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Updated: May 11, 2026

Opsonophagocytic Killing Assay to Assess Immunological Responses Against Bacterial Pathogens
Published on: April 5, 2019
Pneumococcal vaccine and opsonic pneumococcal antibody.
Joon Young Song1, M Allen Moseley, Robert L Burton
1Division of Infectious Diseases, Department of Internal Medicine, Korea University College of Medicine, Seoul, Republic of Korea.
The opsonophagocytosis assay (OPA) is a superior measure of pneumococcal vaccine efficacy compared to traditional antibody tests. OPA better reflects protection, especially in challenging populations and situations.
Area of Science:
- Immunology
- Vaccinology
- Microbiology
Background:
- Streptococcus pneumoniae causes significant pneumonia and invasive diseases.
- Pneumococcal conjugate vaccines have reduced disease incidence.
- New vaccine trials cannot use placebos, necessitating surrogate markers for efficacy.
Purpose of the Study:
- To evaluate the opsonophagocytosis assay (OPA) as a surrogate marker for pneumococcal vaccine immunogenicity.
- To compare OPA with traditional antibody level measurements (ELISA).
- To highlight OPA's utility in specific populations and clinical scenarios.
Main Methods:
- Development and technical improvements of the opsonophagocytosis assay (OPA).
- Application of OPA for analyzing small sample volumes, including from children.
- Correlation analysis of OPA results with ELISA in various study groups.
Main Results:
- OPA replicates the in vivo antibody protection mechanism, offering a better reflection of vaccine-induced immunity.
- OPA has been optimized for speed, multiplexing, and small sample analysis.
- While ELISA and OPA correlate well in young children, discrepancies arise in elderly, immunodeficient populations, and with cross-reactive antibodies.
Conclusions:
- OPA serves as a valuable supplementary measure of pneumococcal vaccine immunogenicity, particularly when ELISA shows limitations.
- Standardization efforts are underway to further enhance the applicability and reliability of OPA.
- OPA is crucial for assessing vaccine efficacy in contexts where placebo-controlled trials are not feasible.
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