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Updated: Feb 7, 2026

Experimental Human Pneumococcal Carriage
Published on: February 15, 2013
Dynamic transmission modelling to address infant pneumococcal conjugate vaccine schedule modifications in the UK
M Wasserman1, A Lucas2, D Jones3
1Pfizer Inc.,New York, NY,USA.
Insights
The UK
Area of Science:
- Immunology
- Epidemiology
- Public Health
Background:
- The UK utilizes a 2+1 schedule for the 13-valent pneumococcal conjugate vaccine (PCV) since 2010.
- A shift to a 1+1 schedule is recommended, but the impact on pneumococcal disease burden remains uncertain.
Purpose of the Study:
- To model the potential increase in pneumococcal disease and deaths following a switch to a 1+1 PCV schedule in the UK.
- To identify factors influencing pneumococcal disease resurgence under a 1+1 schedule.
Main Methods:
- A dynamic transmission model was developed to simulate pneumococcal disease spread.
- The model predicted disease cases and deaths over a 5-year period under a 1+1 schedule.
Main Results:
- A 1+1 schedule is predicted to cause 8777-27,807 additional disease cases and 241-743 deaths over 5 years.
- Serotype 19A is projected to account for 55-71% of new invasive pneumococcal disease (IPD) cases.
- Booster adherence, vaccine effectiveness against carriage, and waning immunity significantly influence disease resurgence.
Conclusions:
- Switching to a 1+1 PCV schedule is likely to substantially increase overall pneumococcal disease burden in the UK.
- Current model predictions may be conservative, given recent increases in IPD caused by vaccine serotypes.
Abstract:
The 13-valent pneumococcal conjugate vaccine (PCV) has been part of routine immunisation in a 2 + 1 schedule (two primary infant doses and one booster during the second year of life) in the UK since 2010. Recently, the UK's Joint Committee on Vaccination and Immunisation recommended changing to a 1 + 1 schedule while conceding that this will increase disease burden; however, uncertainty remains on how much pneumococcal burden - including invasive pneumococcal disease (IPD) and non-invasive disease - will increase. We built a dynamic transmission model to investigate this question. The model predicted that a 1 + 1 schedule would incur 8777-27 807 additional cases of disease and 241-743 more deaths over 5 years. Serotype 19A caused 55-71% of incremental IPD cases. Scenario analyses showed that booster dose adherence, effectiveness against carriage and waning in a 1 + 1 schedule had the most influence on resurgence of disease. Based on the model assumptions, switching to a 1 + 1 schedule will substantially increase disease burden. The results likely are conservative since they are based on relatively low vaccine-type pneumococcal transmission, a paradigm that has been called into question by data demonstrating an increase of IPD due to several vaccine serotypes during the last surveillance year available.
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