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Updated: Jun 15, 2026

Experimental Human Pneumococcal Carriage
Published on: February 15, 2013
Hyporesponsiveness to re-challenge dose following pneumococcal polysaccharide vaccine at 12 months of age, a
F M Russell1, J R Carapetis, A Balloch
1Centre for International Child Health, Department of Paediatrics, University of Melbourne, Royal Children's Hospital, Melbourne, Victoria, Australia. fmruss@unimelb.edu.au
Insights
Giving infants the 23-valent pneumococcal polysaccharide vaccine (23vPPS) at 12 months impaired their immune response to a later pneumococcal conjugate vaccine (PCV) challenge. This suggests a suboptimal vaccination strategy for pneumococcal protection in infants.
Area of Science:
- Immunology
- Vaccinology
- Pediatrics
Background:
- Evaluating the immunological impact of the 23-valent pneumococcal polysaccharide vaccine (23vPPS) in infants previously vaccinated with the 7-valent pneumococcal conjugate vaccine (PCV).
- Assessing the effect of varying PCV infant doses on the response to a subsequent 23vPPS challenge.
Purpose of the Study:
- To determine the immunological consequences of administering 23vPPS at 12 months in infants with different infant PCV vaccination histories.
- To analyze the impact of 23vPPS on the immune response to a subsequent pneumococcal polysaccharide vaccine (mPPS) challenge.
Main Methods:
- A randomized trial involving 552 Fijian infants stratified by ethnicity.
- Infants received zero, one, two, or three PCV doses, followed by either 23vPPS or no vaccine at 12 months.
- All infants received a small dose of 23vPPS (mPPS) at 17 months, with serum samples collected pre- and post-vaccination.
Main Results:
- Antibody concentrations were higher at 17 months in infants who received 23vPPS at 12 months.
- However, infants who did *not* receive the 12-month 23vPPS showed a significantly higher antibody response to the mPPS challenge for all PCV serotypes.
- A prior 23vPPS dose at 12 months was associated with a diminished immune response to the subsequent mPPS challenge across all 23 serotypes.
Conclusions:
- While 23vPPS at 12 months boosts antibody levels, it impairs the immune system's ability to respond effectively to a subsequent pneumococcal vaccine challenge.
- This finding suggests that the timing and sequence of pneumococcal vaccines (PCV and 23vPPS) significantly influence infant immune responses and may necessitate strategy adjustments.
Background:
To evaluate the immunological impact of the 23-valent pneumococcal polysaccharide vaccine (23vPPS) at 12 months, for children who have received zero to three infant doses of seven-valent pneumococcal conjugate vaccine (PCV), on responses to a subsequent exposure to a small dose of 23vPPS (mPPS).
Methods:
Five hundred and fifty-two Fijian infants were stratified by ethnicity and randomized into eight groups to receive zero, one, two, or three PCV doses at 14 weeks, six and 14 weeks, or six, ten, and 14 weeks. Within each group, half received 23vPPS at 12 months and all received mPPS at 17 months. Sera were taken prior and one month post-mPPS.
Findings:
By 17 months, geometric mean antibody concentrations (GMC) to all 23 serotypes in 23vPPS were significantly higher in children who had received 23vPPS at 12 months compared to those who had not. Post-mPPS, children who had not received the 12 month 23vPPS had a significantly higher GMC for all PCV serotypes compared with those who had (each p<0.02). For the non-PCV serotypes, children who had not received the 12 month 23vPPS had significantly higher GMC for six of 16 non-PCV serotypes (7F, 9N, 12F, 19A, 22F, 33F) than those who did (each p<0.02). After adjusting for the pre-mPPS level, exposure to 23vPPS was associated with a lower response to mPPS for all serotypes (each p<0.001).
Interpretation:
Despite higher antibody concentrations at 17 months in children who had received 23vPPS at 12 months, the response to a re-challenge was poor for all 23 serotypes compared to children who had not received the 12 month 23vPPS.
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