Predicting the Epidemiological Effects in the United Kingdom of Moving from PCV13 to PCV15 in the Routine Pediatric 1

Rachel J Oidtman1, Natalie Banniettis1, Jessica Weaver1

  • 1Merck & Co., Inc., Rahway, NJ 07065, USA.

Vaccines
|June 27, 2025
PubMed

Insights

Switching to pneumococcal conjugate vaccine 15 (PCV15) from PCV13 in the UK pediatric National Immunization Programme (NIP) with a 1+1 schedule is projected to lower invasive pneumococcal disease (IPD) incidence in children and the overall population.

Area of Science:

  • Immunology
  • Epidemiology
  • Public Health

Background:

  • Pneumococcal conjugate vaccines (PCVs) significantly reduced invasive pneumococcal disease (IPD) in the UK pediatric National Immunization Programme (NIP) since 2006.
  • The UK NIP shifted to a 1+1 pediatric PCV dosing schedule in 2020, reducing doses from 2+1.

Purpose of the Study:

  • To evaluate the public health impact of using PCV15 versus PCV13 under the current 1+1 pediatric dosing schedule.
  • To compare the effectiveness of PCV15 and PCV13 in reducing IPD incidence over a 20-year period.

Main Methods:

  • A UK-adapted population-level compartmental model was utilized to simulate IPD incidence.
  • Probabilistic sensitivity analysis assessed uncertainty in vaccine efficacy (VE) for PCV13 and PCV15 under the 1+1 schedule, assuming 0-24% lower VE than the 2+1 schedule.
  • The model projected outcomes over a 20-year time horizon.

Main Results:

  • Under the 1+1 schedule, PCV15 vaccination resulted in a 3.5% increase in IPD incidence in children <2 years old, compared to an 11.1% increase with PCV13.
  • Over 20 years, PCV15 is predicted to yield a 6.0% lower overall IPD incidence than PCV13 (10.70 vs. 11.38 cases per 100,000 population).

Conclusions:

  • Transitioning from PCV13 to PCV15 for routine pediatric vaccination in the UK, using a 1+1 schedule, is associated with reduced IPD incidence.
  • PCV15 demonstrates superior effectiveness in lowering IPD rates in both pediatric and the general population compared to PCV13 under the 1+1 dosing strategy.
Abstract