首页> 美国卫生研究院文献>Clinical and Diagnostic Laboratory Immunology >Comparative Study of Different Sources of Pertussis Toxin (PT) as Coating Antigens in IgG Anti-PT Enzyme-Linked Immunosorbent Assays
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Comparative Study of Different Sources of Pertussis Toxin (PT) as Coating Antigens in IgG Anti-PT Enzyme-Linked Immunosorbent Assays

机译:IgG抗PT酶联免疫吸附法中不同来源百日咳毒素(PT)包被抗原的比较研究

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摘要

In an effort to improve the reliability and reproducibility of serological assays for Bordetella pertussis, a collaborative study was conducted to compare four different sources of pertussis toxin (PT) as coating antigens in the immunoglobulin G (IgG) anti-PT enzyme-linked immunosorbent assay (ELISA). Four sources of PT were used as coating antigens in the IgG anti-PT ELISA in four different testing laboratories (labs A to D) to determine whether the different antigen preparations and different laboratories influenced assay results. A panel of 60 sera consisting of deidentified human specimens from previous vaccination trials of healthy adults and infants and clinical specimens from outbreak settings was tested. In the four laboratories, each sample was tested three times with the four PT antigens according to the standard coating optimization and IgG anti-PT ELISA testing procedures used in that laboratory. Differences among the antigens, as well as intra- and interlaboratory variability, were evaluated. Excellent agreement was observed with the test panel results among the four antigens within each laboratory. Concordance correlation coefficient (rc) measurements among the different antigens ranged from 0.99, 0.99 to 1.00, 1.00, and 0.97 to 1.00 for labs A to D, respectively. The comparisons between pairs of laboratories also indicated a high degree of concordance for each PT preparation, with rc measurements between 0.90 and 0.98, 0.93 and 0.99, 0.92 and 0.98, and 0.93 and 0.99 for antigens 1 to 4, respectively. Relatively minor differences in results were observed among laboratories or among antigens, suggesting that the four PT antigens are quite similar and could be considered for acceptance in harmonized immunoassays used for serodiagnosis or vaccine evaluation.
机译:为了提高百日咳博德特氏菌血清学检测的可靠性和可重复性,开展了一项合作研究,比较了四种不同来源的百日咳毒素(PT)作为免疫球蛋白G(IgG)抗PT酶联免疫吸附测定中的包被抗原(ELISA)。在四个不同的测试实验室(实验室A至D)中,将四种PT来源用作IgG抗PT ELISA的包被抗原,以确定不同的抗原制剂和不同的实验室是否影响测定结果。测试了一组60份血清,其中包括来自先前对健康成人和婴儿进行的疫苗接种试验的身份不明的人类标本和来自爆发场所的临床标本。在四个实验室中,根据该实验室使用的标准包被优化和IgG抗PT ELISA测试程序,对每种样品用四种PT抗原进行了三次测试。评价了抗原之间的差异以及实验室内和实验室间的变异性。在每个实验室中,四种抗原之间的测试结果均显示出极好的一致性。对于实验室A到D,不同抗原之间的一致性相关系数(rc)测量值分别为0.99、0.99至1.00、1.00和0.97至1.00。实验室对之间的比较也表明每种PT制剂具有高度的一致性,抗原1-4的rc值分别在0.90和0.98、0.93和0.99、0.92和0.98、0.93和0.99之间。在实验室之间或抗原之间观察到相对较小的结果差异,表明四种PT抗原非常相似,可以考虑用于血清学诊断或疫苗评估的统一免疫测定中。

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