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Modeling Hepatitis B Virus Infection in Non-Hepatic 293T-NE-3NRs Cells
Published on: June 5, 2020
Hepatitis B virus infection in children
C S O'Gorman1, K O'Connell, A M Broderick
1Our Lady's Children's Hospital, Crumlin, Dublin.
Insights
Universal neonatal vaccination for Hepatitis B virus (UNV-HBV) could prevent 22% of pediatric cases and limit spread. This supports the recent introduction of UNV-HBV in Ireland.
Area of Science:
- Pediatric Infectious Diseases
- Hepatology
- Public Health
Background:
- Recent increases in Hepatitis B virus (HBV) infection necessitate understanding the pediatric landscape.
- Characterizing HBV-infected children in Ireland is crucial for effective management and prevention strategies.
Purpose of the Study:
- To characterize HBV-infected children in Ireland.
- To audit the management of pediatric HBV cases.
- To evaluate the potential impact of universal neonatal vaccination (UNV-HBV).
Main Methods:
- Prospective data review of 46 HBV-infected children in Ireland.
- Analysis of demographic, acquisition, HBV-DNA levels, and Hepatitis B e antigen (HBeAg) status.
- Estimation of UNV-HBV impact on case prevention and horizontal spread.
Main Results:
- The study included 46 children, with a median age of 8.1 years; 50% were European.
- Vertical transmission accounted for 54.3% of cases; 62.5% had high HBV-DNA levels.
- HBeAg was detected in 72.7% of cases.
Conclusions:
- Universal neonatal vaccination (UNV-HBV) could have prevented an estimated 22% of identified pediatric HBV cases.
- UNV-HBV is a key strategy to limit further horizontal HBV transmission.
- The findings strongly support the recent implementation of UNV-HBV.
Abstract:
Recent increases in Hepatitis B virus (HBV) infection prompted us to characterize HBV-infected children in Ireland and to audit management, by reviewing prospectively gathered data. Of 46 children (29 [63%] male), median age at presentation was 8.1 years (range 0.6-17.6), monitoring duration was 22.5 months (range 1-101), 23/46 (50%) were European (including 9 [19.6%] Irish), 15 (32.6%) African and 9 (19.6%) Asian. Acquisition was vertical (25/46 [54.3%]), horizontal (5/46 [10.9%]), unknown (16/46 [34.8%]). HBV-DNA was >100,000,000 cpm in 20/32 (62.5%) with chronic infection. Hepatitis B e antigen (HBeAg) was detected in 32/44 (72.7%). We estimate that universal neonatal vaccination (UNV-HBV) could have prevented 22% of cases, and could limit further horizontal HBV spread. This supports the recent introduction of UNV-HBV.
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