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The Good and the Bad of Natural Killer Cells in Virus Control: Perspective for Anti-HBV Therapy

Immune modulatory therapies are widely believed to represent potential therapeutic strategies for chronic hepatitis B infection (CHB). Among the cellular targets for immune interventions, Natural Killer (NK) cells represent possible candidates because they have a key role in anti-viral control by pr...

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Autores principales: Fisicaro, Paola, Rossi, Marzia, Vecchi, Andrea, Acerbi, Greta, Barili, Valeria, Laccabue, Diletta, Montali, Ilaria, Zecca, Alessandra, Penna, Amalia, Missale, Gabriele, Ferrari, Carlo, Boni, Carolina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6834135/
https://www.ncbi.nlm.nih.gov/pubmed/31614928
http://dx.doi.org/10.3390/ijms20205080
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author Fisicaro, Paola
Rossi, Marzia
Vecchi, Andrea
Acerbi, Greta
Barili, Valeria
Laccabue, Diletta
Montali, Ilaria
Zecca, Alessandra
Penna, Amalia
Missale, Gabriele
Ferrari, Carlo
Boni, Carolina
author_facet Fisicaro, Paola
Rossi, Marzia
Vecchi, Andrea
Acerbi, Greta
Barili, Valeria
Laccabue, Diletta
Montali, Ilaria
Zecca, Alessandra
Penna, Amalia
Missale, Gabriele
Ferrari, Carlo
Boni, Carolina
author_sort Fisicaro, Paola
collection PubMed
description Immune modulatory therapies are widely believed to represent potential therapeutic strategies for chronic hepatitis B infection (CHB). Among the cellular targets for immune interventions, Natural Killer (NK) cells represent possible candidates because they have a key role in anti-viral control by producing cytokines and by exerting cytotoxic functions against virus-infected cells. However, in patients with chronic hepatitis B, NK cells have been described to be more pathogenic than protective with preserved cytolytic activity but with a poor capacity to produce anti-viral cytokines. In addition, NK cells can exert a regulatory activity and possibly suppress adaptive immune responses in the setting of persistent viral infections. Consequently, a potential drawback of NK-cell targeted modulatory interventions is that they can potentiate the suppressive NK cell effect on virus-specific T cells, which further causes impairment of exhausted anti-viral T cell functions. Thus, clinically useful NK-cell modulatory strategies should be not only suited to improve positive anti-viral NK cell functions but also to abrogate T cell suppression by NK cell-mediated T cell killing. This review outlines the main NK cell features with a particular focus on CHB infection. It describes different mechanisms involved in NK-T cell interplay as well as how NK cells can have positive anti-viral effector functions and negative suppressive effects on T cells activity. This review discusses how modulation of their balance can have potential therapeutic implications.
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spelling pubmed-68341352019-11-25 The Good and the Bad of Natural Killer Cells in Virus Control: Perspective for Anti-HBV Therapy Fisicaro, Paola Rossi, Marzia Vecchi, Andrea Acerbi, Greta Barili, Valeria Laccabue, Diletta Montali, Ilaria Zecca, Alessandra Penna, Amalia Missale, Gabriele Ferrari, Carlo Boni, Carolina Int J Mol Sci Review Immune modulatory therapies are widely believed to represent potential therapeutic strategies for chronic hepatitis B infection (CHB). Among the cellular targets for immune interventions, Natural Killer (NK) cells represent possible candidates because they have a key role in anti-viral control by producing cytokines and by exerting cytotoxic functions against virus-infected cells. However, in patients with chronic hepatitis B, NK cells have been described to be more pathogenic than protective with preserved cytolytic activity but with a poor capacity to produce anti-viral cytokines. In addition, NK cells can exert a regulatory activity and possibly suppress adaptive immune responses in the setting of persistent viral infections. Consequently, a potential drawback of NK-cell targeted modulatory interventions is that they can potentiate the suppressive NK cell effect on virus-specific T cells, which further causes impairment of exhausted anti-viral T cell functions. Thus, clinically useful NK-cell modulatory strategies should be not only suited to improve positive anti-viral NK cell functions but also to abrogate T cell suppression by NK cell-mediated T cell killing. This review outlines the main NK cell features with a particular focus on CHB infection. It describes different mechanisms involved in NK-T cell interplay as well as how NK cells can have positive anti-viral effector functions and negative suppressive effects on T cells activity. This review discusses how modulation of their balance can have potential therapeutic implications. MDPI 2019-10-13 /pmc/articles/PMC6834135/ /pubmed/31614928 http://dx.doi.org/10.3390/ijms20205080 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Fisicaro, Paola
Rossi, Marzia
Vecchi, Andrea
Acerbi, Greta
Barili, Valeria
Laccabue, Diletta
Montali, Ilaria
Zecca, Alessandra
Penna, Amalia
Missale, Gabriele
Ferrari, Carlo
Boni, Carolina
The Good and the Bad of Natural Killer Cells in Virus Control: Perspective for Anti-HBV Therapy
title The Good and the Bad of Natural Killer Cells in Virus Control: Perspective for Anti-HBV Therapy
title_full The Good and the Bad of Natural Killer Cells in Virus Control: Perspective for Anti-HBV Therapy
title_fullStr The Good and the Bad of Natural Killer Cells in Virus Control: Perspective for Anti-HBV Therapy
title_full_unstemmed The Good and the Bad of Natural Killer Cells in Virus Control: Perspective for Anti-HBV Therapy
title_short The Good and the Bad of Natural Killer Cells in Virus Control: Perspective for Anti-HBV Therapy
title_sort good and the bad of natural killer cells in virus control: perspective for anti-hbv therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6834135/
https://www.ncbi.nlm.nih.gov/pubmed/31614928
http://dx.doi.org/10.3390/ijms20205080
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