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HIV-1 Entry, Inhibitors, and Resistance

Entry inhibitors represent a new class of antiretroviral agents for the treatment of infection with HIV-1. While resistance to other HIV drug classes has been well described, resistance to this new class is still ill defined despite considerable clinical use. Several potential mechanisms have been p...

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Detalles Bibliográficos
Autores principales: Lobritz, Michael A., Ratcliff, Annette N., Arts, Eric J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3187606/
https://www.ncbi.nlm.nih.gov/pubmed/21994672
http://dx.doi.org/10.3390/v2051069
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author Lobritz, Michael A.
Ratcliff, Annette N.
Arts, Eric J.
author_facet Lobritz, Michael A.
Ratcliff, Annette N.
Arts, Eric J.
author_sort Lobritz, Michael A.
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description Entry inhibitors represent a new class of antiretroviral agents for the treatment of infection with HIV-1. While resistance to other HIV drug classes has been well described, resistance to this new class is still ill defined despite considerable clinical use. Several potential mechanisms have been proposed: tropism switching (utilization of CXCR4 instead of CCR5 for entry), increased affinity for the coreceptor, increased rate of virus entry into host cells, and utilization of inhibitor-bound receptor for entry. In this review we will address the development of attachment, fusion, and coreceptor entry inhibitors and explore recent studies describing potential mechanisms of resistance.
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spelling pubmed-31876062011-10-12 HIV-1 Entry, Inhibitors, and Resistance Lobritz, Michael A. Ratcliff, Annette N. Arts, Eric J. Viruses Review Entry inhibitors represent a new class of antiretroviral agents for the treatment of infection with HIV-1. While resistance to other HIV drug classes has been well described, resistance to this new class is still ill defined despite considerable clinical use. Several potential mechanisms have been proposed: tropism switching (utilization of CXCR4 instead of CCR5 for entry), increased affinity for the coreceptor, increased rate of virus entry into host cells, and utilization of inhibitor-bound receptor for entry. In this review we will address the development of attachment, fusion, and coreceptor entry inhibitors and explore recent studies describing potential mechanisms of resistance. Molecular Diversity Preservation International (MDPI) 2010-04-29 /pmc/articles/PMC3187606/ /pubmed/21994672 http://dx.doi.org/10.3390/v2051069 Text en © 2010 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
Lobritz, Michael A.
Ratcliff, Annette N.
Arts, Eric J.
HIV-1 Entry, Inhibitors, and Resistance
title HIV-1 Entry, Inhibitors, and Resistance
title_full HIV-1 Entry, Inhibitors, and Resistance
title_fullStr HIV-1 Entry, Inhibitors, and Resistance
title_full_unstemmed HIV-1 Entry, Inhibitors, and Resistance
title_short HIV-1 Entry, Inhibitors, and Resistance
title_sort hiv-1 entry, inhibitors, and resistance
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3187606/
https://www.ncbi.nlm.nih.gov/pubmed/21994672
http://dx.doi.org/10.3390/v2051069
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