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Immunogenicity and immunologic memory of meningococcal C conjugate vaccine in premature infants
Clare L Collins1, Jens U Ruggeberg, Gail Balfour
1St. George's Hospital Medical School, London, United Kingdom.
Insights
Meningococcal C conjugate (MCC) vaccine primes immune memory in preterm infants, but antibody levels wane. Preterm infants showed lower responses to a booster, suggesting a need for routine booster doses, especially for preterm infants.
Area of Science:
- Immunology
- Vaccinology
- Pediatrics
Background:
- Meningococcal C conjugate (MCC) vaccines are crucial for preventing Neisseria meningitidis serogroup C infections.
- Routine immunization schedules in the UK included MCC vaccines starting in 1999.
- This study investigates antibody persistence and immune memory induction by MCC vaccine in preterm infants.
Purpose of the Study:
- To assess the immunogenicity and immune memory induction of the MCC vaccine in preterm infants.
- To compare immune responses in preterm infants to those of term infants.
- To evaluate the impact of prematurity on vaccine effectiveness.
Main Methods:
- A cohort of 62 preterm and 60 term infants received MCC vaccine on an accelerated schedule (2, 3, and 4 months).
- Immunogenicity and immune memory were assessed after primary immunization.
- A meningococcal C polysaccharide challenge was administered at 12 months of age to evaluate immune memory.
Main Results:
- Both preterm and term infants achieved similar protective antibody titers after primary immunization.
- Antibody titers significantly waned by 1 year of age in both groups.
- Post-challenge serum bactericidal activity was significantly lower in preterm infants (P = 0.03), with 73% achieving a 4-fold rise versus 88% in term controls (P = 0.07).
Conclusions:
- The MCC vaccine is immunogenic and primes for immune memory in preterm infants.
- Preterm infants exhibit decreased memory responses compared to term infants.
- Findings suggest a role for a routine booster dose of MCC vaccine in all infants, particularly those born preterm, due to waning immunity.
Background:
Protein-polysaccharide conjugate vaccines against Neisseria meningitidis serogroup C were introduced into the U.K. routine immunization schedule in 1999. This study is the first to describe both persistence of antibody and evidence for induction of immune memory using meningococcal C conjugate (MCC) vaccine in preterm infants.
Methods:
Immunogenicity and induction of immunologic memory by as MCC vaccine was assessed in premature infants; 62 preterm and 60 term controls received MCC at the accelerated schedule (2, 3 and 4 months of age). A meningococcal C polysaccharide challenge was administered at 12 months of age.
Results:
Both groups achieved similar protective titers after primary immunization that then waned significantly by 1 year of age. Postchallenge serum bactericidal activity was significantly lower in preterm infants (P = 0.03); 73% of preterm versus 88% of term controls achieved a 4-fold rise in serum bactericidal activity (P = 0.07).
Conclusions:
MCC vaccine is immunogenic and primes for immunologic memory in preterm infants. The decreased memory responses in these preterm infants in conjunction with waning clinical efficacy data for all U.K. infants suggest a role for a routine booster dose of vaccine in all infants receiving MCC, especially those born preterm.
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