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Updated: May 12, 2026

Experimental Human Pneumococcal Carriage
Published on: February 15, 2013
Invasive pneumococcal disease among infants before and after introduction of pneumococcal conjugate vaccine
Katherine A Poehling1, Thomas R Talbot, Marie R Griffin
1Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN 37232-2504, USA. katherine.poehling@vanderbilt.edu
Insights
The heptavalent pneumococcal conjugate vaccine (PCV7) significantly reduced invasive pneumococcal disease (IPD) rates in infants under 90 days old by 40%. This vaccine also eliminated previous racial disparities in IPD rates among infants.
Area of Science:
- Pediatric Infectious Diseases
- Vaccinology
- Epidemiology
Background:
- Streptococcus pneumoniae poses a significant health risk to young infants.
- The heptavalent pneumococcal conjugate vaccine (PCV7) was introduced in 2000 for children aged 2-23 months.
Purpose of the Study:
- To evaluate the impact of PCV7 introduction on invasive pneumococcal disease (IPD) rates in infants younger than 90 days.
- To assess changes in IPD incidence before and after the vaccine's incorporation into the routine immunization schedule.
Main Methods:
- A prospective, population-based study was conducted in 8 US states from July 1997 to June 2004.
- Laboratory surveillance data for invasive S. pneumoniae infections in infants aged 0-90 days were analyzed.
- IPD rates were compared before (1997-2000) and after (2001-2004) PCV7 introduction, excluding a transition year.
Main Results:
- Overall IPD rates in infants aged 0-90 days decreased by 40%, from 11.8 to 7.2 per 100,000 live births.
- Rates of IPD significantly decreased among black infants (from 17.1 to 5.3 per 100,000), eliminating previous racial disparities.
- Incidence of PCV7-serotype IPD dropped significantly, while non-PCV7 serotypes remained stable.
Conclusions:
- PCV7 introduction has led to a significant decline in IPD rates among young infants.
- The vaccine's impact extends to infants too young to be vaccinated, likely through reduced pathogen carriage in the community.
- PCV7 vaccination has successfully addressed and eliminated racial disparities in IPD incidence among infants.
Context:
Streptococcus pneumoniae is a serious infection in young infants. A heptavalent pneumococcal conjugate vaccine (PCV7) was licensed in 2000 and recommended for all children aged 2 to 23 months.
Objective:
To determine the rates of invasive pneumococcal disease (IPD) in young infants before and after PCV7 was incorporated into the childhood immunization schedule in June 2000.
Design, Setting, And Participants:
A prospective, population-based study of infants aged 0 to 90 days who resided in areas in 8 US states with active laboratory surveillance for invasive S pneumoniae infections from July 1, 1997, to June 30, 2004.
Main Outcome Measures:
Rates of laboratory-confirmed IPD before (July 1, 1997-June 30, 2000) and after (July 1, 2001-June 30, 2004) PCV7 introduction, excluding a transition year (July 1, 2000-June 30, 2001).
Results:
There were 146 cases of IPD, 89 before and 57 after PCV7 introduction. Isolated bacteremia occurred in 94 cases (64%), pneumonia in 27 (18%), meningitis in 22 (15%), and septic arthritis and/or osteomyelitis in 3 (2%). Mean rates of IPD for infants aged 0 to 90 days decreased 40% from 11.8 (95% confidence interval [CI], 9.6-14.5) to 7.2 (95% CI, 5.6-9.4; P = .004) per 100 000 live births following PCV7 introduction. Among black infants, mean rates of IPD decreased significantly from 17.1 (95% CI, 11.9-24.6) to 5.3 (95% CI, 2.8-10.1; P = .001) per 100,000 live births, with a nonsignificant decrease from 9.6 (95% CI, 7.3-12.7) to 6.8 (95% CI, 4.9-9.4) per 100,000 live births for white infants. Rates of PCV7-serotype isolates decreased significantly from 7.3 (95% CI, 5.3-10.1) to 2.4 (95% CI, 1.6-3.8; P<.001) per 100,000 live births, while rates of non-PCV7 serotypes remained stable (P = .55).
Conclusions:
Since PCV7 introduction, rates of IPD in young infants have decreased significantly, providing evidence that vaccinating children aged 2 to 23 months has led to changes in pneumococcal carriage in infants too young to receive PCV7. With a significant decrease in rates of IPD among black infants, the previous racial difference has been eliminated.
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