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- Publisher Website: 10.1016/j.jcv.2004.03.003
- Scopus: eid_2-s2.0-3543143713
- PMID: 15288617
- WOS: WOS:000223456200013
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Article: 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 |
---|---|
Authors | |
Keywords | Antiviral compounds Epidemics Severe acute respiratory syndrome |
Issue Date | 2004 |
Publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/jcv |
Citation | Journal of Clinical Virology, 2004, v. 31 n. 1, p. 69-75 How to Cite? |
Abstract | 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. © 2004 Elsevier B.V. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/163121 |
ISSN | 2023 Impact Factor: 4.0 2023 SCImago Journal Rankings: 1.344 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chen, SF | en_HK |
dc.contributor.author | Chan, KH | en_HK |
dc.contributor.author | Jiang, Y | en_HK |
dc.contributor.author | Kao, RYT | en_HK |
dc.contributor.author | Lu, HT | en_HK |
dc.contributor.author | Fan, KW | en_HK |
dc.contributor.author | Cheng, VCC | en_HK |
dc.contributor.author | Tsui, WHW | en_HK |
dc.contributor.author | Hung, IFN | en_HK |
dc.contributor.author | Lee, TSW | en_HK |
dc.contributor.author | Guan, Y | en_HK |
dc.contributor.author | Peiris, JSM | en_HK |
dc.contributor.author | Yuen, KY | en_HK |
dc.date.accessioned | 2012-09-05T05:27:53Z | - |
dc.date.available | 2012-09-05T05:27:53Z | - |
dc.date.issued | 2004 | en_HK |
dc.identifier.citation | Journal of Clinical Virology, 2004, v. 31 n. 1, p. 69-75 | en_HK |
dc.identifier.issn | 1386-6532 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/163121 | - |
dc.description.abstract | 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. © 2004 Elsevier B.V. All rights reserved. | en_HK |
dc.language | eng | en_US |
dc.publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/jcv | en_HK |
dc.relation.ispartof | Journal of Clinical Virology | en_HK |
dc.rights | Journal of Clinical Virology. Copyright © Elsevier BV. | - |
dc.subject | Antiviral compounds | en_HK |
dc.subject | Epidemics | en_HK |
dc.subject | Severe acute respiratory syndrome | en_HK |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Antiviral Agents - Pharmacology | en_US |
dc.subject.mesh | Cell Line | en_US |
dc.subject.mesh | Chlorogenic Acid - Chemistry - Pharmacology | en_US |
dc.subject.mesh | Drug Synergism | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Flavonoids - Chemistry - Pharmacology | en_US |
dc.subject.mesh | Glycyrrhizic Acid - Chemistry - Pharmacology | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Interferon-Alpha - Pharmacology | en_US |
dc.subject.mesh | Interferon-Beta - Pharmacology | en_US |
dc.subject.mesh | Lopinavir | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Microbial Sensitivity Tests | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Pyrimidinones - Pharmacology | en_US |
dc.subject.mesh | Ribavirin - Pharmacology | en_US |
dc.subject.mesh | Rimantadine - Pharmacology | en_US |
dc.subject.mesh | Sars Virus - Drug Effects | en_US |
dc.subject.mesh | Severe Acute Respiratory Syndrome - Virology | en_US |
dc.subject.mesh | Viral Plaque Assay | en_US |
dc.title | In vitro susceptibility of 10 clinical isolates of SARS coronavirus to selected antiviral compounds | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Chen, SF: sfchen@hku.hk | en_HK |
dc.identifier.email | Kao, RYT: rytkao@hkucc.hku.hk | en_HK |
dc.identifier.email | Fan, KW: keithfan@hkucc.hku.hk | en_HK |
dc.identifier.email | Cheng, VCC: vcccheng@HKUCC.hku.hk | en_HK |
dc.identifier.email | Tsui, WHW: wayne@hkucc.hku.hk | en_HK |
dc.identifier.email | Hung, IFN: ivanhung@hkucc.hku.hk | en_HK |
dc.identifier.email | Guan, Y: yguan@hkucc.hku.hk | - |
dc.identifier.email | Peiris, JSM: malik@hkucc.hku.hk | - |
dc.identifier.email | Yuen, KY: kyyuen@hkucc.hku.hk | - |
dc.identifier.authority | Chen, F=rp00672 | en_HK |
dc.identifier.authority | Kao, RYT=rp00481 | en_HK |
dc.identifier.authority | Hung, IFN=rp00508 | en_HK |
dc.identifier.authority | Guan, Y=rp00397 | en_HK |
dc.identifier.authority | Peiris, JSM=rp00410 | en_HK |
dc.identifier.authority | Yuen, KY=rp00366 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1016/j.jcv.2004.03.003 | en_HK |
dc.identifier.pmid | 15288617 | - |
dc.identifier.scopus | eid_2-s2.0-3543143713 | en_HK |
dc.identifier.hkuros | 106299 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-3543143713&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 31 | en_HK |
dc.identifier.issue | 1 | en_HK |
dc.identifier.spage | 69 | en_HK |
dc.identifier.epage | 75 | en_HK |
dc.identifier.isi | WOS:000223456200013 | - |
dc.publisher.place | Netherlands | en_HK |
dc.identifier.scopusauthorid | Chen, F=7404907980 | en_HK |
dc.identifier.scopusauthorid | Chan, KH=7406034307 | en_HK |
dc.identifier.scopusauthorid | Jiang, Y=24605346600 | en_HK |
dc.identifier.scopusauthorid | Kao, RYT=7101675499 | en_HK |
dc.identifier.scopusauthorid | Lu, HT=55186375200 | en_HK |
dc.identifier.scopusauthorid | Fan, KW=7202978325 | en_HK |
dc.identifier.scopusauthorid | Cheng, VCC=23670479400 | en_HK |
dc.identifier.scopusauthorid | Tsui, WHW=36124344600 | en_HK |
dc.identifier.scopusauthorid | Hung, IFN=7006103457 | en_HK |
dc.identifier.scopusauthorid | Lee, TSW=7501439333 | en_HK |
dc.identifier.scopusauthorid | Guan, Y=7202924055 | en_HK |
dc.identifier.scopusauthorid | Peiris, JSM=7005486823 | en_HK |
dc.identifier.scopusauthorid | Yuen, KY=36078079100 | en_HK |
dc.customcontrol.immutable | sml 130524 | - |
dc.identifier.issnl | 1386-6532 | - |