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Plasmacytoid Dendritic Cells and the Control of Herpesvirus Infections

Type-I interferons (IFN-I) are cytokines essential for vertebrate antiviral defense, including against herpesviruses. IFN-I have potent direct antiviral activities and also mediate a multiplicity of immunoregulatory functions, which can either promote or dampen antiviral adaptive immune responses. P...

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Detalles Bibliográficos
Autores principales: Baranek, Thomas, Zucchini, Nicolas, Dalod, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185500/
https://www.ncbi.nlm.nih.gov/pubmed/21994554
http://dx.doi.org/10.3390/v1030383
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author Baranek, Thomas
Zucchini, Nicolas
Dalod, Marc
author_facet Baranek, Thomas
Zucchini, Nicolas
Dalod, Marc
author_sort Baranek, Thomas
collection PubMed
description Type-I interferons (IFN-I) are cytokines essential for vertebrate antiviral defense, including against herpesviruses. IFN-I have potent direct antiviral activities and also mediate a multiplicity of immunoregulatory functions, which can either promote or dampen antiviral adaptive immune responses. Plasmacytoid dendritic cells (pDCs) are the professional producers of IFN-I in response to many viruses, including all of the herpesviruses tested. There is strong evidence that pDCs could play a major role in the initial orchestration of both innate and adaptive antiviral immune responses. Depending on their activation pattern, pDC responses may be either protective or detrimental to the host. Here, we summarize and discuss current knowledge regarding pDC implication in the physiopathology of mouse and human herpesvirus infections, and we discuss how pDC functions could be manipulated in immunotherapeutic settings to promote health over disease.
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spelling pubmed-31855002011-10-12 Plasmacytoid Dendritic Cells and the Control of Herpesvirus Infections Baranek, Thomas Zucchini, Nicolas Dalod, Marc Viruses Review Type-I interferons (IFN-I) are cytokines essential for vertebrate antiviral defense, including against herpesviruses. IFN-I have potent direct antiviral activities and also mediate a multiplicity of immunoregulatory functions, which can either promote or dampen antiviral adaptive immune responses. Plasmacytoid dendritic cells (pDCs) are the professional producers of IFN-I in response to many viruses, including all of the herpesviruses tested. There is strong evidence that pDCs could play a major role in the initial orchestration of both innate and adaptive antiviral immune responses. Depending on their activation pattern, pDC responses may be either protective or detrimental to the host. Here, we summarize and discuss current knowledge regarding pDC implication in the physiopathology of mouse and human herpesvirus infections, and we discuss how pDC functions could be manipulated in immunotherapeutic settings to promote health over disease. Molecular Diversity Preservation International (MDPI) 2009-10-14 /pmc/articles/PMC3185500/ /pubmed/21994554 http://dx.doi.org/10.3390/v1030383 Text en © 2009 by the authors; licensee Molecular Diversity Preservation International, 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
Baranek, Thomas
Zucchini, Nicolas
Dalod, Marc
Plasmacytoid Dendritic Cells and the Control of Herpesvirus Infections
title Plasmacytoid Dendritic Cells and the Control of Herpesvirus Infections
title_full Plasmacytoid Dendritic Cells and the Control of Herpesvirus Infections
title_fullStr Plasmacytoid Dendritic Cells and the Control of Herpesvirus Infections
title_full_unstemmed Plasmacytoid Dendritic Cells and the Control of Herpesvirus Infections
title_short Plasmacytoid Dendritic Cells and the Control of Herpesvirus Infections
title_sort plasmacytoid dendritic cells and the control of herpesvirus infections
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185500/
https://www.ncbi.nlm.nih.gov/pubmed/21994554
http://dx.doi.org/10.3390/v1030383
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