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Updated: May 23, 2026

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Published on: February 15, 2013
Use of pneumococcal polysaccharide vaccine in children: what is the evidence?
Ray Borrow1, Paul T Heath, Claire-Anne Siegrist
1Vaccine Evaluation Unit, Health Protection Agency, Clinical Sciences Building 2, Manchester Royal Infirmary, Manchester, UK. ray.borrow@hpa.org.uk
Insights
Pneumococcal polysaccharide vaccine (PPV23) may offer some protection against invasive pneumococcal disease (IPD) but carries a theoretical risk of B-cell depletion in children vaccinated with pneumococcal conjugate vaccines (PCVs). Optimal use in at-risk children remains unclear.
Area of Science:
- Immunology
- Vaccinology
- Pediatrics
Background:
- Pneumococcal conjugate vaccines (PCVs) are standard in infant immunization.
- The 23-valent pneumococcal polysaccharide vaccine (PPV23) is recommended for broader serotype coverage in at-risk individuals.
- The use of PPVs, particularly in children, is under ongoing discussion.
Purpose of the Study:
- To review the current evidence on the use of PPV23 in children.
- To assess the benefits and risks of PPV23 in the context of PCV vaccination.
- To explore the implications for protecting at-risk children against pneumococcal infections.
Main Methods:
- Review of existing literature on pneumococcal vaccines.
- Analysis of studies investigating PPV23 efficacy and safety.
- Evaluation of immune responses and potential adverse effects, including B-cell dynamics.
Main Results:
- PPV23 shows limited impact on pneumococcal carriage but may provide some protection against invasive pneumococcal disease (IPD).
- A theoretical risk of memory B-cell depletion exists for PCV serotypes after PPV23 vaccination, especially with revaccination.
- The clinical significance of this B-cell depletion in PCV-primed children is currently unknown.
Conclusions:
- The clinical benefit of PPV23 in at-risk children hinges on age, comorbidities, and serotype immunogenicity.
- The potential for PPV23-induced memory B-cell depletion raises concerns about maintaining optimal protection in susceptible children.
- Further research is needed to clarify the best strategies for sustained protection against IPD in at-risk populations.
Purpose Of Review:
Pneumococcal glycoconjugate vaccines (PCVs) are now widely used in infant immunization schedules. These vaccines are also recommended for those at increased risk of pneumococcal infection and to provide optimal serotype coverage to those at increased risk of disease. The 23-valent polysaccharide vaccine (PPV23) is often advised from the second birthday to provide broader serotype coverage. The use of pneumococcal polysaccharide vaccines (PPVs) has in recent years become a topic of much debate, especially for use in children.
Recent Findings:
Although no effect of PPV23 on carriage has been reported, some protection against invasive pneumococcal disease (IPD) is possible. There is a theoretical risk of memory B-cell depletion to PCV serotypes following PPV23 vaccination, even in PCV-primed children, but the clinical significance is currently unknown. This risk is increased by PPV23 revaccination.
Summary:
Whether the immune response to PPV23, non-PCV13 serotypes is sufficient to confer clinical benefit to at-risk children depends on their age, underlying disease and the immunogenicity of individual serotypes. Given the theoretical risk of memory B-cell depletion following PPV23 vaccination, it is not clear how best to maintain protection in those at-risk children who remain susceptible to IPD.
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