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Immune Responses to Viruses in the CNS

For recovery from infection, the immune response in the central nervous system (CNS) must eliminate or control virus replication without destroying nonrenewable, essential cells. Thus, upon intracellular virus detection, the infected cell must initiate clearance pathways without triggering neuronal...

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Detalles Bibliográficos
Autores principales: Schultz, Kimberly L.W., Griffin, Diane E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7151986/
http://dx.doi.org/10.1016/B978-0-12-374279-7.14022-6
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author Schultz, Kimberly L.W.
Griffin, Diane E.
author_facet Schultz, Kimberly L.W.
Griffin, Diane E.
author_sort Schultz, Kimberly L.W.
collection PubMed
description For recovery from infection, the immune response in the central nervous system (CNS) must eliminate or control virus replication without destroying nonrenewable, essential cells. Thus, upon intracellular virus detection, the infected cell must initiate clearance pathways without triggering neuronal cell death. As a result, the inflammatory response must be tightly regulated and unique mechanisms contribute to the immune response in the CNS. Early restriction of virus replication is accomplished by the innate immune response upon activation of pattern recognition receptors in resident cells. Infiltrating immune cells enter from the periphery to clear virus. Antibodies and interferon-γ are primary contributors to noncytolytic clearance of virus in the CNS. Lymphocytes are retained in the CNS after the acute phase of infection presumably to block reactivation of virus replication.
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spelling pubmed-71519862020-04-13 Immune Responses to Viruses in the CNS Schultz, Kimberly L.W. Griffin, Diane E. Encyclopedia of Immunobiology Article For recovery from infection, the immune response in the central nervous system (CNS) must eliminate or control virus replication without destroying nonrenewable, essential cells. Thus, upon intracellular virus detection, the infected cell must initiate clearance pathways without triggering neuronal cell death. As a result, the inflammatory response must be tightly regulated and unique mechanisms contribute to the immune response in the CNS. Early restriction of virus replication is accomplished by the innate immune response upon activation of pattern recognition receptors in resident cells. Infiltrating immune cells enter from the periphery to clear virus. Antibodies and interferon-γ are primary contributors to noncytolytic clearance of virus in the CNS. Lymphocytes are retained in the CNS after the acute phase of infection presumably to block reactivation of virus replication. 2016 2016-05-09 /pmc/articles/PMC7151986/ http://dx.doi.org/10.1016/B978-0-12-374279-7.14022-6 Text en Copyright © 2016 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
Schultz, Kimberly L.W.
Griffin, Diane E.
Immune Responses to Viruses in the CNS
title Immune Responses to Viruses in the CNS
title_full Immune Responses to Viruses in the CNS
title_fullStr Immune Responses to Viruses in the CNS
title_full_unstemmed Immune Responses to Viruses in the CNS
title_short Immune Responses to Viruses in the CNS
title_sort immune responses to viruses in the cns
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7151986/
http://dx.doi.org/10.1016/B978-0-12-374279-7.14022-6
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