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The Natural Killer Cell Response to HCV Infection

In the last few years major progress has been made in better understanding the role of natural killer (NK) cells in hepatitis C virus (HCV) infection. This includes multiple pathways by which HCV impairs or limits NK cells activation. Based on current genetic and functional data, a picture is emergi...

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Autor principal: Ahlenstiel, Golo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Association of Immunologists 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817297/
https://www.ncbi.nlm.nih.gov/pubmed/24198741
http://dx.doi.org/10.4110/in.2013.13.5.168
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author Ahlenstiel, Golo
author_facet Ahlenstiel, Golo
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description In the last few years major progress has been made in better understanding the role of natural killer (NK) cells in hepatitis C virus (HCV) infection. This includes multiple pathways by which HCV impairs or limits NK cells activation. Based on current genetic and functional data, a picture is emerging where only a rapid and strong NK cell response early on during infection which results in strong T cell responses and possible subsequent clearance, whereas chronic HCV infection is associated with dysfunctional or biased NK cells phenotypes. The hallmark of this NK cell dysfunction is persistent activation promoting ongoing hepatitis and hepatocyte damage, while being unable to clear HCV due to impaired IFN-γ responses. Furthermore, some data suggests certain chronically activated subsets that are NKp46(high) may be particularly active against hepatic stellate cells, a key player in hepatic fibrogenesis. Finally, the role of NK cells during HCV therapy, HCV recurrence after liver transplant and hepatocellular carcinoma are discussed.
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spelling pubmed-38172972013-11-06 The Natural Killer Cell Response to HCV Infection Ahlenstiel, Golo Immune Netw Review Article In the last few years major progress has been made in better understanding the role of natural killer (NK) cells in hepatitis C virus (HCV) infection. This includes multiple pathways by which HCV impairs or limits NK cells activation. Based on current genetic and functional data, a picture is emerging where only a rapid and strong NK cell response early on during infection which results in strong T cell responses and possible subsequent clearance, whereas chronic HCV infection is associated with dysfunctional or biased NK cells phenotypes. The hallmark of this NK cell dysfunction is persistent activation promoting ongoing hepatitis and hepatocyte damage, while being unable to clear HCV due to impaired IFN-γ responses. Furthermore, some data suggests certain chronically activated subsets that are NKp46(high) may be particularly active against hepatic stellate cells, a key player in hepatic fibrogenesis. Finally, the role of NK cells during HCV therapy, HCV recurrence after liver transplant and hepatocellular carcinoma are discussed. The Korean Association of Immunologists 2013-10 2013-10-26 /pmc/articles/PMC3817297/ /pubmed/24198741 http://dx.doi.org/10.4110/in.2013.13.5.168 Text en Copyright © 2013 The Korean Association of Immunologists http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Ahlenstiel, Golo
The Natural Killer Cell Response to HCV Infection
title The Natural Killer Cell Response to HCV Infection
title_full The Natural Killer Cell Response to HCV Infection
title_fullStr The Natural Killer Cell Response to HCV Infection
title_full_unstemmed The Natural Killer Cell Response to HCV Infection
title_short The Natural Killer Cell Response to HCV Infection
title_sort natural killer cell response to hcv infection
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817297/
https://www.ncbi.nlm.nih.gov/pubmed/24198741
http://dx.doi.org/10.4110/in.2013.13.5.168
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