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Towards a small animal model for hepatitis C

Hepatitis C virus (HCV) causes chronic liver disease and affects an estimated 3% of the world's population. Options for the prevention or therapy of HCV infection are limited; there is no vaccine and the nonspecific, interferon-based treatments now in use are frequently ineffective and have sig...

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Detalles Bibliográficos
Autores principales: Ploss, Alexander, Rice, Charles M.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2775186/
https://www.ncbi.nlm.nih.gov/pubmed/19834510
http://dx.doi.org/10.1038/embor.2009.223
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author Ploss, Alexander
Rice, Charles M.
author_facet Ploss, Alexander
Rice, Charles M.
author_sort Ploss, Alexander
collection PubMed
description Hepatitis C virus (HCV) causes chronic liver disease and affects an estimated 3% of the world's population. Options for the prevention or therapy of HCV infection are limited; there is no vaccine and the nonspecific, interferon-based treatments now in use are frequently ineffective and have significant side effects. A small-animal model for HCV infection would significantly expedite antiviral compound development and preclinical testing, as well as open new avenues to decipher the mechanisms that underlie viral pathogenesis. The natural species tropism of HCV is, however, limited to humans and chimpanzees. Here, we discuss the prospects of developing a mouse model for HCV infection, taking into consideration recent results on HCV entry and replication, and new prospects in xenotransplantation biology. We highlight three independent, but possibly complementary, approaches towards overcoming current species barriers and generating a small-animal model for HCV pathogenesis.
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spelling pubmed-27751862010-11-01 Towards a small animal model for hepatitis C Ploss, Alexander Rice, Charles M. EMBO Rep Review Article Hepatitis C virus (HCV) causes chronic liver disease and affects an estimated 3% of the world's population. Options for the prevention or therapy of HCV infection are limited; there is no vaccine and the nonspecific, interferon-based treatments now in use are frequently ineffective and have significant side effects. A small-animal model for HCV infection would significantly expedite antiviral compound development and preclinical testing, as well as open new avenues to decipher the mechanisms that underlie viral pathogenesis. The natural species tropism of HCV is, however, limited to humans and chimpanzees. Here, we discuss the prospects of developing a mouse model for HCV infection, taking into consideration recent results on HCV entry and replication, and new prospects in xenotransplantation biology. We highlight three independent, but possibly complementary, approaches towards overcoming current species barriers and generating a small-animal model for HCV pathogenesis. Nature Publishing Group 2009-11 2009-10-16 /pmc/articles/PMC2775186/ /pubmed/19834510 http://dx.doi.org/10.1038/embor.2009.223 Text en Copyright © 2009, European Molecular Biology Organization
spellingShingle Review Article
Ploss, Alexander
Rice, Charles M.
Towards a small animal model for hepatitis C
title Towards a small animal model for hepatitis C
title_full Towards a small animal model for hepatitis C
title_fullStr Towards a small animal model for hepatitis C
title_full_unstemmed Towards a small animal model for hepatitis C
title_short Towards a small animal model for hepatitis C
title_sort towards a small animal model for hepatitis c
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2775186/
https://www.ncbi.nlm.nih.gov/pubmed/19834510
http://dx.doi.org/10.1038/embor.2009.223
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