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Resolved HBV behavior during the treatment of chronic HCV infection with direct-acting antivirals
Salem Y Mohamed1, Baasim A Gaballah2, Hany Mohamed Elsadek1
1Gastroenterology and Hepatology Unit, Internal Medicine Department, Faculty of Medicine, Zagazig University, Zagazig, Egypt.
Insights
Treatment with direct-acting antiviral drugs (DAAs) for hepatitis C virus (HCV) showed a low risk of resolved hepatitis B virus (HBV) reactivation. This study followed patients with chronic hepatitis C, some with resolved HBV, during and after DAA therapy.
Area of Science:
- Hepatology
- Virology
- Internal Medicine
Background:
- Hepatitis B virus (HBV) and hepatitis C virus (HCV) co-infection is increasingly recognized.
- Previous studies on interferon therapy suggested a correlation between resolved HBV and lower treatment response, worse liver histology, and hepatocellular carcinoma development.
Purpose of the Study:
- To assess and follow the course of resolved HBV during and after direct-acting antiviral drugs (DAAs) treatment.
- To evaluate the risk of HBV reactivation in patients with chronic hepatitis C treated with DAAs.
Main Methods:
- An observational, prospective study included 313 patients with chronic hepatitis C (CHC), 60 of whom had resolved HBV infection.
- Patients received DAAs therapy for CHC and were monitored for viral markers (HCV RNA, HBV DNA) and liver enzymes (ALT, AST).
- Follow-up occurred at baseline, week 4, end of treatment, and 12 weeks post-treatment.
Main Results:
- Significant decreases in ALT and AST levels were observed in both groups, with stabilization during follow-up.
- Treatment efficacy was comparable between patients with and without resolved HBV.
- No cases of ALT flare were observed, indicating a low risk of HBV reactivation.
Conclusions:
- The risk of resolved HBV reactivation during or after DAAs treatment for CHC is low.
- DAAs therapy for CHC is safe in patients with resolved HBV infection.
Aim:
This paper aimed to assess and follow up the course of resolved HBV (hepatitis B virus) during and after treatment with direct-acting antiviral drugs (DAAs).
Background:
Co-infection with hepatitis B and hepatitis C is increasingly recognized in patients with chronic hepatitis. Resolved HBV in patients with chronic HCV (hepatitis C virus) infection has been investigated during interferon therapy, and the investigators suggest a possible correlation with a lower response to anti-viral treatment, higher grades of liver histological changes, and development of hepatocellular carcinoma.
Methods:
Three hundred and thirteen patients were included in our observational and prospective study; two hundred and fifty-three patients had chronic hepatitis C (CHC) (group I), and sixty patients had both CHC and resolved HBV-infection (group II). They all were eligible for treatment with DAAs therapy for chronic HCV in our hepatology unit, Internal Medicine Department, Zagazig University Hospitals from December 2017 to September 2018. They were subjected to thorough history taking, full clinical examination, routine laboratory investigations, HCV antibody, HCV RNA, HBV surface antigen (HBsAg), HBV surface antibody (anti-HBs) HBV core antibody (anti-HBc), and HBV-DNA quantitative levels. All patients were followed up at baseline, at the end of week 4 of anti-viral therapy, at the end of treatment and 12 weeks after treatment.
Results:
Assessment at 28 days showed significant decreases in ALT and AST levels in both groups, with stabilization of these levels on follow-up at 12 and 24 weeks. The efficacy of treatment was comparable in both groups. No case of ALT flare was observed in either group. Similar outcomes regarding AST and ALT levels were found in patients with diseases associated with immune derangement.
Conclusion:
The risk of resolved HBV reactivation during or after treatment with DAAs is low.
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