| Literature DB >> 29280054 |
Abstract
Chronic hepatitis B infection is caused by hepatitis B virus (HBV) and a total cure is yet to be achieved. The viral covalently closed circular DNA (cccDNA) is the key to establish a persistent infection within hepatocytes. Current antiviral strategies have no effect on the pre-existing cccDNA reservoir. Therefore, the study of the molecular mechanism of cccDNA formation is becoming a major focus of HBV research. This review summarizes the current advances in cccDNA molecular biology and the latest studies on the elimination or inactivation of cccDNA, including three major areas: (1) epigenetic regulation of cccDNA by HBV X protein, (2) immune-mediated degradation, and (3) genome-editing nucleases. All these aspects provide clues on how to finally attain a cure for chronic hepatitis B infection.Entities:
Keywords: HBx; covalently closed circular DNA (cccDNA); genome-editing nucleases; hepatitis B virus (HBV); immunemediated
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Year: 2017 PMID: 29280054 PMCID: PMC6598884 DOI: 10.1007/s12250-017-4009-4
Source DB: PubMed Journal: Virol Sin ISSN: 1995-820X Impact factor: 4.327