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Experimental Human Pneumococcal Carriage
Published on: February 15, 2013
Effectiveness of 7- and 13-Valent Pneumococcal Conjugate Vaccines in a Schedule Without a Booster Dose: A 10-Year
Sanjay Jayasinghe1, Clayton Chiu1, Helen Quinn1
1National Centre for Immunisation Research and Surveillance for Vaccine Preventable Diseases, Westmead and Discipline of Child and Adolescent Health, Medical School, University of Sydney, Sydney, Australia.
Insights
Australia
Area of Science:
- Public Health
- Vaccinology
- Epidemiology
Background:
- Australia's unique infant pneumococcal conjugate vaccine (PCV) schedule uses 3 primary doses without a booster (3+0).
- This schedule initially utilized 7-valent PCV (PCV7) from 2005, transitioning to 13-valent PCV (PCV13) in 2011.
- Vaccine effectiveness (VE) and waning were assessed for both PCV7 and PCV13 under this schedule.
Purpose of the Study:
- To measure the vaccine effectiveness (VE) of PCV7 and PCV13 in Australia using a 3+0 infant schedule.
- To evaluate the waning of protection offered by these vaccines over time.
- To determine if a booster dose is necessary to maintain protection against invasive pneumococcal disease (IPD).
Main Methods:
- Utilized a case-control study design with IPD notifications and age-matched controls from the Australian Childhood Immunisation Register.
- Employed an indirect cohort method using IPD cases from non-vaccine serotypes as controls.
- Calculated VE using logistic regression and assessed waning by examining the odds of vaccine-type IPD in the 12-36 months post-primary vaccination period.
Main Results:
- Both PCV7 and PCV13 demonstrated high initial VE in infants: 92.9% for PCV7 and 86.5% for PCV13.
- A significant increase in the odds of vaccine-type IPD was observed from 12 months post-dose 3, indicating waning protection.
- Waning occurred for both PCV7 and PCV13, with odds of IPD increasing significantly by 24-36 months post-vaccination.
Conclusions:
- The 3+0 infant PCV schedule, while initially effective, shows progressive increases in breakthrough invasive pneumococcal disease (IPD) cases post-PCV13.
- Waning immunity suggests that the current 3+0 schedule may not provide sustained protection.
- A booster dose of PCV13 in the second year of life is recommended to maintain protection against IPD.
Background:
Unique among high-income countries, Australia has used a 3 + 0 schedule (3 primary doses, no booster) for infant pneumococcal conjugate vaccine (PCV) since January 2005, initially 7 valent (PCV7) then 13 valent (PCV13) from July 2011. We measured vaccine effectiveness (VE) of both PCVs against invasive pneumococcal disease (IPD) using 2 methods.
Methods:
Cases were IPD notifications to the national surveillance system of children eligible for respective PCVs. For case-control method, up to 10 age-matched controls were derived from the Australian Childhood Immunisation Register. For indirect cohort method, controls were IPD cases due to serotypes not in PCVs. VE was calculated as (1 - odds ratio [OR]) × 100 by logistic regression. VE waning was estimated as odds of vaccine type (VT) IPD in consecutive 12-month periods post-dose 3.
Results:
Between 2005 and 2014, there were 1209 and 308 IPD cases in PCV7-eligible and PCV13-eligible cohorts, respectively. Both methods gave comparable VE estimates. In infants, VE for 3 doses against VT IPD was 92.9% (95% confidence interval [CI], 27.7% to 99.3%) for PCV7 and 86.5% (95% CI, 11.7% to 97.9%) for PCV13. From 12 months post-dose 3, the odds of VT IPD by 24-36 months increased significantly for PCV7 (5.6, 95% CI, 1.2-25.4) and PCV13 (5.9, 95% CI, 1.0-35.2).
Conclusions:
For both PCVs in a 3 + 0 schedule, despite similar VE, progressive increase in breakthrough cases only occurred post-PCV13. This supports the importance of a booster dose of PCV13 in the second year of life to maintain protection.
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