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Updated: Feb 3, 2026

Capsular Serotyping of Streptococcus pneumoniae Using the Quellung Reaction
Published on: February 24, 2014
Outpacing the pneumococcus: Antibody dynamics in the first few days following pneumococcal capsular antigen
Sheila Z Kimaro Mlacha1,2, Anne Warira3, Hellen Gatakaa3
1Kenya Medical Research Institute - Wellcome Trust Research Programme, Kilifi, Kenya. shezekimla@gmail.com.
Insights
Children
Area of Science:
- Immunology
- Pediatrics
- Infectious Diseases
Background:
- Children in developing nations face frequent pneumococcus exposure.
- Invasive pneumococcal disease (IPD) is less common than exposure, suggesting host factors influence outcomes.
- Natural variation in immune responses may impact IPD susceptibility.
Purpose of the Study:
- To investigate the natural variation in the speed of immunoglobulin G (IgG) antibody responses to pneumococcal polysaccharides in children.
- To determine if differences in IgG response speed affect susceptibility to or outcomes of invasive pneumococcal disease (IPD).
Main Methods:
- Recruited children aged 24-36 months who had recovered from IPD and age-matched healthy controls.
- Administered a single dose of 23-valent pneumococcal polysaccharide vaccine (PPV) to mimic natural exposure.
- Analyzed serum samples post-vaccination to measure the dynamics of anti-polysaccharide IgG antibody responses to various capsular antigens.
Main Results:
- Mean IgG response times to different pneumococcal serotypes ranged from 6.4 to 7.3 days, with standard deviations indicating a natural response variation of up to 7 days.
- Serotype 1 showed the largest fold-rise in antibodies, while serotype 23F showed the smallest.
- The proportion of children achieving antibody responses by day 7 was similar in both children with a history of IPD and healthy controls.
Conclusions:
- Significant natural variation exists in the rapidity of anti-pneumococcal IgG responses, spanning 4-7 days.
- No evidence suggests that children who have experienced IPD exhibit slower immune responses to pneumococcal antigens compared to healthy children.
- Host immune response dynamics do not appear to be a primary factor differentiating IPD history in this age group.
Abstract:
Children in developing countries are frequently exposed to the pneumococcus, but few develop invasive pneumococcal disease (IPD). We test the hypothesis that natural variation exists in the rapidity of IgG responses following exposure to pneumococcal polysaccharides, and that these differences are sufficiently great to affect susceptibility to and outcome of IPD. We recruited children aged 24-36 months, who had recovered from IPD, and age-matched healthy controls and vaccinated them with 1 dose of the 23-valent PPV to mimic natural exposure. We collected serum samples after vaccination and analysed the dynamics of anti-polysaccharide antibody responses to several capsular antigens. Mean IgG response times to different serotypes were 6.4-7.3 days, with standard deviations of 0.9-1.85 days, suggesting a natural range in response times of up to 7 days. Serotype 1 elicited the largest fold-rise, serotype 23F the smallest. The proportion of responses achieved by day 7 was similar in children with a history of IPD and healthy children. There was considerable natural variation in the rapidity of anti-capsular IgG responses extending over 4-7 days. There was no evidence to suggest that children who have experienced IPD respond more slowly to heterologous pneumococcal capsular antigens than do healthy children.
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