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Hepatitis E Virus Drug Development

Hepatitis E virus (HEV) is an underestimated disease, leading to estimated 20 million infections and up to 70,000 deaths annually. Infections are mostly asymptomatic but can reach mortality rates up to 25% in pregnant women or become chronic in immunocompromised patients. The current therapy options...

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Detalles Bibliográficos
Autores principales: Kinast, Volker, Burkard, Thomas L, Todt, Daniel, Steinmann, Eike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6631701/
https://www.ncbi.nlm.nih.gov/pubmed/31141919
http://dx.doi.org/10.3390/v11060485
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author Kinast, Volker
Burkard, Thomas L
Todt, Daniel
Steinmann, Eike
author_facet Kinast, Volker
Burkard, Thomas L
Todt, Daniel
Steinmann, Eike
author_sort Kinast, Volker
collection PubMed
description Hepatitis E virus (HEV) is an underestimated disease, leading to estimated 20 million infections and up to 70,000 deaths annually. Infections are mostly asymptomatic but can reach mortality rates up to 25% in pregnant women or become chronic in immunocompromised patients. The current therapy options are limited to the unspecific antivirals Ribavirin (RBV) and pegylated Interferon-α (pegIFN-α). RBV leads to viral clearance in only 80% of patients treated, and is, similar to pegIFN-α, contraindicated in the major risk group of pregnant women, emphasizing the importance of new therapy options. In this review, we focus on the urgent need and current efforts in HEV drug development. We provide an overview of the current status of HEV antiviral research. Furthermore, we discuss strategies for drug development and the limitations of the approaches with respect to HEV.
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spelling pubmed-66317012019-08-19 Hepatitis E Virus Drug Development Kinast, Volker Burkard, Thomas L Todt, Daniel Steinmann, Eike Viruses Review Hepatitis E virus (HEV) is an underestimated disease, leading to estimated 20 million infections and up to 70,000 deaths annually. Infections are mostly asymptomatic but can reach mortality rates up to 25% in pregnant women or become chronic in immunocompromised patients. The current therapy options are limited to the unspecific antivirals Ribavirin (RBV) and pegylated Interferon-α (pegIFN-α). RBV leads to viral clearance in only 80% of patients treated, and is, similar to pegIFN-α, contraindicated in the major risk group of pregnant women, emphasizing the importance of new therapy options. In this review, we focus on the urgent need and current efforts in HEV drug development. We provide an overview of the current status of HEV antiviral research. Furthermore, we discuss strategies for drug development and the limitations of the approaches with respect to HEV. MDPI 2019-05-28 /pmc/articles/PMC6631701/ /pubmed/31141919 http://dx.doi.org/10.3390/v11060485 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
Kinast, Volker
Burkard, Thomas L
Todt, Daniel
Steinmann, Eike
Hepatitis E Virus Drug Development
title Hepatitis E Virus Drug Development
title_full Hepatitis E Virus Drug Development
title_fullStr Hepatitis E Virus Drug Development
title_full_unstemmed Hepatitis E Virus Drug Development
title_short Hepatitis E Virus Drug Development
title_sort hepatitis e virus drug development
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6631701/
https://www.ncbi.nlm.nih.gov/pubmed/31141919
http://dx.doi.org/10.3390/v11060485
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