | Effective and affordable treatments for patients suffering from coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), are needed. We report in vitro efficacy of Artemisia annua extracts as well as artemisinin, artesunate, and artemether against SARS-CoV-2. The latter two are approved active pharmaceutical ingredients of anti-malarial drugs. Concentration–response antiviral treatment assays, based on immunostaining of SARS-CoV-2 spike glycoprotein, revealed that treatment with all studied extracts and compounds inhibited SARS-CoV-2 infection of VeroE6 cells, human hepatoma Huh7.5 cells and human lung cancer A549-hACE2 cells, without obvious influence of the cell type on antiviral efficacy. In treatment assays, artesunate proved most potent (range of 50% effective concentrations (EC(50)) in different cell types: 7–12 µg/mL), followed by artemether (53–98 µg/mL), A. annua extracts (83–260 µg/mL) and artemisinin (151 to at least 208 µg/mL). The selectivity indices (SI), calculated based on treatment and cell viability assays, were mostly below 10 (range 2 to 54), suggesting a small therapeutic window. Time-of-addition experiments in A549-hACE2 cells revealed that artesunate targeted SARS-CoV-2 at the post-entry level. Peak plasma concentrations of artesunate exceeding EC(50) values can be achieved. Clinical studies are required to further evaluate the utility of these compounds as COVID-19 treatment. |
format | Online Article Text |
id | pubmed-8285423 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82854232021-07-19 In vitro efficacy of artemisinin-based treatments against SARS-CoV-2 Zhou, Yuyong Gilmore, Kerry Ramirez, Santseharay Settels, Eva Gammeltoft, Karen A. Pham, Long V. Fahnøe, Ulrik Feng, Shan Offersgaard, Anna Trimpert, Jakob Bukh, Jens Osterrieder, Klaus Gottwein, Judith M. Seeberger, Peter H. Sci Rep Article Effective and affordable treatments for patients suffering from coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), are needed. We report in vitro efficacy of Artemisia annua extracts as well as artemisinin, artesunate, and artemether against SARS-CoV-2. The latter two are approved active pharmaceutical ingredients of anti-malarial drugs. Concentration–response antiviral treatment assays, based on immunostaining of SARS-CoV-2 spike glycoprotein, revealed that treatment with all studied extracts and compounds inhibited SARS-CoV-2 infection of VeroE6 cells, human hepatoma Huh7.5 cells and human lung cancer A549-hACE2 cells, without obvious influence of the cell type on antiviral efficacy. In treatment assays, artesunate proved most potent (range of 50% effective concentrations (EC(50)) in different cell types: 7–12 µg/mL), followed by artemether (53–98 µg/mL), A. annua extracts (83–260 µg/mL) and artemisinin (151 to at least 208 µg/mL). The selectivity indices (SI), calculated based on treatment and cell viability assays, were mostly below 10 (range 2 to 54), suggesting a small therapeutic window. Time-of-addition experiments in A549-hACE2 cells revealed that artesunate targeted SARS-CoV-2 at the post-entry level. Peak plasma concentrations of artesunate exceeding EC(50) values can be achieved. Clinical studies are required to further evaluate the utility of these compounds as COVID-19 treatment. Nature Publishing Group UK 2021-07-16 /pmc/articles/PMC8285423/ /pubmed/34272426 http://dx.doi.org/10.1038/s41598-021-93361-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zhou, Yuyong Gilmore, Kerry Ramirez, Santseharay Settels, Eva Gammeltoft, Karen A. Pham, Long V. Fahnøe, Ulrik Feng, Shan Offersgaard, Anna Trimpert, Jakob Bukh, Jens Osterrieder, Klaus Gottwein, Judith M. Seeberger, Peter H. In vitro efficacy of artemisinin-based treatments against SARS-CoV-2 |
title | In vitro efficacy of artemisinin-based treatments against SARS-CoV-2 |
title_full | In vitro efficacy of artemisinin-based treatments against SARS-CoV-2 |
title_fullStr | In vitro efficacy of artemisinin-based treatments against SARS-CoV-2 |
title_full_unstemmed | In vitro efficacy of artemisinin-based treatments against SARS-CoV-2 |
title_short | In vitro efficacy of artemisinin-based treatments against SARS-CoV-2 |
title_sort | in vitro efficacy of artemisinin-based treatments against sars-cov-2 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8285423/ https://www.ncbi.nlm.nih.gov/pubmed/34272426 http://dx.doi.org/10.1038/s41598-021-93361-y |
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