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本文引用的文献

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Challenges in the evaluation and licensing of new pneumococcal vaccines, 7-8 July 2008, Ottawa, Canada.2008年7月7 - 8日于加拿大渥太华举行的新型肺炎球菌疫苗评估与许可发放方面的挑战
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Invasive pneumococcal disease in the Netherlands: Syndromes, outcome and potential vaccine benefits.荷兰侵袭性肺炎球菌疾病:综合征、结局及潜在疫苗效益
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Immune response in infants to the heptavalent pneumococcal conjugate vaccine against vaccine-related serotypes 6A and 19A.婴儿对七价肺炎球菌结合疫苗针对疫苗相关血清型6A和19A的免疫反应。
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4
Simultaneous detection of Haemophilus influenzae type b polysaccharide-specific antibodies and Neisseria meningitidis serogroup A, C, Y, and W-135 polysaccharide-specific antibodies in a fluorescent-bead-based multiplex immunoassay.基于荧光微球的多重免疫测定法同时检测b型流感嗜血杆菌多糖特异性抗体和A、C、Y及W-135群脑膜炎奈瑟菌多糖特异性抗体。
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Competitive inhibition flow analysis assay for the non-culture-based detection and serotyping of pneumococcal capsular polysaccharide.用于肺炎球菌荚膜多糖非培养法检测和血清分型的竞争性抑制流动分析测定法
Clin Vaccine Immunol. 2009 Feb;16(2):222-9. doi: 10.1128/CVI.00292-08. Epub 2008 Dec 17.
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Purification and structure characterization of the active component in the pneumococcal 22F polysaccharide capsule used for adsorption in pneumococcal enzyme-linked immunosorbent assays.用于肺炎球菌酶联免疫吸附测定吸附的肺炎球菌22F多糖荚膜中活性成分的纯化及结构表征
Vaccine. 2007 Aug 29;25(35):6490-500. doi: 10.1016/j.vaccine.2007.06.034. Epub 2007 Jul 5.
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Functional antibodies elicited by two heptavalent pneumococcal conjugate vaccines in the Finnish Otitis Media Vaccine Trial.两种七价肺炎球菌结合疫苗在芬兰中耳炎疫苗试验中引发的功能性抗体。
Infect Immun. 2007 Apr;75(4):1794-800. doi: 10.1128/IAI.01673-06. Epub 2007 Jan 29.
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Immunogenicity and boosting after a reduced number of doses of a pneumococcal conjugate vaccine in infants and toddlers.婴幼儿接种减少剂量肺炎球菌结合疫苗后的免疫原性及加强免疫效果
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The five-parameter logistic: a characterization and comparison with the four-parameter logistic.五参数逻辑斯蒂模型:一种特征描述及与四参数逻辑斯蒂模型的比较
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Development and validation of a nonaplex assay for the simultaneous quantitation of antibodies to nine Streptococcus pneumoniae serotypes.一种用于同时定量检测针对九种肺炎链球菌血清型抗体的九联检测法的开发与验证。
J Immunol Methods. 2005 Jan;296(1-2):135-47. doi: 10.1016/j.jim.2004.11.006. Epub 2004 Dec 8.

一种基于多重微珠检测法定量针对肺炎链球菌多糖的血清型特异性IgG的方法的优化与应用:接种7价肺炎球菌结合疫苗后对加强疫苗的反应

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.

作者信息

Elberse Karin E M, Tcherniaeva Irina, Berbers Guy A M, Schouls Leo M

机构信息

Laboratory for Infectious Diseases and Perinatal Screening, National Institute for Public Health and the Environment, Antonie van Leeuwenhoeklaan 9, Bilthoven 3721 MA, Netherlands.

出版信息

Clin Vaccine Immunol. 2010 Apr;17(4):674-82. doi: 10.1128/CVI.00408-09. Epub 2010 Feb 3.

DOI:10.1128/CVI.00408-09
PMID:20130129
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2849341/
Abstract

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.

摘要

我们描述了一种基于多重微珠的检测方法(Luminex)的优化及应用,用于定量检测针对13种肺炎球菌血清型多糖的抗体。在优化的多重免疫分析(MIA)中,引入静脉注射免疫球蛋白作为内部参考血清,并用商业产品肺炎球菌C多糖混合物吸附非特异性反应抗体。在188份血清样本中评估抗体浓度,这些样本是在2、3、4月龄接种肺炎球菌七价结合疫苗(PCV-7)基础免疫系列后11个月进行加强免疫前和加强免疫后采集的。将MIA的结果与酶联免疫吸附测定(ELISA)针对七价结合多糖疫苗中包含的血清型以及非疫苗血清型6A的结果进行比较。MIA测定的抗体几何平均浓度略高于ELISA测定的浓度。除19F血清型外,所有血清型的两种检测方法之间的相关性良好,R²值在0.84至0.91之间,19F血清型的R²值为0.70。由于与6B血清型的交叉反应,PCV-7接种后针对6A血清型的抗体浓度增加。ELISA和MIA所得结果之间的差异表明,国际上确定的0.35μg/ml的保护性阈值应重新评估以用于MIA,并且可能需要针对每种血清型分别进行修正。