What is the preventive effectiveness of Prevnar 13 (Pneumococcal conjugate vaccine) in preventing pneumonia?

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Last updated: September 16, 2025View editorial policy

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Preventive Effectiveness of Prevnar 13 in Preventing Pneumonia

Prevnar 13 (PCV13) is highly effective in preventing pneumonia, with a 27% efficacy against chest X-ray-confirmed pneumonia and 6% efficacy against clinical pneumonia in children under 2 years of age. 1

Efficacy Data for Prevnar 13

Prevnar 13 is a 13-valent pneumococcal conjugate vaccine that contains seven serotypes from the earlier PCV7 vaccine (serotypes 4, 6B, 9V, 14, 18C, 19F, and 23F) plus six additional serotypes (1,3,5, 6A, 7F, and 19A). This expanded coverage targets over 85% of epidemiologically important pneumococcal serotypes worldwide. 2

The vaccine's effectiveness against pneumonia has been established through multiple clinical trials:

  • A systematic review by the Cochrane Collaboration analyzed data from five randomized controlled trials involving 113,044 children under 2 years of age. The pooled vaccine efficacy estimates showed:
    • 27% efficacy (95% CI = 15%–36%) against chest X-ray–confirmed pneumonia meeting WHO criteria
    • 6% efficacy (95% CI = 2%–9%) against clinical pneumonia
    • 80% efficacy (95% CI = 58%–90%) against vaccine-type invasive pneumococcal disease (IPD)
    • 58% efficacy (95% CI = 29%–75%) against IPD caused by all serotypes 1

Effectiveness in Different Populations

The vaccine's effectiveness varies across different populations:

  • In HIV-infected children, a 9-valent investigational PCV showed 65% efficacy (95% CI = 24%–86%) against IPD
  • In HIV-uninfected children, the same vaccine showed higher efficacy of 83% (95% CI = 39%–97%) 1
  • Long-term follow-up (6 years) showed that vaccine efficacy against IPD declined substantially in HIV-infected children but remained stable in healthy children 1

Immunogenicity and Safety

PCV13 has demonstrated strong immunogenicity against all 13 pneumococcal serotypes:

  • The vaccine elicits robust immune responses with either a two- or three-dose primary vaccination series in infants aged 2-6 months 3
  • Antibodies produced against all vaccine serotypes are functional, as demonstrated by opsonophagocytic activity 4
  • A booster dose administered between 11-15 months of age generally enhances the immune response against all 13 serotypes 3
  • PCV13 has a safety profile comparable to PCV7, with generally mild reactogenicity 4

Recommendations for Use

Based on its efficacy and safety profile, the Advisory Committee on Immunization Practices (ACIP) recommends:

  1. Routine vaccination of all children aged 2-59 months
  2. Vaccination of children aged 60-71 months with underlying medical conditions
  3. Vaccination of children who received ≥1 dose of PCV7 previously 1

For routine immunization of infants, PCV13 is recommended as a 4-dose series at ages 2,4,6, and 12-15 months. 1

Practical Considerations

When implementing PCV13 vaccination:

  • The vaccine does not interfere with immune responses to other routine pediatric vaccines, making it compatible with standard immunization schedules 3
  • The toddler dose (12-15 months) results in higher immune responses compared to the infant series doses, highlighting the importance of completing the full vaccination schedule 4
  • Catch-up vaccination schedules for older infants and children aged 7-72 months also produce robust immune responses against all serotypes 3

Caveats and Limitations

Important considerations when evaluating PCV13's effectiveness:

  • While the vaccine is highly effective against the included serotypes, it does not protect against all pneumococcal serotypes
  • Efficacy against otitis media is established only for the seven serotypes included in PCV7, with no specific efficacy data available for the six additional serotypes in PCV13 1
  • The vaccine's effectiveness may vary based on regional serotype distribution and prevalence

PCV13 represents a significant advancement in pneumococcal disease prevention, offering broader protection than its predecessor while maintaining a similar safety profile.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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