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In vitro susceptibility of 10 clinical isolates of SARS coronavirus to selected antiviral compounds
Effective antiviral agents are urgently needed to combat the possible return of severe acute respiratory syndrome (SARS). Commercial antiviral agents and pure chemical compounds extracted from traditional Chinese medicinal herbs were screened against 10 clinical isolates of SARS coronavirus by neutr...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7128415/ https://www.ncbi.nlm.nih.gov/pubmed/15288617 http://dx.doi.org/10.1016/j.jcv.2004.03.003 |
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author | Chen, F Chan, K.H Jiang, Y Kao, R.Y.T Lu, H.T Fan, K.W Cheng, V.C.C Tsui, W.H.W Hung, I.F.N Lee, T.S.W Guan, Y Peiris, J.S.M Yuen, K.Y |
author_facet | Chen, F Chan, K.H Jiang, Y Kao, R.Y.T Lu, H.T Fan, K.W Cheng, V.C.C Tsui, W.H.W Hung, I.F.N Lee, T.S.W Guan, Y Peiris, J.S.M Yuen, K.Y |
author_sort | Chen, F |
collection | PubMed |
description | Effective antiviral agents are urgently needed to combat the possible return of severe acute respiratory syndrome (SARS). Commercial antiviral agents and pure chemical compounds extracted from traditional Chinese medicinal herbs were screened against 10 clinical isolates of SARS coronavirus by neutralisation tests with confirmation by plaque reduction assays. Interferon-beta-1a, leukocytic interferon-alpha, ribavirin, lopinavir, rimantadine, baicalin and glycyrrhizin showed antiviral activity. The two interferons were only active if the cell lines were pre-incubated with the drugs 16 h before viral inoculation. Results were confirmed by plaque reduction assays. Antiviral activity varied with the use of different cell lines. Checkerboard assays for synergy were performed showing combinations of interferon beta-1a or leukocytic interferon-alpha with ribavirin are synergistic. Since the clinical and toxicity profiles of these agents are well known, they should be considered either singly or in combination for prophylaxis or treatment of SARS in randomised placebo controlled trials in future epidemics. |
format | Online Article Text |
id | pubmed-7128415 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71284152020-04-08 In vitro susceptibility of 10 clinical isolates of SARS coronavirus to selected antiviral compounds Chen, F Chan, K.H Jiang, Y Kao, R.Y.T Lu, H.T Fan, K.W Cheng, V.C.C Tsui, W.H.W Hung, I.F.N Lee, T.S.W Guan, Y Peiris, J.S.M Yuen, K.Y J Clin Virol Short Communication Effective antiviral agents are urgently needed to combat the possible return of severe acute respiratory syndrome (SARS). Commercial antiviral agents and pure chemical compounds extracted from traditional Chinese medicinal herbs were screened against 10 clinical isolates of SARS coronavirus by neutralisation tests with confirmation by plaque reduction assays. Interferon-beta-1a, leukocytic interferon-alpha, ribavirin, lopinavir, rimantadine, baicalin and glycyrrhizin showed antiviral activity. The two interferons were only active if the cell lines were pre-incubated with the drugs 16 h before viral inoculation. Results were confirmed by plaque reduction assays. Antiviral activity varied with the use of different cell lines. Checkerboard assays for synergy were performed showing combinations of interferon beta-1a or leukocytic interferon-alpha with ribavirin are synergistic. Since the clinical and toxicity profiles of these agents are well known, they should be considered either singly or in combination for prophylaxis or treatment of SARS in randomised placebo controlled trials in future epidemics. Elsevier B.V. 2004-09 2004-05-18 /pmc/articles/PMC7128415/ /pubmed/15288617 http://dx.doi.org/10.1016/j.jcv.2004.03.003 Text en Copyright © 2004 Elsevier B.V. All rights reserved. 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 | Short Communication Chen, F Chan, K.H Jiang, Y Kao, R.Y.T Lu, H.T Fan, K.W Cheng, V.C.C Tsui, W.H.W Hung, I.F.N Lee, T.S.W Guan, Y Peiris, J.S.M Yuen, K.Y In vitro susceptibility of 10 clinical isolates of SARS coronavirus to selected antiviral compounds |
title | In vitro susceptibility of 10 clinical isolates of SARS coronavirus to selected antiviral compounds |
title_full | In vitro susceptibility of 10 clinical isolates of SARS coronavirus to selected antiviral compounds |
title_fullStr | In vitro susceptibility of 10 clinical isolates of SARS coronavirus to selected antiviral compounds |
title_full_unstemmed | In vitro susceptibility of 10 clinical isolates of SARS coronavirus to selected antiviral compounds |
title_short | In vitro susceptibility of 10 clinical isolates of SARS coronavirus to selected antiviral compounds |
title_sort | in vitro susceptibility of 10 clinical isolates of sars coronavirus to selected antiviral compounds |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7128415/ https://www.ncbi.nlm.nih.gov/pubmed/15288617 http://dx.doi.org/10.1016/j.jcv.2004.03.003 |
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