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Detection of Low Copy Number Integrated Viral DNA Formed by In Vitro Hepatitis B Infection
Published on: November 7, 2018
Dual chronic hepatitis B virus and hepatitis C virus infection
Chun-Jen Liu1, Pei-Jer Chen, Ding-Shinn Chen
1Department of Internal Medicine, Graduate Institute of Clinical Medicine, Hepatitis Research Center, National Taiwan University College of Medicine and National Taiwan University Hospital, 1 Chang-Te Street, Taipei, 10002, Taiwan, cjliu@ntu.edu.tw.
Insights
Dual infections with hepatitis B (HBV) and C (HCV) viruses present complex challenges. Further research is needed to understand viral interactions, occult HBV, and optimal treatment strategies for co-infected patients.
Area of Science:
- Hepatology
- Virology
- Immunology
Background:
- Dual hepatitis B virus (HBV) and hepatitis C virus (HCV) infections are prevalent globally.
- Significant unresolved clinical and pathogenetic issues exist regarding these co-infections.
Purpose of the Study:
- To investigate the dynamics of HBV-HCV interactions within hepatocytes.
- To determine the prevalence and clinical impact of occult HBV in chronic HCV patients.
- To explore optimal treatment strategies and management of HBV reactivation in co-infected individuals.
Main Methods:
- Review of clinical and in vitro studies on viral interactions.
- Analysis of treatment outcomes for dual HBV/HCV infections.
- Investigation of HBV reactivation and HBsAg loss mechanisms.
Main Results:
- Combination therapy (peginterferon alfa-2a and ribavirin) shows similar efficacy and safety in dually infected patients compared to HCV monoinfection.
- One-third of dually infected patients with undetectable HBV DNA pre-treatment experienced HBV reactivation post-treatment.
- Approximately 10% of dually infected patients lost hepatitis B surface antigen (HBsAg).
Conclusions:
- Understanding HBV-HCV interactions within hepatocytes is crucial for future immunopathogenetic studies.
- Further research is required to establish optimal treatment strategies and prevent HBV reactivation in co-infected patients.
- Mechanisms underlying HBsAg loss in dually infected individuals need elucidation.
Abstract:
Dual hepatitis B virus (HBV) and hepatitis C virus (HCV) infection are common in HBV or HCV endemic areas. However, several clinical and pathogenetic issues remain unresolved. First, clinical and in vitro studies suggest the interactions between two viruses. The dynamics of the interaction in untreated setting versus treated setting and its influence on the long-term outcomes await further studies. A key issue regarding viral interactions is whether modulation of infection occurs in the same dually infected individual hepatocyte of the liver. Clarifying this issue may help to understand the reciprocal interference between HCV and HBV and provide clues for future immunopathogenetic studies. Second, the prevalence and clinical significance of coexisting occult HBV infection in patients with chronic HCV infection need further investigations. Third, combination therapy of peginterferon alfa-2a and ribavirin appears to be just as effective and safe for the treatment of hepatitis B surface antigen (HBsAg)-positive patients chronically infected with active chronic hepatitis C as it is in patients with HCV monoinfection. Nevertheless, one-third of dually infected patients with nondetectable serum HBV DNA-level pretreatment developed HBV reactivation posttreatment. How to prevent and treat this reactivation should be clarified. Furthermore, about 10% of the dually infected patients lost HBsAg. Underlying mechanisms await further investigations. Finally, the optimal treatment strategies for dually infected patients with hepatitis B e antigen-positive chronic hepatitis B should be identified in future clinical trials.
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