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Indomethacin has a potent antiviral activity against SARS coronavirus.

Identifieur interne : 001E95 ( PubMed/Curation ); précédent : 001E94; suivant : 001E96

Indomethacin has a potent antiviral activity against SARS coronavirus.

Auteurs : Carla Amici [Italie] ; Antonino Di Caro ; Alessandra Ciucci ; Lucia Chiappa ; Concetta Castilletti ; Vito Martella ; Nicola Decaro ; Canio Buonavoglia ; Maria R. Capobianchi ; M Gabriella Santoro

Source :

RBID : pubmed:17302372

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English descriptors

Abstract

Severe acute respiratory syndrome (SARS) is a newly emerging, highly transmissible and fatal disease caused by a previously unknown coronavirus (SARS-CoV). Existing in non-identified animal reservoirs, SARS-CoV continues to represent a threat to humans because there is no effective specific antiviral therapy for coronavirus infections.

PubMed: 17302372

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pubmed:17302372

Le document en format XML

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<term>Dogs</term>
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<term>Antiviraux (usage thérapeutique)</term>
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<term>Coronavirus canin ()</term>
<term>Fèces (virologie)</term>
<term>Humains</term>
<term>Indométacine (pharmacologie)</term>
<term>Indométacine (usage thérapeutique)</term>
<term>Infections à coronavirus (médecine vétérinaire)</term>
<term>Infections à coronavirus (traitement médicamenteux)</term>
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<term>Antiviral Agents</term>
<term>Aspirin</term>
<term>Indomethacin</term>
<term>Interferon-alpha</term>
<term>Ribavirin</term>
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<term>Antiviral Agents</term>
<term>Indomethacin</term>
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<term>Coronavirus, Canine</term>
<term>SARS Virus</term>
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<term>Infections à coronavirus</term>
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<term>Acide acétylsalicylique</term>
<term>Antiviraux</term>
<term>Indométacine</term>
<term>Interféron alpha</term>
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<term>Antiviraux</term>
<term>Indométacine</term>
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<term>Coronavirus Infections</term>
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<term>Feces</term>
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<term>Animals</term>
<term>Cell Line</term>
<term>Chlorocebus aethiops</term>
<term>Dogs</term>
<term>Dose-Response Relationship, Drug</term>
<term>Humans</term>
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<term>Animaux</term>
<term>Chiens</term>
<term>Coronavirus canin</term>
<term>Humains</term>
<term>Lignée cellulaire</term>
<term>Relation dose-effet des médicaments</term>
<term>Réplication virale</term>
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<front>
<div type="abstract" xml:lang="en">Severe acute respiratory syndrome (SARS) is a newly emerging, highly transmissible and fatal disease caused by a previously unknown coronavirus (SARS-CoV). Existing in non-identified animal reservoirs, SARS-CoV continues to represent a threat to humans because there is no effective specific antiviral therapy for coronavirus infections.</div>
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<DateCompleted>
<Year>2007</Year>
<Month>03</Month>
<Day>16</Day>
</DateCompleted>
<DateRevised>
<Year>2019</Year>
<Month>12</Month>
<Day>10</Day>
</DateRevised>
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<ISSN IssnType="Print">1359-6535</ISSN>
<JournalIssue CitedMedium="Print">
<Volume>11</Volume>
<Issue>8</Issue>
<PubDate>
<Year>2006</Year>
</PubDate>
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<Title>Antiviral therapy</Title>
<ISOAbbreviation>Antivir. Ther. (Lond.)</ISOAbbreviation>
</Journal>
<ArticleTitle>Indomethacin has a potent antiviral activity against SARS coronavirus.</ArticleTitle>
<Pagination>
<MedlinePgn>1021-30</MedlinePgn>
</Pagination>
<Abstract>
<AbstractText Label="UNLABELLED">Severe acute respiratory syndrome (SARS) is a newly emerging, highly transmissible and fatal disease caused by a previously unknown coronavirus (SARS-CoV). Existing in non-identified animal reservoirs, SARS-CoV continues to represent a threat to humans because there is no effective specific antiviral therapy for coronavirus infections.</AbstractText>
<AbstractText Label="OBJECTIVES" NlmCategory="OBJECTIVE">Starting from the observation that cyclopentenone cyclooxygenase (COX) metabolites are active against several RNA viruses, we investigated the effect of the COX inhibitor indomethacin on coronavirus replication.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Work involving infectious SARS-CoV was performed in biosafety level 3 facilities. SARS-CoV was grown in monkey VERO cells and human lung epithelial A549 cells, while canine coronavirus (CCoV) was grown in A72 canine cells. Antiviral activity was analysed by determining infective virus titres by TCID50, viral RNA synthesis by Northern blot analysis and real-time RT-PCR, and viral protein synthesis by SDS-PAGE analysis after 35S-methionine-labelling. Antiviral efficacy in vivo was determined by evaluating virus titres in CCoV-infected dogs treated orally with 1 mg/kg body weight indomethacin (INDO).</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Unexpectedly, we found that INDO has a potent direct antiviral activity against the coronaviruses SARS-CoV and CCoV. INDO does not affect coronavirus binding or entry into host cells, but acts by blocking viral RNA synthesis at cytoprotective doses. This effect is independent of cyclooxygenase inhibition. INDO's potent antiviral activity (>1,000-fold reduction in virus yield) was confirmed in vivo in CCoV-infected dogs.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">The results identify INDO as a potent inhibitor of coronavirus replication and suggest that, having both anti-inflammatory and antiviral activity, INDO could be beneficial in SARS therapy.</AbstractText>
</Abstract>
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<LastName>Amici</LastName>
<ForeName>Carla</ForeName>
<Initials>C</Initials>
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<Affiliation>Department of Biology, University of Rome Tor Vergata, Rome, Italy.</Affiliation>
</AffiliationInfo>
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<LastName>Di Caro</LastName>
<ForeName>Antonino</ForeName>
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<LastName>Ciucci</LastName>
<ForeName>Alessandra</ForeName>
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</Author>
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<ForeName>Maria R</ForeName>
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</Author>
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<ForeName>M Gabriella</ForeName>
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<Language>eng</Language>
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<DescriptorName UI="D045473" MajorTopicYN="N">SARS Virus</DescriptorName>
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</MeshHeading>
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