Objective: To investigate whether combining the antiviral effect of lamivudine with the immune-boosting action of interferon-alpha (IFN-α) is effective in treating hepatitis B virus (HBV) "immunotolerant" children. Study design: Twenty-three children (8 boys; mean age, 10 years) infected during the first year of life (17 Asian, 21 with normal aminotransferase levels, 15 with HBV-DNA >1000 pg/mL by hybridization and all with mild histologic changes) were treated with lamivudine (3 mg/kg) for 8 weeks alone and then lamivudine (3 mg/kg) and IFN-α (5 MU/m2, 3 times weekly) in combination for 10 months. Results: Seventy-eight percent became HBV-DNA negative at the end of treatment, 5 (22%) seroconverted to anti-HBe, 4 (17%) of whom achieved complete viral control, becoming persistently HBsAg negative and anti-HBs positive. None had YMDD mutations. The viral status of the patients has not changed after a median follow-up of 40 months (range, 36 to 48). Conclusions: This pilot study suggests that lamivudine pretreatment followed by a combination of lamivudine and IFN-α can induce complete viral control in HBV immunotolerant children, hitherto considered poor responders.
D'Antiga, L., Aw, M., Atkins, M., Moorat, A., Vergani, D., Mieli-Vergani, G. (2006). Combined lamivudine/interferon-α treatment in 'immunotolerant' children perinatally infected with hepatitis B: A pilot study. THE JOURNAL OF PEDIATRICS, 148(2), 228-233 [10.1016/j.jpeds.2005.09.020].
Combined lamivudine/interferon-α treatment in 'immunotolerant' children perinatally infected with hepatitis B: A pilot study
D'Antiga, L;
2006
Abstract
Objective: To investigate whether combining the antiviral effect of lamivudine with the immune-boosting action of interferon-alpha (IFN-α) is effective in treating hepatitis B virus (HBV) "immunotolerant" children. Study design: Twenty-three children (8 boys; mean age, 10 years) infected during the first year of life (17 Asian, 21 with normal aminotransferase levels, 15 with HBV-DNA >1000 pg/mL by hybridization and all with mild histologic changes) were treated with lamivudine (3 mg/kg) for 8 weeks alone and then lamivudine (3 mg/kg) and IFN-α (5 MU/m2, 3 times weekly) in combination for 10 months. Results: Seventy-eight percent became HBV-DNA negative at the end of treatment, 5 (22%) seroconverted to anti-HBe, 4 (17%) of whom achieved complete viral control, becoming persistently HBsAg negative and anti-HBs positive. None had YMDD mutations. The viral status of the patients has not changed after a median follow-up of 40 months (range, 36 to 48). Conclusions: This pilot study suggests that lamivudine pretreatment followed by a combination of lamivudine and IFN-α can induce complete viral control in HBV immunotolerant children, hitherto considered poor responders.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.