Hepatology International2011Full TextOpen AccessHighly Cited

HBV life cycle and novel drug targets

Daniela Grimm, Robert Thimme, Hubert E. Blum

113 citations2011Open Access — see publisher for license terms1 related compound

Research Article — Peer-Reviewed Source

Original research published by Grimm et al. in Hepatology International. Redistributed under Open Access — see publisher for license terms. MedTech Research Group provides these references for informational purposes. We do not conduct original research. All studies are the work of their respective authors and institutions.

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Abstract

With up to 400 million affected people worldwide, chronic hepatitis B virus (HBV) infection is still a major health care problem. During the last decade, several novel therapeutic approaches have been developed and evaluated. In most regions of the world, interferon-α, and nucleos(t)ide analogues (NUCs) are currently approved. Despite major improvements, none of the existing therapies is optimal since viral clearance is rarely achieved. Recently, a better understanding of the HBV life cycle and the development of novel model systems of HBV infection have led to the development of novel antiviral strategies and drug targets. This review will focus on current and potential future drug targets in the HBV life cycle and strategies to modulate the virus–host interaction.

Article Details
DOI10.1007/s12072-011-9261-3
PubMed ID21484123
PMC IDPMC3090558
JournalHepatology International
Year2011
AuthorsDaniela Grimm, Robert Thimme, Hubert E. Blum
LicenseOpen Access — see publisher for license terms
Citations113