Innate immunity modulation in virus entry

Entry into a cell submits viruses to detection by pattern recognition receptors (PRRs) leading to an early innate anti-viral response. Several viruses evolved strategies to avoid or subvert PRR recognition at the step of virus entry to promote infection. Whereas viruses mostly escape from soluble PR...

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Detalles Bibliográficos
Autores principales: Faure, Mathias, Rabourdin-Combe, Chantal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2011
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7102793/
https://www.ncbi.nlm.nih.gov/pubmed/22440562
http://dx.doi.org/10.1016/j.coviro.2011.05.013
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author Faure, Mathias
Rabourdin-Combe, Chantal
author_facet Faure, Mathias
Rabourdin-Combe, Chantal
author_sort Faure, Mathias
collection PubMed
description Entry into a cell submits viruses to detection by pattern recognition receptors (PRRs) leading to an early innate anti-viral response. Several viruses evolved strategies to avoid or subvert PRR recognition at the step of virus entry to promote infection. Whereas viruses mostly escape from soluble PRR detection, endocytic/phagocytic PRRs, such as the mannose receptor or DC-SIGN, are commonly used for virus entry. Moreover, virion-incorporated proteins may also offer viruses a way to dampen anti-viral innate immunity upon virus entry, and entering viruses might usurp autophagy to improve their own infectivity.
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spelling pubmed-71027932020-03-31 Innate immunity modulation in virus entry Faure, Mathias Rabourdin-Combe, Chantal Curr Opin Virol Article Entry into a cell submits viruses to detection by pattern recognition receptors (PRRs) leading to an early innate anti-viral response. Several viruses evolved strategies to avoid or subvert PRR recognition at the step of virus entry to promote infection. Whereas viruses mostly escape from soluble PRR detection, endocytic/phagocytic PRRs, such as the mannose receptor or DC-SIGN, are commonly used for virus entry. Moreover, virion-incorporated proteins may also offer viruses a way to dampen anti-viral innate immunity upon virus entry, and entering viruses might usurp autophagy to improve their own infectivity. Elsevier B.V. 2011-07 2011-06-20 /pmc/articles/PMC7102793/ /pubmed/22440562 http://dx.doi.org/10.1016/j.coviro.2011.05.013 Text en Copyright © 2011 Elsevier B.V. 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
Faure, Mathias
Rabourdin-Combe, Chantal
Innate immunity modulation in virus entry
title Innate immunity modulation in virus entry
title_full Innate immunity modulation in virus entry
title_fullStr Innate immunity modulation in virus entry
title_full_unstemmed Innate immunity modulation in virus entry
title_short Innate immunity modulation in virus entry
title_sort innate immunity modulation in virus entry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7102793/
https://www.ncbi.nlm.nih.gov/pubmed/22440562
http://dx.doi.org/10.1016/j.coviro.2011.05.013
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