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Modeling Hepatitis B Virus Infection in Non-Hepatic 293T-NE-3NRs Cells
Published on: June 5, 2020
Epigenetic modulation in chronic hepatitis B virus infection
Maura Dandri1,2
1I. Department of Internal Medicine, Center for Internal Medicine, University Medical Center Hamburg-Eppendorf, Martinistr. 52, 20246, Hamburg, Germany. m.dandri@uke.de.
Insights
Chronic hepatitis B (CHB) persists due to immune evasion and viral DNA. Epigenetic modifications on viral and host DNA are key to understanding and potentially curing this persistent infection.
Area of Science:
- Virology
- Hepatology
- Epigenetics
Background:
- Hepatitis B virus (HBV) infection remains a global health challenge despite vaccines and antivirals.
- Persistent infection is enabled by immune system failure and the stable HBV covalently closed circular DNA (cccDNA) minichromosome.
- Understanding host-pathogen interactions, particularly epigenetic modifications, is crucial for HBV pathogenesis and cancer development.
Purpose of the Study:
- To review current knowledge on epigenetic mechanisms regulating HBV.
- To explore how epigenetic changes affect cccDNA activity and host cells.
- To highlight the role of epigenetics in HBV pathogenesis and potential therapeutic strategies.
Main Methods:
- Literature review of HBV epigenetic research.
- Analysis of studies on epigenetic modifications of cccDNA.
- Examination of host genome modifications in HBV-infected cells and tissues.
Main Results:
- Epigenetic modifications on cccDNA and host DNA are essential for modulating HBV activity.
- These epigenetic changes likely contribute to disease progression and liver cancer development.
- Limited but growing evidence points to epigenetics as a critical factor in HBV persistence.
Conclusions:
- Epigenetic regulation plays a significant role in the lifecycle and persistence of HBV.
- Targeting epigenetic mechanisms offers potential new strategies for controlling and curing chronic HBV infection.
- Further research into HBV epigenetics is vital for developing novel therapeutic interventions.
Abstract:
The human hepatitis B virus (HBV) is a small-enveloped DNA virus causing acute and chronic hepatitis. Despite the existence of an effective prophylactic vaccine and the strong capacity of approved antiviral drugs to suppress viral replication, chronic HBV infection (CHB) continues to be a major health burden worldwide. Both the inability of the immune system to resolve CHB and the unique replication strategy employed by HBV, which forms a stable viral covalently closed circular DNA (cccDNA) minichromosome in the hepatocyte nucleus, enable infection persistence. Knowledge of the complex network of interactions that HBV engages with its host is still limited but accumulating evidence indicates that epigenetic modifications occurring both on the cccDNA and on the host genome in the course of infection are essential to modulate viral activity and likely contribute to pathogenesis and cancer development. Thus, a deeper understanding of epigenetic regulatory processes may open new venues to control and eventually cure CHB. This review summarizes major findings in HBV epigenetic research, focusing on the epigenetic mechanisms regulating cccDNA activity and the modifications determined in infected host cells and tumor liver tissues.
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