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Updated: Feb 5, 2026

Surface Functionalization of Hepatitis E Virus Nanoparticles Using Chemical Conjugation Methods
Published on: May 11, 2018
[The multiple functions of the hepatitis B virus core protein: new research directions and therapeutic challenges]
Hélène Chabrolles1, Thomas Lahlali1, Héloïse Auclair1
1Centre de recherche en cancérologie de Lyon (CRCL), Inserm U1052, 151, cours Albert Thomas, 69003 Lyon, France.
Insights
Chronic hepatitis B virus (HBV) infection affects millions globally, risking liver disease. New treatments targeting the HBV Core protein are needed to improve viral control, as current therapies don't eradicate the virus.
Area of Science:
- Hepatology
- Virology
- Drug Discovery
Background:
- Chronic hepatitis B virus (HBV) infection is a significant global health issue, leading to severe liver conditions like cirrhosis and hepatocellular carcinoma.
- Current antiviral treatments can lower HBV levels but fail to eliminate the virus from liver cells, highlighting the need for novel therapeutic strategies.
Purpose of the Study:
- To explore new therapeutic targets for chronic HBV infection.
- To investigate the potential of targeting the HBV Core protein and its regulatory functions for antiviral drug development.
Main Methods:
- Focus on the HBV Core protein as a novel target for antiviral therapies.
- Exploration of Core protein Allosteric Modulators (CAMs) and host-targeting agents (HTAs).
Main Results:
- CAMs targeting HBV Core protein assembly are advancing in clinical trials.
- Investigating Core protein's regulatory roles may identify new cellular targets for combination therapies.
Conclusions:
- The HBV Core protein presents a promising target for developing new antiviral agents.
- Targeting viral assembly and host factors offers a potential strategy for improved HBV replication control.
Abstract:
Chronic infection by hepatitis B virus (HBV) is a major public health problem with more than 250 millions of people chronically infected worldwide who have a high risk to develop cirrhosis and hepatocellular carcinoma. Available treatments reduce viremia but do not eradicate the virus from hepatocytes. Therefore, there is an urgent need to develop new classes of antiviral molecules and the viral capsid protein, Core, constitutes a new favored target. Core protein Allosteric Modulators (CAMs) targeting its assembly functions are in clinical development. In addition, investigation of Core regulatory functions may lead to the development of compounds targeting cellular factors (HTA) that could be used in combined therapies aiming to achieve a better control of HBV replication.
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