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Opsonophagocytic Killing Assay to Assess Immunological Responses Against Bacterial Pathogens
Published on: April 5, 2019
Pneumococcal serotype-specific IgG and opsonophagocytic activity in young Japanese patients with asplenia
Kenichi Takeshita1,2, Noriko Takeuchi2, Yoshiko Takahashi3
1Department of Pediatrics, Graduate School of Medicine, Chiba University, Chiba-shi, Japan.
Insights
Young patients with asplenia show insufficient immunity against pneumococcal serotypes after vaccination. Those receiving only the pneumococcal polysaccharide vaccine (PPSV23) had weaker responses than those vaccinated with the pneumococcal conjugate vaccine (PCV13).
Area of Science:
- Immunology
- Vaccinology
- Pediatrics
Background:
- Patients with asplenia face a high risk of severe infections from encapsulated bacteria, particularly Streptococcus pneumoniae.
- Pneumococcal conjugate vaccine (PCV13) and pneumococcal polysaccharide vaccine (PPSV23) are recommended for preventing invasive pneumococcal disease.
- Immune responses to pneumococcal vaccines in young asplenic patients remain understudied.
Purpose of the Study:
- To evaluate pneumococcal serotype-specific IgG levels and opsonophagocytic activity in young patients with asplenia.
- To compare immune responses between patients who received PCV13 and those who received only PPSV23.
Main Methods:
- Measurement of pneumococcal serotype-specific IgG (Pn-IgG) and opsonophagocytic activity (Pn-OPA) against selected PCV13 serotypes.
- Analysis of serum samples from 23 young patients with asplenia, some of whom had received PCV13 or PPSV23.
- Comparison of immune markers between vaccination groups, considering the time elapsed since the last vaccine dose.
Main Results:
- Overall Pn-IgG geometric mean concentrations (GMCs) were below those of healthy controls, despite being above cutoff levels.
- Patients vaccinated only with PPSV23 exhibited significantly lower Pn-IgG GMCs against four serotypes compared to those who received PCV13.
- Patients vaccinated only with PPSV23 showed significantly lower Pn-OPA geometric mean titers (GMTs) against three serotypes compared to those who received PCV13.
Conclusions:
- Young patients with asplenia may have insufficient immunity against certain PCV13 pneumococcal serotypes.
- Vaccination strategies involving PCV13 appear to elicit a more robust immune response than PPSV23 alone in this population.
- Further research and appropriate vaccination schedules are needed to ensure adequate protection in young asplenic patients in the post-PCV13 era.
Abstract:
Patients with asplenia are at high risks of severe infections caused by encapsulated bacteria, particularly Streptococcus pneumoniae. Thirteen-valent pneumococcal conjugate vaccine (PCV13) and 23-valent pneumococcal polysaccharide vaccine (PPSV23) are recommended for invasive pneumococcal disease prevention; however, little is known about the immunity to pneumococci in young patients with asplenia. We measured pneumococcal serotype-specific IgG (Pn-IgG) levels and pneumococcal opsonophagocytic activity (Pn-OPA) against some PCV13-contained serotypes (1, 3, 5, 6A, 7 F, 19A) in 23 young patients with asplenia using surplus serum samples. In this study, 5 and 13 patients had received PCV13 during routine immunizations and PPSV23, respectively; however, >5 years had passed since the last dose in most cases. The geometric mean concentrations (GMCs) of Pn-IgG in all study patients were not under the cutoff level against six serotypes, but they were lower than the those of age-matched healthy controls, as we have previously published. The patients who had received only PPSV23 had significantly lower GMCs against four serotypes (serotypes 1, 6A, 7 F, and 19A) than that of the patients who had received at least one PCV13 vaccination. The patients who had received only PPSV23 also had significantly lower geometric mean titers (GMTs) of Pn-OPA against all three serotypes we measured (serotypes 3, 5, and 19A) than that of the patients who had received at least one PCV13 vaccination. Our findings are useful data that can indicate insufficient immunity in young patients with asplenia against some PCV13 pneumococci serotypes and suggest the need for appropriate vaccinations in the post-PCV13 era.
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