From HCV To HBV Cure
- PMID: 28052627
- PMCID: PMC5217293
- DOI: 10.1111/liv.13324
From HCV To HBV Cure
Abstract
Approximately 170 million people are chronically infected with HCV and 350 million are chronically infected with HBV worldwide. It is estimated that more than one million patients die from complications related to chronic viral hepatitis, mainly HCC which is one of the most frequent cancers in many countries, especially Africa, the Middle East and Asia. HCV drug development has been impressive, and this revolution led to several direct-acting antiviral agents achieving an HCV cure after only 6-12 weeks. This progress could theorically lead to HCV global elimination making HCV and its consequences a rarity. HBV research and development programs can learn from the HCV experience, to achieve an HBV functional or sterilizing cure. This review will summarize key steps which have been realized for an HCV cure, and discuss the next steps to achieve for an HCV elimination. And also, how this HCV revolution has inspired scientists and clinicians to achieve the same for HBV.
Keywords: HBV cure; HCV elimination; capsid inhibitors; cccDNA; direct-acting antivirals.
© 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
Conflict of interest statement
Raymond Schinazi is the founder and major shareholder of Cocrystal Pharma, Inc. Tarik Asselah is a speaker and investigator for Abbvie, BMS, Boehringer-Ingelheim, Tibotec, Janssen, Gilead, Roche and MSD
References
-
- Choo QL, Kuo G, Weiner AJ, et al. Isolation of a cDNA clone derived from a blood-borne non-A, non-B viral hepatitis genome. Science. 1989;244:359–62. - PubMed
-
- Lohmann V, Korner F, Koch J, et al. Replication of sub- genomic hepatitis C virus RNAs in a hepatoma cell line. Science. 1999;285:110–3. - PubMed
-
- Blight KJ, Kolykhalov AA, Rice CM. Efficient initiation of HCV RNA replication in cell culture. Science. 2000;290:1972–4. - PubMed
-
- Kim JL, Morgenstern KA, Lin C, et al. Crystal structure of the hepatitis C virus NS3 protease domain complexed with a synthetic NS4A cofactor peptide. Cell. 1996;87:343–55. - PubMed
-
- Yao N, Hesson T, Cable M, et al. Structure of the hepatitis C virus RNA helicase domain. Nat Struct Biol. 1997;4:463–7. - PubMed
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