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The interaction of HIV with dendritic cells: outcomes and pathways

Dendritic cells (DCs), including Langerhans Cells (LCs), are probably among the earliest targets of HIV infection. Their localization in mucosal epithelia and in the T cell areas of lymphoid organs, as well as their crucial role in capturing antigens and initiating T cell responses, highlight their...

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Detalles Bibliográficos
Autores principales: Piguet, Vincent, Steinman, Ralph M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106400/
https://www.ncbi.nlm.nih.gov/pubmed/17950666
http://dx.doi.org/10.1016/j.it.2007.07.010
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author Piguet, Vincent
Steinman, Ralph M.
author_facet Piguet, Vincent
Steinman, Ralph M.
author_sort Piguet, Vincent
collection PubMed
description Dendritic cells (DCs), including Langerhans Cells (LCs), are probably among the earliest targets of HIV infection. Their localization in mucosal epithelia and in the T cell areas of lymphoid organs, as well as their crucial role in capturing antigens and initiating T cell responses, highlight their potential importance. Studies with cells in culture have addressed different outcomes of the HIV-–DC interaction, which include: direct productive infection of DC; carriage of virus by DC to CD4(+) T cells; transfer of virus between DC and T cells at an infectious synapse; and immune evasion strategies of infected DC. Here we review the literature covering these areas, including current knowledge of underlying mechanisms or pathways.
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spelling pubmed-71064002020-03-31 The interaction of HIV with dendritic cells: outcomes and pathways Piguet, Vincent Steinman, Ralph M. Trends Immunol Article Dendritic cells (DCs), including Langerhans Cells (LCs), are probably among the earliest targets of HIV infection. Their localization in mucosal epithelia and in the T cell areas of lymphoid organs, as well as their crucial role in capturing antigens and initiating T cell responses, highlight their potential importance. Studies with cells in culture have addressed different outcomes of the HIV-–DC interaction, which include: direct productive infection of DC; carriage of virus by DC to CD4(+) T cells; transfer of virus between DC and T cells at an infectious synapse; and immune evasion strategies of infected DC. Here we review the literature covering these areas, including current knowledge of underlying mechanisms or pathways. Elsevier Ltd. 2007-11 2007-10-23 /pmc/articles/PMC7106400/ /pubmed/17950666 http://dx.doi.org/10.1016/j.it.2007.07.010 Text en Copyright © 2007 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Piguet, Vincent
Steinman, Ralph M.
The interaction of HIV with dendritic cells: outcomes and pathways
title The interaction of HIV with dendritic cells: outcomes and pathways
title_full The interaction of HIV with dendritic cells: outcomes and pathways
title_fullStr The interaction of HIV with dendritic cells: outcomes and pathways
title_full_unstemmed The interaction of HIV with dendritic cells: outcomes and pathways
title_short The interaction of HIV with dendritic cells: outcomes and pathways
title_sort interaction of hiv with dendritic cells: outcomes and pathways
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106400/
https://www.ncbi.nlm.nih.gov/pubmed/17950666
http://dx.doi.org/10.1016/j.it.2007.07.010
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