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Update on Hepatitis C Virus and HIV Coinfection

Chronic hepatitis C virus (HCV) infection has historically been difficult to treat in the HIV-infected population, owing to generally poor responses to interferon-based therapies. The recent rapid development of directly acting antiviral agents (DAAs) against HCV has the potential to revolutionize t...

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Detalles Bibliográficos
Autores principales: Gemtessa, Tilahun Amdissa, Chirch, Lisa M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: XIA & HE Publishing Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4521281/
https://www.ncbi.nlm.nih.gov/pubmed/26355698
http://dx.doi.org/10.14218/JCTH.2013.00018
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author Gemtessa, Tilahun Amdissa
Chirch, Lisa M.
author_facet Gemtessa, Tilahun Amdissa
Chirch, Lisa M.
author_sort Gemtessa, Tilahun Amdissa
collection PubMed
description Chronic hepatitis C virus (HCV) infection has historically been difficult to treat in the HIV-infected population, owing to generally poor responses to interferon-based therapies. The recent rapid development of directly acting antiviral agents (DAAs) against HCV has the potential to revolutionize treatment of this infection in the HIV population by improving tolerability and outcome, and, ultimately, reducing the significant burden of liver-related morbidity and mortality in this population. Clinical trials to address the safety and efficacy of novel DAAs in the HCV/HIV coinfected population are ongoing, and show much promise. The rapidity of current drug discovery in the field of HCV is both impressive and daunting for clinicians who will have to master these drugs. Going forward, the inclusion of individuals from this large and growing patient population in clinical trials will be of paramount importance.
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spelling pubmed-45212812015-09-09 Update on Hepatitis C Virus and HIV Coinfection Gemtessa, Tilahun Amdissa Chirch, Lisa M. J Clin Transl Hepatol Review Article Chronic hepatitis C virus (HCV) infection has historically been difficult to treat in the HIV-infected population, owing to generally poor responses to interferon-based therapies. The recent rapid development of directly acting antiviral agents (DAAs) against HCV has the potential to revolutionize treatment of this infection in the HIV population by improving tolerability and outcome, and, ultimately, reducing the significant burden of liver-related morbidity and mortality in this population. Clinical trials to address the safety and efficacy of novel DAAs in the HCV/HIV coinfected population are ongoing, and show much promise. The rapidity of current drug discovery in the field of HCV is both impressive and daunting for clinicians who will have to master these drugs. Going forward, the inclusion of individuals from this large and growing patient population in clinical trials will be of paramount importance. XIA & HE Publishing Ltd 2013-12-15 2013-12 /pmc/articles/PMC4521281/ /pubmed/26355698 http://dx.doi.org/10.14218/JCTH.2013.00018 Text en © 2013 The Second Affiliated Hospital of Chongqing Medical University. Published by XIA & HE Publishing Ltd. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 4.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Gemtessa, Tilahun Amdissa
Chirch, Lisa M.
Update on Hepatitis C Virus and HIV Coinfection
title Update on Hepatitis C Virus and HIV Coinfection
title_full Update on Hepatitis C Virus and HIV Coinfection
title_fullStr Update on Hepatitis C Virus and HIV Coinfection
title_full_unstemmed Update on Hepatitis C Virus and HIV Coinfection
title_short Update on Hepatitis C Virus and HIV Coinfection
title_sort update on hepatitis c virus and hiv coinfection
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4521281/
https://www.ncbi.nlm.nih.gov/pubmed/26355698
http://dx.doi.org/10.14218/JCTH.2013.00018
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