Marchese Rocio D, Jain Neil T, Antonello Joseph, Mallette Laura, Butterfield-Gerson Kristin L, Raab Jennifer, Burke Pamela, Schulman Cheryl, Adgate Hilary, Sikkema Daniel J, Chirmule Narendra
Vaccine and Biologics Research, Merck Research Laboratories, WYN-1, 466 Devon Park Dr., Wayne, PA 19087-8630, USA.
Clin Vaccine Immunol. 2006 Aug;13(8):905-12. doi: 10.1128/CVI.00014-06.
The Merck pneumococcal (Pn) enzyme-linked immunosorbent assays (ELISAs) for measuring antibodies to 12 serotypes (serotypes 1, 3, 4, 6B, 7F, 8, 9V, 12F, 14, 18C, 19F, and 23F) were validated in 1999. Merck Laboratories developed the Pn assays using 10 microg/ml C polysaccharide, 100 microg/ml Pn polysaccharide (PnPs) 25, and 100 microg/ml PnPs 72 for preadsorption of samples, standards, and controls in order to improve the specificity to the Pn serotypes in the vaccine. The Pn assays utilize postimmunization sera obtained from subjects immunized with PNEUMOVAX 23 as standards for measuring immunoglobulin G concentrations in sera obtained from vaccine clinical trials with adults and infants. This material was calibrated to the Pn reference standard serum, 89SF, subjected to the Merck Pn ELISA adsorbants. Comparisons were made between the Merck Pn assay and the international Pn assay, showing moderate agreement between the two assay formats. This work describes the test procedures and operating characteristics of the Merck Pn assays and the results of experiments performed to compare the Merck Pn ELISAs to the international Pn ELISAs.
默克公司用于检测针对12种血清型(血清型1、3、4、6B、7F、8、9V、12F、14、18C、19F和23F)抗体的肺炎球菌(Pn)酶联免疫吸附测定(ELISA)于1999年得到验证。默克实验室开发的Pn测定法使用10微克/毫升的C多糖、100微克/毫升的Pn多糖(PnPs)25和100微克/毫升的PnPs 72对样品、标准品和对照进行预吸附,以提高对疫苗中Pn血清型的特异性。Pn测定法利用接种PNEUMOVAX 23疫苗的受试者的免疫后血清作为标准品,来测定成人和婴儿疫苗临床试验中血清中的免疫球蛋白G浓度。该材料以Pn参考标准血清89SF为参照进行校准,并经过默克Pn ELISA吸附剂处理。对默克Pn测定法和国际Pn测定法进行了比较,结果表明两种测定形式之间具有中等程度的一致性。本文描述了默克Pn测定法的测试程序和操作特性,以及将默克Pn ELISA与国际Pn ELISA进行比较的实验结果。