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T-Cell Signaling in HIV-1 Infection

HIV exploits the T-cell signaling network to gain access to downstream cellular components, which serves as effective tools to break the cellular barriers. Multiple host factors and their interaction with viral proteins contribute to the complexity of HIV-1 pathogenesis and disease progression. HIV-...

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Detalles Bibliográficos
Autores principales: Abbas, Wasim, Herbein, Georges
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Open 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751038/
https://www.ncbi.nlm.nih.gov/pubmed/23986795
http://dx.doi.org/10.2174/1874357920130621001
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author Abbas, Wasim
Herbein, Georges
author_facet Abbas, Wasim
Herbein, Georges
author_sort Abbas, Wasim
collection PubMed
description HIV exploits the T-cell signaling network to gain access to downstream cellular components, which serves as effective tools to break the cellular barriers. Multiple host factors and their interaction with viral proteins contribute to the complexity of HIV-1 pathogenesis and disease progression. HIV-1 proteins gp120, Nef, Tat and Vpr alter the T-cell signaling pathways by activating multiple transcription factors including NF-ĸB, Sp1 and AP-1. HIV-1 evades the immune system by developing a multi-pronged strategy. Additionally, HIV-1 encoded proteins influence the apoptosis in the host cell favoring or blocking T-cell apoptosis. Thus, T-cell signaling hijacked by viral proteins accounts for both viral persistence and immune suppression during HIV-1 infection. Here, we summarize past and present studies on HIV-1 T-cell signaling with special focus on the possible role of T cells in facilitating viral infection and pathogenesis
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spelling pubmed-37510382013-08-28 T-Cell Signaling in HIV-1 Infection Abbas, Wasim Herbein, Georges Open Virol J Article HIV exploits the T-cell signaling network to gain access to downstream cellular components, which serves as effective tools to break the cellular barriers. Multiple host factors and their interaction with viral proteins contribute to the complexity of HIV-1 pathogenesis and disease progression. HIV-1 proteins gp120, Nef, Tat and Vpr alter the T-cell signaling pathways by activating multiple transcription factors including NF-ĸB, Sp1 and AP-1. HIV-1 evades the immune system by developing a multi-pronged strategy. Additionally, HIV-1 encoded proteins influence the apoptosis in the host cell favoring or blocking T-cell apoptosis. Thus, T-cell signaling hijacked by viral proteins accounts for both viral persistence and immune suppression during HIV-1 infection. Here, we summarize past and present studies on HIV-1 T-cell signaling with special focus on the possible role of T cells in facilitating viral infection and pathogenesis Bentham Open 2013-07-26 /pmc/articles/PMC3751038/ /pubmed/23986795 http://dx.doi.org/10.2174/1874357920130621001 Text en © Abbas and Herbein; Licensee Bentham Open. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Abbas, Wasim
Herbein, Georges
T-Cell Signaling in HIV-1 Infection
title T-Cell Signaling in HIV-1 Infection
title_full T-Cell Signaling in HIV-1 Infection
title_fullStr T-Cell Signaling in HIV-1 Infection
title_full_unstemmed T-Cell Signaling in HIV-1 Infection
title_short T-Cell Signaling in HIV-1 Infection
title_sort t-cell signaling in hiv-1 infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751038/
https://www.ncbi.nlm.nih.gov/pubmed/23986795
http://dx.doi.org/10.2174/1874357920130621001
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