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Published on: September 25, 2019
Long term effect of alpha interferon in children with chronic hepatitis B
F Bortolotti1, P Jara, C Barbera
1Clinica Medica 5, University of Padua, Italy.
Insights
Interferon alpha (IFN) treatment for chronic hepatitis B in children did not improve long-term HBeAg clearance rates compared to controls. However, IFN accelerated HBsAg loss in patients with active disease who responded early.
Area of Science:
- Pediatric Hepatology
- Viral Hepatitis Research
- Immunomodulatory Therapy
Background:
- Chronic hepatitis B (CHB) infection in children requires long-term management and prognosis assessment.
- Interferon (IFN) alpha has been used to treat CHB, but its long-term impact on disease progression in pediatric populations needs further definition.
Purpose of the Study:
- To define the long-term prognosis of chronic hepatitis B infection in children treated with interferon alpha.
- To evaluate the sustained efficacy of IFN alpha in pediatric CHB patients.
Main Methods:
- A cohort of 107 children with CHB received IFN alpha for 3-6 months and were followed for a mean of 69 months.
- Treatment response was defined by hepatitis B e antigen (HBeAg) loss within 12 months post-treatment.
- A control group of 59 untreated children was followed for a mean of 46 months.
Main Results:
- Sustained HBeAg clearance rates at five years were similar between IFN-treated children (60%) and controls (65%).
- High baseline transaminases and histological activity index predicted treatment response.
- Hepatitis B surface antigen (HBsAg) loss occurred in 25% of early responders treated with IFN, but not in non-responders or controls.
Conclusions:
- IFN alpha treatment in children with CHB appears to accelerate spontaneous HBeAg clearance rather than increase the overall rate.
- IFN alpha significantly enhanced HBsAg loss in children with active disease who responded early, suggesting a specific benefit for this subgroup.
Background/Aims:
The purpose of this study was to better define the long term prognosis of infection and disease in children with chronic hepatitis B treated with interferon (IFN) alpha.
Patients:
A total of 107 children with chronic hepatitis B who received IFN alpha for three or six months in two clinical trials were followed for a mean period of 69 (17) months. Response to treatment was defined as loss of hepatitis B e antigen (HBeAg) within 12 months after stopping treatment. A control group of 59 patients was also followed for a shorter mean time (46 (19) months).
Results:
Sixteen (15%) treated children responded during therapy and 18 (17%) during post-treatment follow up; 31 (29%) non-responders lost HBeAg during subsequent years. High pretreatment levels of transaminases and a greater histological activity index were predictors of response. Kaplan-Meier estimates of cumulative HBeAg clearance rates at five years were similar between treated patients (60%) and controls (65%). After HBeAg clearance, all cases lost hepatitis B virus DNA and 94% had normal transaminase levels. Loss of hepatitis B surface antigen (HBsAg) occurred in four (25%) patients who responded during treatment but in none of the other treated or untreated patients.
Conclusions:
After five years' observation, the proportion of treated children with sustained HBeAg clearance comprised an equal number of responders and non-responders and did not differ from that observed in untreated controls, suggesting that IFN simply accelerated a spontaneous event. However, IFN significantly improved the rate of HBsAg loss in cases with more prominent disease activity who were early responders, and may be particularly useful in this type of patient.
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