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Anti-HBs kinetics after HBV vaccination in neonates
R Vranckx1, A Alisjahbana, W Ngantung
1Institute of Hygiene and Epidemiology, Brussels, Belgium.
Insights
Hepatitis B vaccine kinetics in newborns are similar to adults, suggesting personalized booster schedules based on individual antibody titers can optimize long-term protection against HBV infection.
Area of Science:
- Immunology
- Vaccinology
- Pediatrics
Background:
- Hepatitis B virus (HBV) infection poses a significant risk in endemic areas.
- Recombinant DNA HBV vaccines are crucial for preventing perinatal transmission.
Purpose of the Study:
- To evaluate anti-HBs antibody kinetics in newborns vaccinated with a recombinant DNA HBV vaccine.
- To compare neonatal anti-HBs kinetics with adult data for booster vaccination needs.
- To estimate the optimal timing for booster vaccinations in neonates.
Main Methods:
- 148 neonates received a recombinant DNA HBV vaccine and were followed for 62 months.
- Neonates were categorized into 'exposed' and 'non-exposed' groups based on maternal HBV surface antigen status.
- Anti-HBs antibody titers were measured over time to assess vaccine effectiveness and decay.
Main Results:
- Neonatal anti-HBs titers were comparable to adult levels at 60 months post-vaccination.
- Individual titer calculations predicted that 8.3% of neonates require a booster within 14 months, 26.7% within 50 months, and 65% after 50 months.
- A minimum anti-HBs level of 10 IU/L was used as the threshold for protection.
Conclusions:
- Anti-HBs kinetics are similar in neonates and adults, supporting comparable vaccination strategies.
- Individual titer monitoring post-booster vaccination is an effective method for determining personalized booster intervals.
- This approach offers a cost-effective strategy for maintaining long-term protection against HBV in vaccinated neonates.
Background And Objectives:
We report the results of a study using a recombinant DNA HBV vaccine in newborns from an endemic area for HBV and compare the anti-HBs kinetics with observations in adults in order to make estimates about the need for booster vaccinations.
Study Design:
One hundred and forty-eight neonates were vaccinated and followed for 62 months. Based on the presence or absence of hepatitis B surface antigen in the mother, cohorts of 'exposed' and of 'non-exposed' neonates were identified.
Results:
A maximum concentration is normally observed after the booster vaccination followed by a rapid decline. According to Ambrosch et al. and Gesemann et al., titer calculations as a function of time, yielded 37 IU/1 and 47 IU/1 at month 60 respectively. The mean titer for the three groups of neonates investigated was at that time 74 IU/1. The prospective time intervals to arrive at an anti-HBs level of at least 10 IU/1 can be individually calculated from the individual titer after the booster vaccination. These calculated estimates show respectively: that 8.3% of the vaccinated neonates need a new booster vaccination within 14 months; that 26.7% will need a new booster within 50 months; and that only 65% need a new booster in 50 or more months.
Conclusion:
It can be concluded that anti-HBs kinetics in very young children and adults are comparable. The least expensive way of maintaining protection against HBV in neonates seems to be the determination of the individual titers after the first booster vaccination and calculation of the prospective time interval to arrive at a minimum titer of 10 IU/1 and the need for a new booster vaccination.
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