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.

Scientific Reports
|October 20, 2018
PubMed

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.

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