Le SIDA au Ghana (serveur d'exploration)

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HIV-1 proteases from drug-naive West African patients are differentially less susceptible to protease inhibitors.

Identifieur interne : 000174 ( Ncbi/Checkpoint ); précédent : 000173; suivant : 000175

HIV-1 proteases from drug-naive West African patients are differentially less susceptible to protease inhibitors.

Auteurs : Masanobu Kinomoto [Japon] ; Regina Appiah-Opong ; J A M. Brandful ; Masaru Yokoyama ; Nicholas Nii-Trebi ; Evelyn Ugly-Kwame ; Hironori Sato ; David Ofori-Adjei ; Takeshi Kurata ; Françoise Barre-Sinoussi ; Tetsutaro Sata ; Kenzo Tokunaga

Source :

RBID : pubmed:15983923

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English descriptors

Abstract

Now that highly active antiretroviral therapy (HAART) is being initiated on a large scale in West Africa, it remains controversial whether protease inhibitors (PIs), originally designed and tested against human immunodeficiency virus type 1 (HIV-1) subtype B, are equally effective against the non-B subtypes that are prevalent in West African countries. In this study, we investigated whether Ghanaian HIV-1 isolates, as representatives of West African isolates, are susceptible to PIs.

DOI: 10.1086/431197
PubMed: 15983923


Affiliations:


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pubmed:15983923

Le document en format XML

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<name sortKey="Kinomoto, Masanobu" sort="Kinomoto, Masanobu" uniqKey="Kinomoto M" first="Masanobu" last="Kinomoto">Masanobu Kinomoto</name>
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<nlm:affiliation>Department of Pathology, National Institute of Infectious Diseases, Tokyo, Japan.</nlm:affiliation>
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<name sortKey="Sato, Hironori" sort="Sato, Hironori" uniqKey="Sato H" first="Hironori" last="Sato">Hironori Sato</name>
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<name sortKey="Barre Sinoussi, Francoise" sort="Barre Sinoussi, Francoise" uniqKey="Barre Sinoussi F" first="Françoise" last="Barre-Sinoussi">Françoise Barre-Sinoussi</name>
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<term>HIV Infections (virology)</term>
<term>HIV Protease (chemistry)</term>
<term>HIV Protease (metabolism)</term>
<term>HIV Protease Inhibitors (pharmacology)</term>
<term>HIV-1 (enzymology)</term>
<term>HIV-1 (genetics)</term>
<term>Humans</term>
<term>Molecular Sequence Data</term>
<term>Phylogeny</term>
<term>Protein Conformation</term>
<term>Sequence Alignment</term>
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<term>Alignement de séquences</term>
<term>Conformation des protéines</term>
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<term>Ghana (épidémiologie)</term>
<term>Humains</term>
<term>Infections à VIH (virologie)</term>
<term>Inhibiteurs de protéase du VIH (pharmacologie)</term>
<term>Multirésistance virale aux médicaments</term>
<term>Phylogénie</term>
<term>Protéase du VIH ()</term>
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<term>Séquence d'acides aminés</term>
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<term>HIV Protease</term>
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<term>Protein Conformation</term>
<term>Sequence Alignment</term>
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<div type="abstract" xml:lang="en">Now that highly active antiretroviral therapy (HAART) is being initiated on a large scale in West Africa, it remains controversial whether protease inhibitors (PIs), originally designed and tested against human immunodeficiency virus type 1 (HIV-1) subtype B, are equally effective against the non-B subtypes that are prevalent in West African countries. In this study, we investigated whether Ghanaian HIV-1 isolates, as representatives of West African isolates, are susceptible to PIs.</div>
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