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Capsular Serotyping of Streptococcus pneumoniae Using the Quellung Reaction
Published on: February 24, 2014
Pneumococcal antibodies in a child with type 14 pneumococcal conjugate vaccine failure
Katherine L O'Brien1, Jennifer Moïsi, Sandra Romero-Steiner
1Center for American Indian Health, Johns Hopkins Bloomberg School of Public Health, 621 N, Washington St., Baltimore, MD, United States. klobrien@jhsph.edu
Insights
Antibody levels alone do not predict protection against pneumococcal infections. Functional activity and avidity also vary, indicating immune correlates are population-level insights, not individual guarantees.
Area of Science:
- Immunology
- Vaccinology
- Pediatrics
Background:
- Pneumococcal conjugate vaccines (PnCRM7) are crucial for preventing invasive pneumococcal disease (IPD).
- Understanding individual immune responses post-vaccination is key to assessing vaccine efficacy.
- Serotype 14 invasive pneumococcal disease (IPD) can occur despite vaccination.
Purpose of the Study:
- To investigate antibody concentration, opsonic activity, and avidity in a vaccine failure case.
- To compare immune responses in a patient with serotype 14 pneumococcal bacteremia to controls.
Main Methods:
- Measured serotype-specific serum antibodies (concentration, opsonic activity, avidity) in a PnCRM7 vaccine recipient with IPD.
- Compared antibody characteristics to control groups vaccinated with PnCRM7 or meningococcal conjugate vaccine (MnCC) without IPD.
Main Results:
- The vaccine failure case had high antibody concentration but lower avidity compared to controls.
- Antibodies in the case showed greater opsonic activity than controls.
- The patient did not exhibit a booster response to a subsequent vaccine dose.
Conclusions:
- Individual antibody concentration, opsonic activity, and avidity do not reliably predict protection against IPD.
- Immunological correlates of protection are most meaningful at the population level, not for individual risk assessment.
Abstract:
We measured the concentration, opsonic activity, and avidity of serotype-specific serum antibodies in a pneumococcal conjugate vaccine (PnCRM7) efficacy trial participant who contracted serotype 14 pneumococcal bacteremia following dose 3 of PnCRM7. Controls included 18 PnCRM7- and 10 MnCC-vaccinated children without invasive pneumococcal disease (IPD). The child with vaccine failure had 4.98mcg/mL of serotype 14 antibodies 10 days before disease onset; these antibodies had greater opsonic activity and lower avidity than those of control PnCRM7 recipients. The child had no booster response to a fourth dose of PnCRM7 for most vaccine serotypes. We conclude that antibody concentration, functional activity and avidity do not predict individual protection against IPD, and immunological correlates of protection are only useful at the population level.
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