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Booster vaccination after neonatal priming with acellular pertussis vaccine
Markus Knuf1, Heinz-Josef Schmitt, Jeanne-Marie Jacquet
1Department of Pediatrics, Johannes Gutenberg-University, Mainz, Germany. knuf@kinder.klinik.uni-mainz.de
Insights
Neonatal acellular pertussis (aP) vaccination primes infants for strong booster responses. However, this early priming may interfere with the immune response to hepatitis B virus (HBV), Haemophilus influenza type b (Hib), and diphtheria antigens.
Area of Science:
- Immunology
- Vaccinology
- Pediatric Infectious Diseases
Background:
- Infant vaccination schedules often include combined vaccines for multiple diseases.
- The impact of early pertussis vaccination on subsequent immune responses to other vaccine components is not fully understood.
Purpose of the Study:
- To evaluate the immunogenicity of a booster dose of DTaP-HBV-IPV/Hib vaccine in infants primed with a birth dose of acellular pertussis (aP).
- To assess whether neonatal aP priming induces immune tolerance or bystander interference with other vaccine antigens.
Main Methods:
- Infants received a birth dose of aP and a combined DTaP-HBV-IPV/Hib vaccine at 2, 4, and 6 months.
- A booster dose of DTaP-HBV-IPV/Hib was administered between 12 and 23 months.
- Antibody responses to pertussis, hepatitis B virus (HBV), Haemophilus influenza type b (Hib), and diphtheria antigens were measured.
Main Results:
- A booster dose of DTaP-HBV-IPV/Hib elicited strong anti-pertussis booster responses in infants.
- Neonatal aP priming did not result in immune tolerance to pertussis antigens.
- Neonatal aP priming was associated with bystander interference, potentially affecting immune responses to HBV, Hib, and diphtheria.
Conclusions:
- Early aP vaccination can effectively prime for pertussis booster responses.
- Neonatal aP priming may negatively impact the immune response to other antigens in combined vaccines.
- Further research is needed to optimize infant vaccination strategies to avoid potential interference.
Abstract:
After a birth dose of acellular pertussis (aP) and diphtheria (DT)aP-hepatitis B virus (HBV)-inactivated polio vaccine (IPV)/Haemophilus influenza type b (Hib) at 2, 4, and 6 months, a booster dose of DTaP-HBV-IPV/Hib at 12 to 23 months induced strong anti-pertussis booster responses. Thus, neonatal aP priming did not lead to immune tolerance to pertussis antigens. However, it elicited bystander interference on HBV, Hib, and diphtheria responses.
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