Future Directions in the Treatment of Patients with Chronic Hepatitis C Virus Infection

Hepatitis C virus (HCV) infects over 170 million people worldwide. While interferon is currently the most used single agent therapy, this drug may result in a sustained loss of virus from the blood in only up to 15% of patients; new options for treatment are needed. With the release of ribavirin in...

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Main Author: Robert G Gish
Format: Article
Language:English
Published: Hindawi Limited 1999-01-01
Series:Canadian Journal of Gastroenterology
Online Access:http://dx.doi.org/10.1155/1999/309272
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spelling doaj-f580b81265cd47869d7084496a823bfd2020-11-24T21:09:30ZengHindawi LimitedCanadian Journal of Gastroenterology0835-79001999-01-01131576210.1155/1999/309272Future Directions in the Treatment of Patients with Chronic Hepatitis C Virus InfectionRobert G Gish0Departments of Medicine and Transplantation, California Pacific Medical Center, San Francisco, USAHepatitis C virus (HCV) infects over 170 million people worldwide. While interferon is currently the most used single agent therapy, this drug may result in a sustained loss of virus from the blood in only up to 15% of patients; new options for treatment are needed. With the release of ribavirin in North America and Europe, a viral clearance rate or ‘cure’ may be attained in up to 40% of patients. Developing successful antiviral therapy that prevents or delays the development of cirrhosis, liver failure and liver cancer as well as decreasing the demand for liver transplantation are clearly identified goals. Unfortunately, there is no complete in vitro model of HCV replication or translation. Due to the lack of an animal or cell culture model of HCV infection, in vitro translation screening systems to identify inhibitors of HCV protein translation are being evaluated by a large number of biotechnology companies. With advancing computer technology, high throughput screening processes are now possible and can be joined to specific in vitro model testing systems. Along with examining some of the information known about HCV therapy and the HCV genome, the present review discusses potential targets for new therapies and identifies therapeutic agents that are nearing clinical applicationhttp://dx.doi.org/10.1155/1999/309272
collection DOAJ
language English
format Article
sources DOAJ
author Robert G Gish
spellingShingle Robert G Gish
Future Directions in the Treatment of Patients with Chronic Hepatitis C Virus Infection
Canadian Journal of Gastroenterology
author_facet Robert G Gish
author_sort Robert G Gish
title Future Directions in the Treatment of Patients with Chronic Hepatitis C Virus Infection
title_short Future Directions in the Treatment of Patients with Chronic Hepatitis C Virus Infection
title_full Future Directions in the Treatment of Patients with Chronic Hepatitis C Virus Infection
title_fullStr Future Directions in the Treatment of Patients with Chronic Hepatitis C Virus Infection
title_full_unstemmed Future Directions in the Treatment of Patients with Chronic Hepatitis C Virus Infection
title_sort future directions in the treatment of patients with chronic hepatitis c virus infection
publisher Hindawi Limited
series Canadian Journal of Gastroenterology
issn 0835-7900
publishDate 1999-01-01
description Hepatitis C virus (HCV) infects over 170 million people worldwide. While interferon is currently the most used single agent therapy, this drug may result in a sustained loss of virus from the blood in only up to 15% of patients; new options for treatment are needed. With the release of ribavirin in North America and Europe, a viral clearance rate or ‘cure’ may be attained in up to 40% of patients. Developing successful antiviral therapy that prevents or delays the development of cirrhosis, liver failure and liver cancer as well as decreasing the demand for liver transplantation are clearly identified goals. Unfortunately, there is no complete in vitro model of HCV replication or translation. Due to the lack of an animal or cell culture model of HCV infection, in vitro translation screening systems to identify inhibitors of HCV protein translation are being evaluated by a large number of biotechnology companies. With advancing computer technology, high throughput screening processes are now possible and can be joined to specific in vitro model testing systems. Along with examining some of the information known about HCV therapy and the HCV genome, the present review discusses potential targets for new therapies and identifies therapeutic agents that are nearing clinical application
url http://dx.doi.org/10.1155/1999/309272
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