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Inhibition of novel β coronavirus replication by a combination of interferon-α2b and ribavirin
The identification of a novel β coronavirus, nCoV, as the causative agent of severe respiratory illness in humans originating in Saudi Arabia, Qatar and Jordan has raised concerns about the possibility of a coronavirus pandemic similar to that of SARS-CoV. As a definitive treatment regimen has never...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3629412/ https://www.ncbi.nlm.nih.gov/pubmed/23594967 http://dx.doi.org/10.1038/srep01686 |
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author | Falzarano, Darryl de Wit, Emmie Martellaro, Cynthia Callison, Julie Munster, Vincent J. Feldmann, Heinz |
author_facet | Falzarano, Darryl de Wit, Emmie Martellaro, Cynthia Callison, Julie Munster, Vincent J. Feldmann, Heinz |
author_sort | Falzarano, Darryl |
collection | PubMed |
description | The identification of a novel β coronavirus, nCoV, as the causative agent of severe respiratory illness in humans originating in Saudi Arabia, Qatar and Jordan has raised concerns about the possibility of a coronavirus pandemic similar to that of SARS-CoV. As a definitive treatment regimen has never been thoroughly evaluated for coronavirus infections, there is an urgent need to rapidly identify potential therapeutics to address future cases of nCoV. To determine an intervention strategy, the effect of interferon-α2b and ribavirin on nCoV isolate hCoV-EMC/2012 replication in Vero and LLC-MK2 cells was evaluated. hCoV-EMC/2012 was sensitive to both interferon-α2b and ribavirin alone in Vero and LLC-MK2 cells, but only at relatively high concentrations; however, when combined, lower concentrations of interferon-α2b and ribavirin achieved comparable endpoints. Thus, a combination of interferon-α2b and ribavirin, which are already commonly used in the clinic, may be useful for patient management in the event of future nCoV infections. |
format | Online Article Text |
id | pubmed-3629412 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-36294122013-04-18 Inhibition of novel β coronavirus replication by a combination of interferon-α2b and ribavirin Falzarano, Darryl de Wit, Emmie Martellaro, Cynthia Callison, Julie Munster, Vincent J. Feldmann, Heinz Sci Rep Article The identification of a novel β coronavirus, nCoV, as the causative agent of severe respiratory illness in humans originating in Saudi Arabia, Qatar and Jordan has raised concerns about the possibility of a coronavirus pandemic similar to that of SARS-CoV. As a definitive treatment regimen has never been thoroughly evaluated for coronavirus infections, there is an urgent need to rapidly identify potential therapeutics to address future cases of nCoV. To determine an intervention strategy, the effect of interferon-α2b and ribavirin on nCoV isolate hCoV-EMC/2012 replication in Vero and LLC-MK2 cells was evaluated. hCoV-EMC/2012 was sensitive to both interferon-α2b and ribavirin alone in Vero and LLC-MK2 cells, but only at relatively high concentrations; however, when combined, lower concentrations of interferon-α2b and ribavirin achieved comparable endpoints. Thus, a combination of interferon-α2b and ribavirin, which are already commonly used in the clinic, may be useful for patient management in the event of future nCoV infections. Nature Publishing Group 2013-04-18 /pmc/articles/PMC3629412/ /pubmed/23594967 http://dx.doi.org/10.1038/srep01686 Text en Copyright © 2013, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareALike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Article Falzarano, Darryl de Wit, Emmie Martellaro, Cynthia Callison, Julie Munster, Vincent J. Feldmann, Heinz Inhibition of novel β coronavirus replication by a combination of interferon-α2b and ribavirin |
title | Inhibition of novel β coronavirus replication by a combination of interferon-α2b and ribavirin |
title_full | Inhibition of novel β coronavirus replication by a combination of interferon-α2b and ribavirin |
title_fullStr | Inhibition of novel β coronavirus replication by a combination of interferon-α2b and ribavirin |
title_full_unstemmed | Inhibition of novel β coronavirus replication by a combination of interferon-α2b and ribavirin |
title_short | Inhibition of novel β coronavirus replication by a combination of interferon-α2b and ribavirin |
title_sort | inhibition of novel β coronavirus replication by a combination of interferon-α2b and ribavirin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3629412/ https://www.ncbi.nlm.nih.gov/pubmed/23594967 http://dx.doi.org/10.1038/srep01686 |
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