Expanding the frontiers of existing antiviral drugs: Possible effects of HIV-1 protease inhibitors against SARS and avian influenza
Identifieur interne : 004B32 ( Main/Merge ); précédent : 004B31; suivant : 004B33Expanding the frontiers of existing antiviral drugs: Possible effects of HIV-1 protease inhibitors against SARS and avian influenza
Auteurs : Andrea SavarinoSource :
- Journal of Clinical Virology [ 1386-6532 ] ; 2005.
Descripteurs français
- KwdFr :
- Alignement de séquences, Animaux, Antiviraux (usage thérapeutique), Données de séquences moléculaires, Grippe chez les oiseaux (traitement médicamenteux), Humains, Inhibiteurs de protéase du VIH (usage thérapeutique), Modèles moléculaires, Oiseaux, Structure moléculaire, Syndrome respiratoire aigu sévère (traitement médicamenteux), Séquence d'acides aminés, Virus de la grippe A, Virus du SRAS ().
- MESH :
- traitement médicamenteux : Grippe chez les oiseaux, Syndrome respiratoire aigu sévère.
- usage thérapeutique : Antiviraux, Inhibiteurs de protéase du VIH.
- Alignement de séquences, Animaux, Données de séquences moléculaires, Humains, Modèles moléculaires, Oiseaux, Structure moléculaire, Séquence d'acides aminés, Virus de la grippe A, Virus du SRAS.
English descriptors
- KwdEn :
- Amino Acid Sequence, Animals, Antiviral Agents (therapeutic use), Birds, HIV Protease Inhibitors (therapeutic use), Humans, Influenza A virus, Influenza in Birds (drug therapy), Models, Molecular, Molecular Sequence Data, Molecular Structure, SARS Virus (drug effects), Sequence Alignment, Severe Acute Respiratory Syndrome (drug therapy).
- MESH :
- chemical , therapeutic use : Antiviral Agents, HIV Protease Inhibitors.
- drug effects : SARS Virus.
- drug therapy : Influenza in Birds, Severe Acute Respiratory Syndrome.
- Amino Acid Sequence, Animals, Birds, Humans, Influenza A virus, Models, Molecular, Molecular Sequence Data, Molecular Structure, Sequence Alignment.
Abstract
When unexpected diseases such as the severe acute respiratory syndrome (SARS) and avian influenza become a serious threat to public health, an immediate response is imperative. This should take into consideration existing licensed antiviral drugs against other viral diseases already known to be safe for use in humans. In this report, evidence is presented that HIV-1 protease inhibitors (PIs) currently used in anti-HIV-1 therapies might exert some effects on SARS and perhaps, on avian influenza. Evidence for the potential benefits of PIs against the SARS coronavirus (SARS-CoV) is provided by empirical clinical studies, in vivo viral inhibition assays and computational simulations of the docking of these compounds to the active site of the main SARS-CoV protease. As suggested by in silico docking of these molecules to a theoretical model of a subunit of type A influenza virus RNA-dependent RNA polymerase, there also exists a remote possibility that these PIs may have an effect on avian influenza viruses. Although this evidence is still far from being definitive, the results so far obtained suggest that PIs should be seriously taken into consideration for further testing as potential therapeutic agents for SARS and avian influenza.
