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Published on: April 5, 2019
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.
Abstract:
Glycoconjugate vaccines have dramatically reduced the incidence of encapsulated bacterial diseases in toddlers under 2 years of age, but vaccine-induced antibody levels in this age group wane rapidly. We immunized adults and 12-month-old toddlers with heptavalent pneumococcal conjugate vaccine to determine differences in B-cell and antibody responses. The adults and 12-month-old toddlers received a pneumococcal conjugate vaccine. The toddlers received a second dose at 14 months of age. The frequencies of diphtheria toxoid and serotype 4, 14, and 23F polysaccharide-specific plasma cells and memory B cells were determined by enzyme-linked immunospot assay. The toddlers had no preexisting polysaccharide-specific memory B cells or serum immunoglobulin G (IgG) antibody but had good diphtheria toxoid-specific memory responses. The frequencies of plasma cells and memory B cells increased by day 7 (P < 0.0001) in the adults and the toddlers following a single dose of conjugate, but the polysaccharide responses were significantly lower in the toddlers than in the adults (P = 0.009 to <0.001). IgM dominated the toddler antibody responses, and class switching to the IgG was serotype dependent. A second dose of vaccine enhanced the antibody and memory B-cell responses in the toddlers but not the ex vivo plasma cell responses. Two doses of pneumococcal conjugate vaccine are required in toddlers to generate memory B-cell frequencies and antibody class switching for each pneumococcal polysaccharide equivalent to that seen in adults.
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