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Development of a New Cytomegalovirus (CMV) Immunoglobulin M (IgM) Immunoblot for Detection of CMV-Specific IgM

机译:新型巨细胞病毒(CMV)免疫球蛋白M(IgM)免疫印迹技术的开发用于检测CMV特异性IgM

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摘要

We developed a new cytomegalovirus (CMV) immunoglobulin M (IgM) immunoblot to detect CMV-specific IgM in human sera. The new test contains four viral proteins (vp150, vp82, vp65, and vp28) purified from viral particles and four recombinant proteins (rp150, rp130, rp52, and rp38) purified from Escherichia coli. These antigens were individually loaded onto nitrocellulose strips, and the strips were then used to detect CMV-specific IgM by using a μ-specific conjugate. The new assay was evaluated in parallel with one or two IgM enzyme-linked immunosorbent assays (ELISAs) to test 592 serum samples from different groups of latently or acutely infected individuals. The sensitivity of the new assay with respect to the consensus of two ELISAs was 100%, the specificity was 98.6%, the positive predictive value was 96.9%, and the negative predictive value was 100%. We also evaluated the new test by testing sera from pregnant women and transplant recipients with a known clinical history. Our results suggest that the new test combines high sensitivity with high specificity, characteristics that are mutually exclusive with the other commercially available tests. Furthermore, a statistically significant correlation was observed between the number of IgM-reactive bands and the elevated risk of transmission from CMV-infected pregnant women to their offspring.
机译:我们开发了一种新的巨细胞病毒(CMV)免疫球蛋白M(IgM)免疫印迹,以检测人血清中CMV特异性IgM。新测试包含从病毒颗粒中纯化得到的四种病毒蛋白(vp150,vp82,vp65和vp28)和从大肠杆菌中纯化出的四种重组蛋白(rp150,rp130,rp52和rp38)。将这些抗原分别上样到硝酸纤维素条上,然后将这些条用于通过使用μ特异性结合物检测CMV特异性IgM。与一种或两种IgM酶联免疫吸附测定(ELISA)并行评估新测定,以测试来自潜伏性或急性感染个体不同组的592个血清样品。相对于两次ELISA的一致性,新方法的敏感性为100%,特异性为98.6%,阳性预测值为96.9%,阴性预测值为100%。我们还通过检测孕妇和具有已知临床病史的移植患者的血清来评估新测试。我们的结果表明,新测试结合了高灵敏度和高特异性,这些特性与其他市售测试互斥。此外,在IgM反应性条带数量与从CMV感染的孕妇到其后代的传播风险升高之间存在统计学上的显着相关性。

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