Prediction of Pneumococcal Conjugate Vaccine Effectiveness against Invasive Pneumococcal Disease Using Opsonophagocytic Activity and Antibody Concentrations Determined by Enzyme-Linked Immunosorbent Assay with 22F Adsorption

被引:36
作者
Schuerman, L. [1 ]
Wysocki, J. [2 ,3 ]
Tejedor, J. C. [4 ]
Knuf, M. [5 ,6 ]
Kim, K. -H. [7 ]
Poolman, J. [1 ]
机构
[1] GlaxoSmithKline Biol, Wavre Rixensart, Belgium
[2] Univ Sch Med Sci, Poznan, Poland
[3] Reg Med Ctr Mother & Child, Poznan, Poland
[4] Hosp Mostoles, Serv Neonatol, Madrid, Spain
[5] Johannes Gutenberg Univ Mainz, Zentrum Kinder & Jugendmed, Mainz, Germany
[6] Childrens Hosp, Dr Horst Schmidt Klin, Wiesbaden, Germany
[7] Ewha Womans Univ, Dept Pediat, Coll Med, Seoul, South Korea
关键词
SEROTYPE; 19A; PHID-CV; UNITED-STATES; IMMUNOGENICITY; CHILDREN; EFFICACY; SAFETY; PROTECTION; SCHEDULE; INFANTS;
D O I
10.1128/CVI.05313-11
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We compared the abilities of two serological readouts, antipolysaccharide IgG antibody concentrations and opsonophagocytic activity (OPA) titers, to predict the clinical effectiveness of the 7-valent pneumococcal conjugate vaccine (7vCRM) against invasive pneumococcal disease (IPD). We also assessed the accuracy of the previously established thresholds for GlaxoSmithKline's enzyme-linked immunosorbent assay with 22F adsorption (22F-ELISA) (>= 0.2 mu g/ml) and OPA assay (titer, >= 8) in predicting effectiveness. We showed that following a 3-dose 7vCRM primary vaccination, the serological response rates as determined using thresholds of >= 0.2 mu g/ml IgG and an OPA titer of >= 8 corresponded well with overall effectiveness against IPD. In addition, the OPA assay seemed to better predict serotype-specific effectiveness than enzyme-linked immunoassay. Finally, when applied to post-dose-2 immune responses, both thresholds also corresponded well with the overall IPD effectiveness following a 2-dose 7vCRM primary vaccination. These results support the importance of the OPA assay in evaluating immune responses to pneumococcal conjugate vaccines.
引用
收藏
页码:2161 / 2167
页数:7
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