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Published on: December 19, 2020
Long-term protection after immunization with protein-polysaccharide conjugate vaccines in infancy
Geraldine Blanchard-Rohner1, Andrew J Pollard
1Oxford Vaccine Group, Department of Paediatrics, University of Oxford, UK. geraldine.blanchardrohner@paediatrics.ox.ac.uk
Insights
Protein-polysaccharide conjugate vaccines protect children from invasive bacterial infections like meningitis. Long-term immunity may require strategies to sustain antibody levels post-infant immunization.
Area of Science:
- Immunology
- Pediatrics
- Vaccinology
Background:
- Polysaccharide-encapsulated bacteria (Haemophilus influenzae type b, Neisseria meningitidis, Streptococcus pneumoniae) cause severe childhood infections globally.
- Protein-polysaccharide conjugate vaccines have significantly reduced invasive bacterial diseases in children.
- Herd immunity is vital, but sustained individual protection relies on antibodies and immunological memory.
Purpose of the Study:
- To detail protective mechanisms against encapsulated bacteria.
- To describe age-dependent immune responses to conjugate vaccines.
- To propose strategies for sustained protection against bacterial infections.
Main Methods:
- Review of existing literature on bacterial pathogenesis and vaccine immunology.
- Analysis of B-cell and antibody responses to protein-polysaccharide conjugate vaccines.
- Exploration of immunological memory persistence and antibody decay post-vaccination.
Main Results:
- Encapsulated bacteria pose a significant global health threat in pediatric populations.
- Conjugate vaccines are effective but may not ensure lifelong individual immunity.
- Antibody levels and vaccine effectiveness can wane post-infant immunization despite memory cell presence.
Conclusions:
- Understanding immune responses to conjugate vaccines is crucial for optimizing pediatric immunization strategies.
- Strategies are needed to ensure durable protection against encapsulated bacterial pathogens.
- Further research should focus on enhancing and sustaining vaccine-induced immunity throughout childhood.
Abstract:
The polysaccharide-encapsulated bacteria, Haemophilus influenzae type b, Neisseria meningitidis and Streptococcus pneumoniae are important causes of invasive bacterial infection in childhood, accounting for most of the cases of bacterial pneumonia and meningitis worldwide. Protein-polysaccharide conjugate vaccines have been developed over the last 20 years and have proven very effective in controlling these infections. Although studies have consistently shown that herd immunity is critical for population protection, long-term individual protection against polysaccharide-encapsulated bacteria appears to depend on persisting antibody and, perhaps to a lesser extent, immunological memory. However, some studies have reported that the concentration of serum antibody and vaccine effectiveness are not sustained after infant immunization, despite persistence of immunological memory. In this article, we detail the mechanisms of protection against invasion by encapsulated bacteria, describe the age-dependent B-cell and antibody responses to protein-polysaccharide conjugate vaccines and propose strategies to guarantee protection during periods of increased disease burden.
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