Validation of the World Health Organization Enzyme-Linked Immunosorbent Assay for the Quantitation of Immunoglobulin G Serotype-Specific Anti-Pneumococcal Antibodies in Human Serum.
10.3346/jkms.2017.32.10.1581
- Author:
Hyunju LEE
1
;
Soo Young LIM
;
Kyung Hyo KIM
Author Information
1. Department of Pediatrics, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
- Publication Type:Validation Studies ; Original Article
- Keywords:
Streptococcus pneumoniae;
Antibodies;
Enzyme-Linked Immunosorbent Assay;
Validation Studies
- MeSH:
Antibodies*;
Calibration;
Enzyme-Linked Immunosorbent Assay;
Global Health*;
Humans*;
Immunoglobulin G*;
Immunoglobulins*;
Korea;
Pneumococcal Vaccines;
Sensitivity and Specificity;
Seoul;
Serogroup;
Streptococcus pneumoniae;
World Health Organization*
- From:Journal of Korean Medical Science
2017;32(10):1581-1587
- CountryRepublic of Korea
- Language:English
-
Abstract:
The World Health Organization (WHO) enzyme-linked immunosorbent assay (ELISA) guideline is currently accepted as the gold standard for the evaluation of immunoglobulin G (IgG) antibodies specific to pneumococcal capsular polysaccharide. We conducted validation of the WHO ELISA for 7 pneumococcal serotypes (4, 6B, 9V, 14, 18C, 19F, and 23F) by evaluating its specificity, precision (reproducibility and intermediate precision), accuracy, spiking recovery test, lower limit of quantification (LLOQ), and stability at the Ewha Center for Vaccine Evaluation and Study, Seoul, Korea. We found that the specificity, reproducibility, and intermediate precision were within acceptance ranges (reproducibility, coefficient of variability [CV] ≤ 15%; intermediate precision, CV ≤ 20%) for all serotypes. Comparisons between the provisional assignments of calibration sera and the results from this laboratory showed a high correlation > 94% for all 7 serotypes, supporting the accuracy of the ELISA. The spiking recovery test also fell within an acceptable range. The quantification limit, calculated using the LLOQ, for each of the serotypes was 0.05–0.093 μg/mL. The freeze-thaw stability and the short-term temperature stability were also within an acceptable range. In conclusion, we showed good performance using the standardized WHO ELISA for the evaluation of serotype-specific anti-pneumococcal IgG antibodies; the WHO ELISA can evaluate the immune response against pneumococcal vaccines with consistency and accuracy.
