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Updated: May 2, 2026

Determination of Vaccine Immunogenicity Using Bovine Monocyte-Derived Dendritic Cells
Published on: May 19, 2023
Polysaccharide-specific B cell responses to vaccination in humans
Ruth Mitchell1, Dominic F Kelly1, Andrew J Pollard1
1Oxford Vaccine Group; Department of Paediatrics; University of Oxford and the NIHR Oxford Biomedical Research Centre; Oxford, UK.
Vaccines for bacterial meningitis and pneumonia reduce disease, but B cell responses, particularly in infants, are less understood. Booster doses significantly enhance these critical immune cell responses.
Area of Science:
- Immunology
- Vaccinology
- Microbiology
Background:
- Vaccines targeting capsular polysaccharides of *N. meningitidis*, *S. pneumoniae*, and *H. influenzae* type b have decreased disease incidence.
- While antibody responses are known, the underlying B cell populations (plasma cells and memory B cells) are less characterized.
Purpose of the Study:
- To summarize plasma cell (PC) and memory B cell (BMEM) responses after polysaccharide and conjugate vaccination.
- To compare these responses across different vaccine types and age groups.
Main Methods:
- Review and synthesis of existing studies on B cell responses to polysaccharide and conjugate vaccines.
- Analysis of data from various age groups, including infants and older individuals.
Main Results:
- Infant primary PC and BMEM responses to conjugate vaccines are lower than in older groups but increase substantially after booster doses.
- PC kinetics are similar across vaccine types and ages, while BMEM responses differ between plain polysaccharide and conjugate vaccines.
- A correlation between early BMEM responses and sustained antibody levels is suggested but not fully elucidated.
Conclusions:
- Booster doses are crucial for enhancing infant B cell responses to polysaccharide-conjugate vaccines.
- Understanding B cell subset induction mechanisms is key to improving vaccine-induced protective immunity.
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