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Lamivudine and high-dose interferon-alpha combination therapy for naive children with chronic hepatitis B infection
Inci Nur Saltik-Temizel1, Nurten Koçak, Hülya Demir
1Hacettepe University, Faculty of Medicine, Department of Pediatrics, Section of Gastroenterology, Hepatology and Nutrition, Ankara, Turkey. isaltik@hacettepe.edu.tr
Insights
This study explored lamivudine and interferon-alpha combination therapy for children with chronic hepatitis B. The treatment showed promising results, with over half achieving virologic response and clearing hepatitis B e antigen.
Area of Science:
- Pediatric Hepatology
- Virology
- Immunotherapy
Background:
- Chronic hepatitis B affects many children, with over 50% not responding to interferon-alpha therapy alone.
- Identifying effective treatment strategies for pediatric chronic hepatitis B is crucial.
Purpose of the Study:
- To evaluate the efficacy of a combination therapy involving lamivudine and interferon-alpha in children with chronic hepatitis B.
- To assess this regimen following an initial 3-month lamivudine induction phase.
Main Methods:
- Twenty treatment-naive children received 3 months of lamivudine monotherapy.
- Interferon-alpha was added for 6 months, followed by continued lamivudine for another 6 months.
- Virologic response was defined by HBV DNA negativity and HBeAg loss with AntiHBe seroconversion.
Main Results:
- Virologic response was achieved in 55% (11/20) of patients after 15 months.
- Hepatitis B e antigen (HBeAg) clearance occurred in 60% (12/20) of patients.
- The combination therapy was well-tolerated by the pediatric participants.
Conclusions:
- Lamivudine and high-dose interferon-alpha combination therapy, following lamivudine induction, appears to be an effective treatment option.
- This regimen shows potential for improving outcomes in children with chronic hepatitis B.
- Further research may validate this approach for pediatric hepatitis B management.
Background:
More than half of the children with chronic hepatitis B infection are nonresponders to interferon-alpha. The aim of this study was to investigate the efficacy of lamivudine and interferon-alpha combination therapy after a 3-month lamivudine induction in children with chronic hepatitis B.
Study:
Twenty naive children were given lamivudine (4 mg/kg per day; maximum, 100 mg) alone for 3 months; then interferon-alpha (10 MU/m, thrice weekly) was added to lamivudine for 6 months. After interferon-alpha was stopped, lamivudine alone was continued for 6 months. Therapy was stopped 6 months after HBeAg seroconversion. Every 3 months, HBV markers were studied and virologic response was defined as HBV DNA negativity, and HBeAg loss with AntiHBe seroconversion.
Results:
At the end of 15 months, virologic response was achieved in 11 (55%) of patients and 12 patients (60%) cleared hepatitis B e antigen. Therapy was well tolerated.
Conclusion:
Preliminary results of our study seem to indicate that lamivudine and high-dose interferon-alpha combination therapy after a 3-month lamivudine induction may represent an effective treatment option for children with chronic hepatitis B.
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