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HIV-1 Diversity in the Envelope Glycoproteins: Implications for Viral Entry Inhibition

Entry of HIV-1 into a host cell is a multi-step process, with the viral envelope gp120 and gp41 acting sequentially to mediate the viral attachment, CD4 binding, coreceptor binding, and fusion of the viral and host membranes. The emerging class of antiretroviral agents, collectively known as entry i...

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Detalles Bibliográficos
Autores principales: Araújo, Leonardo Augusto Luvison, Almeida, Sabrina E. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3640516/
https://www.ncbi.nlm.nih.gov/pubmed/23389465
http://dx.doi.org/10.3390/v5020595
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author Araújo, Leonardo Augusto Luvison
Almeida, Sabrina E. M.
author_facet Araújo, Leonardo Augusto Luvison
Almeida, Sabrina E. M.
author_sort Araújo, Leonardo Augusto Luvison
collection PubMed
description Entry of HIV-1 into a host cell is a multi-step process, with the viral envelope gp120 and gp41 acting sequentially to mediate the viral attachment, CD4 binding, coreceptor binding, and fusion of the viral and host membranes. The emerging class of antiretroviral agents, collectively known as entry inhibitors, interfere in some of these steps. However, viral diversity has implications for possible differential responses to entry inhibitors, since envelope is the most variable of all HIV genes. Different HIV genetic forms carry in their genomes genetic signatures and polymorphisms that could alter the structure of viral proteins which are targeted by drugs, thus impairing antiretroviral binding and efficacy. This review will examine current research that describes subtype differences in envelope at the genetic level and the effects of mutations on the efficacy of current entry inhibitors.
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spelling pubmed-36405162013-05-03 HIV-1 Diversity in the Envelope Glycoproteins: Implications for Viral Entry Inhibition Araújo, Leonardo Augusto Luvison Almeida, Sabrina E. M. Viruses Review Entry of HIV-1 into a host cell is a multi-step process, with the viral envelope gp120 and gp41 acting sequentially to mediate the viral attachment, CD4 binding, coreceptor binding, and fusion of the viral and host membranes. The emerging class of antiretroviral agents, collectively known as entry inhibitors, interfere in some of these steps. However, viral diversity has implications for possible differential responses to entry inhibitors, since envelope is the most variable of all HIV genes. Different HIV genetic forms carry in their genomes genetic signatures and polymorphisms that could alter the structure of viral proteins which are targeted by drugs, thus impairing antiretroviral binding and efficacy. This review will examine current research that describes subtype differences in envelope at the genetic level and the effects of mutations on the efficacy of current entry inhibitors. MDPI 2013-02-06 /pmc/articles/PMC3640516/ /pubmed/23389465 http://dx.doi.org/10.3390/v5020595 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Araújo, Leonardo Augusto Luvison
Almeida, Sabrina E. M.
HIV-1 Diversity in the Envelope Glycoproteins: Implications for Viral Entry Inhibition
title HIV-1 Diversity in the Envelope Glycoproteins: Implications for Viral Entry Inhibition
title_full HIV-1 Diversity in the Envelope Glycoproteins: Implications for Viral Entry Inhibition
title_fullStr HIV-1 Diversity in the Envelope Glycoproteins: Implications for Viral Entry Inhibition
title_full_unstemmed HIV-1 Diversity in the Envelope Glycoproteins: Implications for Viral Entry Inhibition
title_short HIV-1 Diversity in the Envelope Glycoproteins: Implications for Viral Entry Inhibition
title_sort hiv-1 diversity in the envelope glycoproteins: implications for viral entry inhibition
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3640516/
https://www.ncbi.nlm.nih.gov/pubmed/23389465
http://dx.doi.org/10.3390/v5020595
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