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Antiviral Properties of ISG15

The type I interferon system plays a critical role in limiting the spread of viral infection. Viruses induce the production of interferon (IFN), which after binding to the IFN-α/β receptor (IFNAR), and triggering of the JAK/STAT signaling cascade, results in the induction of interferon-stimulated ge...

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Autor principal: Lenschow, Deborah J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185569/
https://www.ncbi.nlm.nih.gov/pubmed/21994614
http://dx.doi.org/10.3390/v2102154
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author Lenschow, Deborah J.
author_facet Lenschow, Deborah J.
author_sort Lenschow, Deborah J.
collection PubMed
description The type I interferon system plays a critical role in limiting the spread of viral infection. Viruses induce the production of interferon (IFN), which after binding to the IFN-α/β receptor (IFNAR), and triggering of the JAK/STAT signaling cascade, results in the induction of interferon-stimulated genes (ISGs). These ISGs function to inhibit viral replication and to regulate the host immune response. Among these ISGs, the ubiquitin-like molecule, ISG15, is one of the most strongly induced proteins. Similar to ubiquitin, through an IFN induced conjugation cascade, ISG15 is covalently linked to a variety of cellular proteins, suggesting regulation of different cellular processes. Studies performed over the past several years have shown that ISG15 plays a central role in the host’s antiviral response against many viruses. Mice lacking ISG15 display increased susceptibility to multiple viruses. Furthermore, several viruses have developed immune evasion strategies that directly target the ISG15 pathway. Work is now underway to determine the mechanism by which ISG15 functions as an antiviral molecule, such that therapies targeting this pathway can be developed in the future.
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spelling pubmed-31855692011-10-12 Antiviral Properties of ISG15 Lenschow, Deborah J. Viruses Review The type I interferon system plays a critical role in limiting the spread of viral infection. Viruses induce the production of interferon (IFN), which after binding to the IFN-α/β receptor (IFNAR), and triggering of the JAK/STAT signaling cascade, results in the induction of interferon-stimulated genes (ISGs). These ISGs function to inhibit viral replication and to regulate the host immune response. Among these ISGs, the ubiquitin-like molecule, ISG15, is one of the most strongly induced proteins. Similar to ubiquitin, through an IFN induced conjugation cascade, ISG15 is covalently linked to a variety of cellular proteins, suggesting regulation of different cellular processes. Studies performed over the past several years have shown that ISG15 plays a central role in the host’s antiviral response against many viruses. Mice lacking ISG15 display increased susceptibility to multiple viruses. Furthermore, several viruses have developed immune evasion strategies that directly target the ISG15 pathway. Work is now underway to determine the mechanism by which ISG15 functions as an antiviral molecule, such that therapies targeting this pathway can be developed in the future. Molecular Diversity Preservation International (MDPI) 2010-09-28 /pmc/articles/PMC3185569/ /pubmed/21994614 http://dx.doi.org/10.3390/v2102154 Text en © 2010 by the authors; licensee MDPI, 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
Lenschow, Deborah J.
Antiviral Properties of ISG15
title Antiviral Properties of ISG15
title_full Antiviral Properties of ISG15
title_fullStr Antiviral Properties of ISG15
title_full_unstemmed Antiviral Properties of ISG15
title_short Antiviral Properties of ISG15
title_sort antiviral properties of isg15
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185569/
https://www.ncbi.nlm.nih.gov/pubmed/21994614
http://dx.doi.org/10.3390/v2102154
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