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Direct Antiviral Mechanisms of Interferon-Gamma

Interferon-gamma (IFNG) is a pleiotropic cytokine that modulates both innate and adaptive immune networks; it is the most potent activator of macrophages and a signature cytokine of activated T lymphocytes. Though IFNG is now appreciated to have a multitude of roles in immune modulation and broad-sp...

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Autores principales: Kang, Soowon, Brown, Hailey M., Hwang, Seungmin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Association of Immunologists 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6215902/
https://www.ncbi.nlm.nih.gov/pubmed/30402328
http://dx.doi.org/10.4110/in.2018.18.e33
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author Kang, Soowon
Brown, Hailey M.
Hwang, Seungmin
author_facet Kang, Soowon
Brown, Hailey M.
Hwang, Seungmin
author_sort Kang, Soowon
collection PubMed
description Interferon-gamma (IFNG) is a pleiotropic cytokine that modulates both innate and adaptive immune networks; it is the most potent activator of macrophages and a signature cytokine of activated T lymphocytes. Though IFNG is now appreciated to have a multitude of roles in immune modulation and broad-spectrum pathogen defense, it was originally discovered, and named, as a secretory factor that interferes with viral replication. In contrast to the prototypical type I interferons produced by any cells upon viral infection, only specific subsets of immune cells can produce IFNG upon infection or stimulation with antigen or mitogen. Still, virtually all cells can respond to both types of interferons. This makes IFNG a versatile anti-microbial cytokine and also gives it a unique position in the antiviral defense system. The goal of this review is to highlight the direct antiviral mechanisms of IFNG, thereby clarifying its antiviral function in the effective control of viral infections.
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spelling pubmed-62159022018-11-06 Direct Antiviral Mechanisms of Interferon-Gamma Kang, Soowon Brown, Hailey M. Hwang, Seungmin Immune Netw Review Article Interferon-gamma (IFNG) is a pleiotropic cytokine that modulates both innate and adaptive immune networks; it is the most potent activator of macrophages and a signature cytokine of activated T lymphocytes. Though IFNG is now appreciated to have a multitude of roles in immune modulation and broad-spectrum pathogen defense, it was originally discovered, and named, as a secretory factor that interferes with viral replication. In contrast to the prototypical type I interferons produced by any cells upon viral infection, only specific subsets of immune cells can produce IFNG upon infection or stimulation with antigen or mitogen. Still, virtually all cells can respond to both types of interferons. This makes IFNG a versatile anti-microbial cytokine and also gives it a unique position in the antiviral defense system. The goal of this review is to highlight the direct antiviral mechanisms of IFNG, thereby clarifying its antiviral function in the effective control of viral infections. The Korean Association of Immunologists 2018-10-17 /pmc/articles/PMC6215902/ /pubmed/30402328 http://dx.doi.org/10.4110/in.2018.18.e33 Text en Copyright © 2018. The Korean Association of Immunologists https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Kang, Soowon
Brown, Hailey M.
Hwang, Seungmin
Direct Antiviral Mechanisms of Interferon-Gamma
title Direct Antiviral Mechanisms of Interferon-Gamma
title_full Direct Antiviral Mechanisms of Interferon-Gamma
title_fullStr Direct Antiviral Mechanisms of Interferon-Gamma
title_full_unstemmed Direct Antiviral Mechanisms of Interferon-Gamma
title_short Direct Antiviral Mechanisms of Interferon-Gamma
title_sort direct antiviral mechanisms of interferon-gamma
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6215902/
https://www.ncbi.nlm.nih.gov/pubmed/30402328
http://dx.doi.org/10.4110/in.2018.18.e33
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