Serveur d'exploration MERS

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Broad-spectrum antivirals for the emerging Middle East respiratory syndrome coronavirus.

Identifieur interne : 001B65 ( PubMed/Corpus ); précédent : 001B64; suivant : 001B66

Broad-spectrum antivirals for the emerging Middle East respiratory syndrome coronavirus.

Auteurs : Jasper F W. Chan ; Kwok-Hung Chan ; Richard Y T. Kao ; Kelvin K W. To ; Bo-Jian Zheng ; Clara P Y. Li ; Patrick T W. Li ; Jun Dai ; Florence K Y. Mok ; Honglin Chen ; Frederick G. Hayden ; Kwok-Yung Yuen

Source :

RBID : pubmed:24096239

English descriptors

Abstract

Middle East respiratory syndrome coronavirus (MERS-CoV) has emerged to cause fatal infections in patients in the Middle East and traveler-associated secondary cases in Europe and Africa. Person-to-person transmission is evident in outbreaks involving household and hospital contacts. Effective antivirals are urgently needed.

DOI: 10.1016/j.jinf.2013.09.029
PubMed: 24096239

Links to Exploration step

pubmed:24096239

Le document en format XML

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<term>Communicable Diseases, Emerging (drug therapy)</term>
<term>Communicable Diseases, Emerging (virology)</term>
<term>Coronavirus (drug effects)</term>
<term>Coronavirus Infections (drug therapy)</term>
<term>Coronavirus Infections (virology)</term>
<term>Disease Outbreaks</term>
<term>Drug Discovery (methods)</term>
<term>High-Throughput Screening Assays (methods)</term>
<term>Humans</term>
<term>Interferons (pharmacology)</term>
<term>Mycophenolic Acid (pharmacology)</term>
<term>Ribavirin (pharmacology)</term>
<term>Vero Cells</term>
<term>Viral Load (drug effects)</term>
<term>Viral Plaque Assay</term>
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<term>Antiviral Agents</term>
<term>Interferons</term>
<term>Mycophenolic Acid</term>
<term>Ribavirin</term>
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<term>Coronavirus</term>
<term>Viral Load</term>
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<term>Coronavirus Infections</term>
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<term>Coronavirus Infections</term>
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<term>Chlorocebus aethiops</term>
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<front>
<div type="abstract" xml:lang="en">Middle East respiratory syndrome coronavirus (MERS-CoV) has emerged to cause fatal infections in patients in the Middle East and traveler-associated secondary cases in Europe and Africa. Person-to-person transmission is evident in outbreaks involving household and hospital contacts. Effective antivirals are urgently needed.</div>
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<DateCompleted>
<Year>2014</Year>
<Month>07</Month>
<Day>17</Day>
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<DateRevised>
<Year>2020</Year>
<Month>04</Month>
<Day>07</Day>
</DateRevised>
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<ISSN IssnType="Electronic">1532-2742</ISSN>
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<Volume>67</Volume>
<Issue>6</Issue>
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<Year>2013</Year>
<Month>Dec</Month>
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<Title>The Journal of infection</Title>
<ISOAbbreviation>J. Infect.</ISOAbbreviation>
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<ArticleTitle>Broad-spectrum antivirals for the emerging Middle East respiratory syndrome coronavirus.</ArticleTitle>
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<MedlinePgn>606-16</MedlinePgn>
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<AbstractText Label="OBJECTIVES" NlmCategory="OBJECTIVE">Middle East respiratory syndrome coronavirus (MERS-CoV) has emerged to cause fatal infections in patients in the Middle East and traveler-associated secondary cases in Europe and Africa. Person-to-person transmission is evident in outbreaks involving household and hospital contacts. Effective antivirals are urgently needed.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">We used small compound-based forward chemical genetics to screen a chemical library of 1280 known drugs against influenza A virus in Biosafety Level-2 laboratory. We then assessed the anti-MERS-CoV activities of the identified compounds and of interferons, nelfinavir, and lopinavir because of their reported anti-coronavirus activities in terms of cytopathic effect inhibition, viral yield reduction, and plaque reduction assays in Biosafety Level-3 laboratory.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Ten compounds were identified as primary hits in high-throughput screening. Only mycophenolic acid exhibited low EC50 and high selectivity index. Additionally, ribavirin and interferons also exhibited in-vitro anti-MERS-CoV activity. The serum concentrations achievable at therapeutic doses of mycophenolic acid and interferon-β1b were 60-300 and 3-4 times higher than the concentrations at which in-vitro anti-MERS-CoV activities were demonstrated, whereas that of ribavirin was ∼2 times lower. Combination of mycophenolic acid and interferon-β1b lowered the EC50 of each drug by 1-3 times.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Interferon-β1b with mycophenolic acid should be considered in treatment trials of MERS.</AbstractText>
<CopyrightInformation>Copyright © 2013 The British Infection Association. Published by Elsevier Ltd. All rights reserved.</CopyrightInformation>
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<LastName>Chan</LastName>
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<Affiliation>State Key Laboratory of Emerging Infectious Diseases, The University of Hong Kong, Hong Kong, China; Department of Microbiology, The University of Hong Kong, Hong Kong, China; Research Centre of Infection and Immunology, The University of Hong Kong, Hong Kong, China.</Affiliation>
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<QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName>
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<DescriptorName UI="D014709" MajorTopicYN="N">Vero Cells</DescriptorName>
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<DescriptorName UI="D019562" MajorTopicYN="N">Viral Load</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName>
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<DescriptorName UI="D010948" MajorTopicYN="N">Viral Plaque Assay</DescriptorName>
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<Keyword MajorTopicYN="N">Coronavirus</Keyword>
<Keyword MajorTopicYN="N">Interferon</Keyword>
<Keyword MajorTopicYN="N">Middle East</Keyword>
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