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SARS coronavirus anti-infectives.

Identifieur interne : 001B61 ( Ncbi/Curation ); précédent : 001B60; suivant : 001B62

SARS coronavirus anti-infectives.

Auteurs : Tommy R. Tong [Hong Kong]

Source :

RBID : pubmed:18221155

Descripteurs français

English descriptors

Abstract

Severe acute respiratory syndrome (SARS) emerged in late 2002 and was controlled in July 2003 by public health measures. Its causative agent, SARS coronavirus (SARS-CoV) jumped from an animal reservoir to humans and has the potential to re-emerge. Following the sequencing of the genetic code and the deciphering of some of the functions of its proteins, including the cellular receptors and host proteins that participate in the life cycle of the virus, promising lead drugs and new uses of old drugs have been discovered. Patent applications for cathepsin L inhibitors have taken new relevance because of the role of cathepsin L in the entry of SARS-CoV into host cells. Likewise, patent applications for SARS-CoV protease inhibitors and interferon and mismatched dsRNA also need to be watched for potential application in treatment and prevention of SARS-CoV. Here, we review the recent advances and inventions that target SARS-CoV infection in humans.

DOI: 10.2174/157489106778777637
PubMed: 18221155

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pubmed:18221155

Le document en format XML

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<nlm:affiliation>Department of Pathology, Princess Margaret Hospital, Hong Kong. tommy.tong@yahoo.com</nlm:affiliation>
<country xml:lang="fr">Hong Kong</country>
<wicri:regionArea>Department of Pathology, Princess Margaret Hospital</wicri:regionArea>
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<term>DNA Helicases (antagonists & inhibitors)</term>
<term>DNA-Directed RNA Polymerases (antagonists & inhibitors)</term>
<term>Humans</term>
<term>Interferons (pharmacology)</term>
<term>Protease Inhibitors (pharmacology)</term>
<term>SARS Virus (drug effects)</term>
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<term>Severe Acute Respiratory Syndrome (virology)</term>
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<term>Animaux</term>
<term>Anticorps monoclonaux (pharmacologie)</term>
<term>Antiviraux (usage thérapeutique)</term>
<term>DNA-directed RNA polymerases (antagonistes et inhibiteurs)</term>
<term>Helicase (antagonistes et inhibiteurs)</term>
<term>Humains</term>
<term>Inhibiteurs de protéases (pharmacologie)</term>
<term>Interférons (pharmacologie)</term>
<term>Syndrome respiratoire aigu sévère (traitement médicamenteux)</term>
<term>Syndrome respiratoire aigu sévère (virologie)</term>
<term>Virus du SRAS ()</term>
<term>Virus du SRAS (pathogénicité)</term>
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<term>DNA Helicases</term>
<term>DNA-Directed RNA Polymerases</term>
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<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en">
<term>Antibodies, Monoclonal</term>
<term>Interferons</term>
<term>Protease Inhibitors</term>
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<keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en">
<term>Antiviral Agents</term>
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<keywords scheme="MESH" qualifier="antagonistes et inhibiteurs" xml:lang="fr">
<term>DNA-directed RNA polymerases</term>
<term>Helicase</term>
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<keywords scheme="MESH" qualifier="drug effects" xml:lang="en">
<term>SARS Virus</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en">
<term>Severe Acute Respiratory Syndrome</term>
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<keywords scheme="MESH" qualifier="pathogenicity" xml:lang="en">
<term>SARS Virus</term>
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<keywords scheme="MESH" qualifier="pathogénicité" xml:lang="fr">
<term>Virus du SRAS</term>
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<term>Anticorps monoclonaux</term>
<term>Inhibiteurs de protéases</term>
<term>Interférons</term>
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<term>Syndrome respiratoire aigu sévère</term>
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<term>Antiviraux</term>
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<term>Syndrome respiratoire aigu sévère</term>
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<term>Severe Acute Respiratory Syndrome</term>
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<div type="abstract" xml:lang="en">Severe acute respiratory syndrome (SARS) emerged in late 2002 and was controlled in July 2003 by public health measures. Its causative agent, SARS coronavirus (SARS-CoV) jumped from an animal reservoir to humans and has the potential to re-emerge. Following the sequencing of the genetic code and the deciphering of some of the functions of its proteins, including the cellular receptors and host proteins that participate in the life cycle of the virus, promising lead drugs and new uses of old drugs have been discovered. Patent applications for cathepsin L inhibitors have taken new relevance because of the role of cathepsin L in the entry of SARS-CoV into host cells. Likewise, patent applications for SARS-CoV protease inhibitors and interferon and mismatched dsRNA also need to be watched for potential application in treatment and prevention of SARS-CoV. Here, we review the recent advances and inventions that target SARS-CoV infection in humans.</div>
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