Serotype-specific and age-dependent generation of pneumococcal polysaccharide-specific memory B-cell and antibody

Elizabeth A Clutterbuck1, Sarah Oh, Mainga Hamaluba

  • 1Department of Paediatrics, Centre for Clinical Vaccinology and Tropical Medicine, University of Oxford, The Churchill Hospital,Oxford, Oxfordshire, United Kingdom. elizabeth.clutterbuck@paediatrics.ox.ac.uk

Insights

Two doses of pneumococcal conjugate vaccine (PCV) are needed in toddlers to achieve antibody and memory B-cell responses comparable to adults. This ensures sustained protection against encapsulated bacterial diseases.

Area of Science:

  • Immunology
  • Vaccinology
  • Pediatrics

Background:

  • Glycoconjugate vaccines reduce encapsulated bacterial diseases in young children.
  • Antibody levels from vaccines in toddlers under 2 years wane rapidly.

Purpose of the Study:

  • Compare B-cell and antibody responses to heptavalent pneumococcal conjugate vaccine (PCV) in adults and 12-month-old toddlers.
  • Determine the impact of a second PCV dose on immune responses in toddlers.

Main Methods:

  • Enzyme-linked immunospot assay used to measure diphtheria toxoid and specific polysaccharide-reactive plasma and memory B cells.
  • Immunization of adults and toddlers with PCV, with toddlers receiving a second dose at 14 months.

Main Results:

  • Toddlers lacked pre-existing polysaccharide-specific memory B cells and serum IgG but had diphtheria toxoid responses.
  • A single PCV dose increased plasma and memory B cells in both groups, but responses were lower in toddlers.
  • IgM dominated toddler antibody responses, with serotype-dependent class switching to IgG.
  • A second PCV dose enhanced antibody and memory B-cell responses in toddlers.

Conclusions:

  • Two doses of PCV are necessary for toddlers to generate memory B-cell frequencies and antibody class switching for pneumococcal polysaccharides comparable to adults.
  • This suggests a two-dose regimen is required for sustained protection in toddlers.

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