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Published on: July 31, 2021
Maternal immunization promotes the immune response of neonates towards hepatitis B vaccine
1Department of Epidemiology, School of Public Health, The Fourth Military Medical University, Xi'an, China.
Insights
Maternal hepatitis B vaccination may boost infant immune response. High maternal anti-hepatitis B surface antigen (anti-HBs) levels correlate with improved infant hepatitis B virus (HBV) vaccine effectiveness, even with delayed infant vaccination.
Area of Science:
- Immunology
- Vaccinology
- Public Health
Background:
- Hepatitis B virus (HBV) infection poses severe risks to infants.
- Despite universal vaccination, some newborns fail to achieve protective anti-hepatitis B surface antigen (anti-HBs) titres.
Purpose of the Study:
- To investigate the impact of maternal hepatitis B vaccination on neonatal HBV vaccination outcomes.
- To determine factors influencing infant anti-HBs titres.
Main Methods:
- Animal experiments using vaccinated and unvaccinated sows and piglets.
- Population-based cross-sectional study of 449 mothers and their infants.
- Measurement of anti-HBs titres and analysis of demographic and medical data.
Main Results:
- Vaccinated piglets born to vaccinated sows showed significantly higher anti-HBs titres than those born to unvaccinated sows.
- Delayed first infant vaccination dose and higher maternal anti-HBs titres were key predictors of neonatal anti-HBs levels.
Conclusions:
- High maternal anti-HBs titres can positively influence infant response to HBV vaccination.
- Maternal vaccination status and antibody levels are important considerations for neonatal HBV immunization strategies.
Abstract:
Infants infected with hepatitis B virus (HBV) face the risk of developing severe complications. Unfortunately, in spite of universal vaccination programmes, 5% or more of vaccinated newborns still do not achieve protective levels of anti-hepatitis B virus surface antigen titres (anti-HBs). The aim of this study was to use animal experiments and population-based research to determine whether maternal vaccination against HBV affects the outcome of neonatal vaccination. Six sows and 53 newborn piglets were used for this study and randomly assigned to the vaccination group (three 20 μg doses of recombinant HBV vaccine). All the piglets were followed up to 10 weeks of age, and peripheral blood was withdrawn for measurement of anti-HBs. A cross-sectional study was also conducted on 449 mothers with infants. A structured questionnaire was used to collect demographic, medical and maternal data, and their peripheral blood was collected for measurement of anti-HBs. The results of animal experiments demonstrated that nonvaccinated piglets born to vaccinated sows and nonvaccinated piglets born to nonvaccinated sows were negative for anti-HBs. Repeated measures analysis of variance showed that the titres of anti-HBs in vaccinated piglets born to vaccinated sows were significantly higher than in vaccinated piglets born to nonvaccinated sows (P < 0.05). In a population-based study, a cumulative logistic regression analysis showed that the strongest influences on neonatal anti-HBs titres were delay of the first vaccination dose [OR = 3.02(95% CI: 1.72-5.30)] and maternal anti-HBs titres [OR = 2.48(95% CI: 2.03-3.04)]. In conclusion, high maternal anti-HBs titres can enhance the response to HBV vaccination in infants.
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