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Published on: September 25, 2019
Functional cure is associated with younger age in children undergoing antiviral treatment for active chronic
Min Zhang1, Jing Li2, Zhiqiang Xu1
1Department of Liver Diseases, National Clinical Research Center for Infectious Diseases, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Insights
Younger children (1-7 years) with chronic hepatitis B (CHB) achieved higher functional cure rates with antiviral therapy compared to older children (≥7 years). Early treatment in pediatric CHB patients is supported by these findings.
Area of Science:
- Hepatology
- Virology
- Pediatric Infectious Diseases
Background:
- Functional cure for chronic hepatitis B (CHB) remains challenging with current antiviral therapies.
- Limited data exist on treatment outcomes in pediatric populations with CHB.
Purpose of the Study:
- To assess the frequency of functional cure in children with active CHB undergoing antiviral treatment.
- To compare treatment outcomes between different age groups of pediatric CHB patients.
Main Methods:
- Retrospective study of 372 children (aged 1-16 years) with active CHB.
- Treatment included nucleos(t)ide analog monotherapy or combination therapy with interferon-α (IFN-α) for 24-36 months.
- Functional cure defined by hepatitis B virus (HBV) DNA loss, HBeAg loss/seroconversion, and HBsAg loss.
Main Results:
- Children aged 1-7 years showed significantly higher rates of HBV DNA clearance, HBeAg seroconversion, and HBsAg loss compared to those aged ≥7-16 years.
- Younger children (1-7 years) experienced more rapid reductions in HBV DNA, HBeAg, and HBsAg levels.
- Lower baseline HBsAg levels (<1,500 IU/mL) were associated with improved cure rates; no serious adverse events were reported.
Conclusions:
- Children aged 1-7 years with active CHB achieve higher functional cure rates with antiviral therapy than older children.
- These findings support early antiviral treatment initiation for pediatric CHB.
- Further prospective randomized controlled trials are needed to validate these results.
Background And Aims:
Functional cure is difficult to achieve using current antiviral therapies; moreover, limited data are available regarding treatment outcomes in children. This retrospective study aimed to assess the frequency of functional cure among children undergoing antiviral treatment for active chronic hepatitis B (CHB).
Methods:
A total of 372 children aged 1-16 years, with active CHB were enrolled and underwent either nucleos(t)ide analog monotherapy or combination therapy with interferon-α (IFN-α) for 24-36 months. All children attended follow-up visits every 3 months. Functional cure was defined as evidence of hepatitis B virus (HBV) DNA loss, circulating hepatitis B e antigen (HBeAg) loss/seroconversion, and hepatitis B surface antigen (HBsAg) loss.
Results:
After 36 months of antiviral treatment and/or follow-up visits, children with CHB aged 1- < 7 years exhibited higher rates of HBV DNA clearance, HBeAg seroconversion, and HBsAg loss than CHB children ≥ 7-16 years of age (93.75% versus [vs.] 86.21% [p < 0.0001]; 79.30% vs. 51.72% [p < 0.0001]; and 50.78% vs. 12.93% [p < 0.0001], respectively). Longitudinal investigation revealed more rapid dynamic reduction in HBV DNA, HBeAg, and HBsAg levels in children aged 1-7 years than in those aged ≥ 7-16 years with CHB. According to further age-stratified analysis, HBsAg loss rates were successively decreased in children with CHB who were 1- < 3, 3- < 7, 7- < 12, and 12-16 years of age (62.61% vs. 41.13% vs. 25.45% vs. 1.64%, respectively; p < 0.0001) at 36 months. In addition, baseline HBsAg level < 1,500 IU/mL was found to favor disease cure among these pediatric patients. No serious adverse events were observed throughout the study period.
Conclusion:
Results of the present study demonstrated that children aged 1- < 7 years, with active CHB can achieve a high functional cure rate by undergoing antiviral therapy compared to those aged ≥ 7 years, who undergo antiviral therapy. These data support the use of antiviral treatment at an early age in children with CHB. However, future prospectively randomized controlled trials are necessary to validate the findings of this study.
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