Url:
DOI: 10.1016/j.jcv.2005.03.005
PubMed: 15893956
PubMed Central: 7108403
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Links to Exploration step
PMC:7108403Le document en format XML
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xml:lang="en" level="a" type="main">Expanding the frontiers of existing antiviral drugs: Possible effects of HIV-1 protease inhibitors against SARS and avian influenza</title><author><name sortKey="Savarino, Andrea" sort="Savarino, Andrea" uniqKey="Savarino A" first="Andrea" last="Savarino">Andrea Savarino</name></author></analytic><series><title level="j">Journal of Clinical Virology</title><idno type="ISSN">1386-6532</idno><idno type="eISSN">1873-5967</idno><imprint><date when="2005">2005</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Amino Acid Sequence</term><term>Animals</term><term>Antiviral Agents (therapeutic use)</term><term>Birds</term><term>HIV Protease Inhibitors (therapeutic use)</term><term>Humans</term><term>Influenza A virus</term><term>Influenza in Birds (drug therapy)</term><term>Models, Molecular</term><term>Molecular Sequence Data</term><term>Molecular Structure</term><term>SARS Virus (drug effects)</term><term>Sequence Alignment</term><term>Severe Acute Respiratory Syndrome (drug therapy)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Alignement de séquences</term><term>Animaux</term><term>Antiviraux (usage thérapeutique)</term><term>Données de séquences moléculaires</term><term>Grippe chez les oiseaux (traitement médicamenteux)</term><term>Humains</term><term>Inhibiteurs de protéase du VIH (usage thérapeutique)</term><term>Modèles moléculaires</term><term>Oiseaux</term><term>Structure moléculaire</term><term>Syndrome respiratoire aigu sévère (traitement médicamenteux)</term><term>Séquence d'acides aminés</term><term>Virus de la grippe A</term><term>Virus du SRAS ()</term></keywords><keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Antiviral Agents</term><term>HIV Protease Inhibitors</term></keywords><keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>SARS Virus</term></keywords><keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Influenza in Birds</term><term>Severe Acute Respiratory Syndrome</term></keywords><keywords scheme="MESH" qualifier="traitement médicamenteux" xml:lang="fr"><term>Grippe chez les oiseaux</term><term>Syndrome respiratoire aigu sévère</term></keywords><keywords scheme="MESH" qualifier="usage thérapeutique" xml:lang="fr"><term>Antiviraux</term><term>Inhibiteurs de protéase du VIH</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Amino Acid Sequence</term><term>Animals</term><term>Birds</term><term>Humans</term><term>Influenza A virus</term><term>Models, Molecular</term><term>Molecular Sequence Data</term><term>Molecular Structure</term><term>Sequence Alignment</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Alignement de séquences</term><term>Animaux</term><term>Données de séquences moléculaires</term><term>Humains</term><term>Modèles moléculaires</term><term>Oiseaux</term><term>Structure moléculaire</term><term>Séquence d'acides aminés</term><term>Virus de la grippe A</term><term>Virus du SRAS</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>When unexpected diseases such as the severe acute respiratory syndrome (SARS) and avian influenza become a serious threat to public health, an immediate response is imperative. This should take into consideration existing licensed antiviral drugs against other viral diseases already known to be safe for use in humans. In this report, evidence is presented that HIV-1 protease inhibitors (PIs) currently used in anti-HIV-1 therapies might exert some effects on SARS and perhaps, on avian influenza. Evidence for the potential benefits of PIs against the SARS coronavirus (SARS-CoV) is provided by empirical clinical studies, in vivo viral inhibition assays and computational simulations of the docking of these compounds to the active site of the main SARS-CoV protease. As suggested by in silico docking of these molecules to a theoretical model of a subunit of type A influenza virus RNA-dependent RNA polymerase, there also exists a remote possibility that these PIs may have an effect on avian influenza viruses. Although this evidence is still far from being definitive, the results so far obtained suggest that PIs should be seriously taken into consideration for further testing as potential therapeutic agents for SARS and avian influenza.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Anand, K" uniqKey="Anand K">K. Anand</name></author><author><name sortKey="Ziebuhr, J" uniqKey="Ziebuhr J">J. Ziebuhr</name></author><author><name sortKey="Wadhwani, P" uniqKey="Wadhwani P">P. Wadhwani</name></author><author><name sortKey="Mesters, J R" uniqKey="Mesters J">J.R. Mesters</name></author><author><name sortKey="Hilgenfeld, R" uniqKey="Hilgenfeld R">R. Hilgenfeld</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Cassone, A" uniqKey="Cassone A">A. Cassone</name></author><author><name sortKey="De Bernardis, F" uniqKey="De Bernardis F">F. 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Zhou</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Zhang, X W" uniqKey="Zhang X">X.W. Zhang</name></author><author><name sortKey="Yap, Y L" uniqKey="Yap Y">Y.L. Yap</name></author></analytic></biblStruct></listBibl></div1></back></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Merge/RBID.i -Sk "pubmed:15893956" \
| HfdSelect -Kh $EXPLOR_AREA/Data/Main/Merge/biblio.hfd \
| NlmPubMed2Wicri -a SrasV1
| This area was generated with Dilib version V0.6.33. |  |