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Purinergic Receptors: Key Mediators of HIV-1 Infection and Inflammation

Human immunodeficiency virus type 1 (HIV-1) causes a chronic infection that afflicts more than 30 million individuals worldwide. While the infection can be suppressed with potent antiretroviral therapies, individuals infected with HIV-1 have elevated levels of inflammation as indicated by increased...

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Autores principales: Swartz, Talia H., Dubyak, George R., Chen, Benjamin K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4659914/
https://www.ncbi.nlm.nih.gov/pubmed/26635799
http://dx.doi.org/10.3389/fimmu.2015.00585
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author Swartz, Talia H.
Dubyak, George R.
Chen, Benjamin K.
author_facet Swartz, Talia H.
Dubyak, George R.
Chen, Benjamin K.
author_sort Swartz, Talia H.
collection PubMed
description Human immunodeficiency virus type 1 (HIV-1) causes a chronic infection that afflicts more than 30 million individuals worldwide. While the infection can be suppressed with potent antiretroviral therapies, individuals infected with HIV-1 have elevated levels of inflammation as indicated by increased T cell activation, soluble biomarkers, and associated morbidity and mortality. A single mechanism linking HIV-1 pathogenesis to this inflammation has yet to be identified. Purinergic receptors are known to mediate inflammation and have been shown to be required for HIV-1 infection at the level of HIV-1 membrane fusion. Here, we review the literature on the role of purinergic receptors in HIV-1 infection and associated inflammation and describe a role for these receptors as potential therapeutic targets.
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spelling pubmed-46599142015-12-03 Purinergic Receptors: Key Mediators of HIV-1 Infection and Inflammation Swartz, Talia H. Dubyak, George R. Chen, Benjamin K. Front Immunol Immunology Human immunodeficiency virus type 1 (HIV-1) causes a chronic infection that afflicts more than 30 million individuals worldwide. While the infection can be suppressed with potent antiretroviral therapies, individuals infected with HIV-1 have elevated levels of inflammation as indicated by increased T cell activation, soluble biomarkers, and associated morbidity and mortality. A single mechanism linking HIV-1 pathogenesis to this inflammation has yet to be identified. Purinergic receptors are known to mediate inflammation and have been shown to be required for HIV-1 infection at the level of HIV-1 membrane fusion. Here, we review the literature on the role of purinergic receptors in HIV-1 infection and associated inflammation and describe a role for these receptors as potential therapeutic targets. Frontiers Media S.A. 2015-11-26 /pmc/articles/PMC4659914/ /pubmed/26635799 http://dx.doi.org/10.3389/fimmu.2015.00585 Text en Copyright © 2015 Swartz, Dubyak and Chen. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Swartz, Talia H.
Dubyak, George R.
Chen, Benjamin K.
Purinergic Receptors: Key Mediators of HIV-1 Infection and Inflammation
title Purinergic Receptors: Key Mediators of HIV-1 Infection and Inflammation
title_full Purinergic Receptors: Key Mediators of HIV-1 Infection and Inflammation
title_fullStr Purinergic Receptors: Key Mediators of HIV-1 Infection and Inflammation
title_full_unstemmed Purinergic Receptors: Key Mediators of HIV-1 Infection and Inflammation
title_short Purinergic Receptors: Key Mediators of HIV-1 Infection and Inflammation
title_sort purinergic receptors: key mediators of hiv-1 infection and inflammation
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4659914/
https://www.ncbi.nlm.nih.gov/pubmed/26635799
http://dx.doi.org/10.3389/fimmu.2015.00585
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