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首页> 外文期刊>Clinical and vaccine immunology: CVI >Optimization and application of a multiplex bead-based assay to quantify serotype-specific IgG against Streptococcus pneumoniae polysaccharides: response to the booster vaccine after immunization with the pneumococcal 7-valent conjugate vaccine.
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Optimization and application of a multiplex bead-based assay to quantify serotype-specific IgG against Streptococcus pneumoniae polysaccharides: response to the booster vaccine after immunization with the pneumococcal 7-valent conjugate vaccine.

机译:优化和应用程序的多路复用量化serotype-specific bead-based化验免疫球蛋白对肺炎链球菌多糖:应对助推器疫苗在免疫接种肺炎球菌7价结合疫苗。

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摘要

We describe the optimization and application of a multiplex bead-based assay (Luminex) to quantify antibodies against polysaccharides of 13 pneumococcal serotypes. In the optimized multiplex immunoassay (MIA), intravenous immune globulin was introduced as an in-house reference serum, and nonspecific reacting antibodies were adsorbed with the commercial product pneumococcal C polysaccharides Multi. The antibody concentrations were assessed in 188 serum samples obtained pre- and post-booster vaccination at 11 months after administration of a primary series of the pneumococcal seven-valent conjugate vaccine (PCV-7) at 2, 3, and 4 months of age. The results of the MIA were compared with those of the ELISA for the serotypes included in the seven-valent conjugated polysaccharide vaccine and for a non-vaccine serotype, serotype 6A. The geometric mean concentrations of the antibodies determined by MIA were slightly higher than those determined by ELISA. The correlations between the assays were good, with R(2) values ranging from 0.84 to 0.91 for all serotypes except serotype 19F, for which R(2) was 0.70. The concentrations of antibody against serotype 6A increased after the administration of PCV-7 due to cross-reactivity with serotype 6B. The differences between the results obtained by ELISA and MIA suggest that the internationally established protective threshold of 0.35 microg/ml should be reevaluated for use in the MIA and may need to be amended separately for each serotype.
机译:我们描述的优化和应用多路复用bead-based化验(Luminex)来量化多糖抗体的13肺炎链球菌血清型。多路复用免疫测定(MIA),静脉注射免疫球蛋白被引入作为一个内部参考血清和非特异性的抗体反应吸附与肺炎球菌的商业产品C多糖多。浓度在188份血清样本进行评估预处理和post-booster获得疫苗接种11点个月后政府的主要系列肺炎球菌seven-valent共轭疫苗(PCV-7) 2、3、4个月大的时候。米娅与比较的结果中包含的血清型的ELISAseven-valent共轭多糖疫苗对于非疫苗血清型血清型6。几何平均浓度的抗体由米娅略高于决定由ELISA。化验是好的,从R(2)值0.84 - 0.91为所有除了血清型血清型19 f R(2)为0.70。抗体的血清型6后增加PCV-7由于管理工作大与血清型6 b。通过ELISA结果之间的差异和米娅建议国际建立保护阈值为0.35microg /毫升应该重新评估使用米娅和可能需要单独修改每一个血清型。

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