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Humoral immune responses to Neisseria meningitidis in children

A J Pollard1, R Galassini, E M van der Voort

  • 1Departments of Paediatrics and Infectious Diseases & Microbiology, Imperial College School of Medicine, St. Mary's Hospital, London W2 1PG, United Kingdom. AJPollard@csi.com

Insights

Infants show poor immune response to meningococcal B infections, despite producing similar antibody levels to older children. This suggests qualitative antibody differences, not class switching failures, impact infant immunity to Neisseria meningitidis.

Area of Science:

  • Immunology
  • Pediatrics
  • Microbiology

Background:

  • Understanding childhood immunity to serogroup B meningococci is crucial for developing effective infant vaccines.
  • Previous studies indicate suboptimal immune responses in infants, necessitating investigation into the underlying mechanisms.

Purpose of the Study:

  • To investigate the characteristics of humoral immune responses to Neisseria meningitidis infection in relation to age.
  • To identify factors contributing to poor vaccine responses in infancy.

Main Methods:

  • Analysis of serum bactericidal activity in children of different age groups following Neisseria meningitidis infection.
  • Measurement of total immunoglobulin G (IgG) and IgG subclass antibodies using enzyme-linked immunosorbent assay (ELISA).

Main Results:

  • Serum bactericidal activity against serogroup B meningococci was significantly lower in children under 12 months compared to older children.
  • Infants produced comparable levels of total IgG and specific IgG subclasses (IgG1 and IgG3) to older children.
  • Highest bactericidal activity was observed in children over 10 years of age.

Conclusions:

  • The age-dependent variation in bactericidal antibody response following meningococcal infection is not attributed to impaired immunoglobulin class switching in infants.
  • Qualitative differences in antibody specificity or affinity may explain the reduced bactericidal capacity in infants.

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