Sowers Sun B, Rota Jennifer S, Hickman Carole J, Mercader Sara, Redd Susan, McNall Rebecca J, Williams Nobia, McGrew Marcia, Walls M Laura, Rota Paul A, Bellini William J
National Center for Immunization and Respiratory Diseases, Division of Viral Diseases, Centers for Disease Control and Prevention (CDC), Atlanta, Georgia, USA
National Center for Immunization and Respiratory Diseases, Division of Viral Diseases, Centers for Disease Control and Prevention (CDC), Atlanta, Georgia, USA.
Clin Vaccine Immunol. 2016 Aug 5;23(8):707-16. doi: 10.1128/CVI.00268-16. Print 2016 Aug.
In the United States, approximately 9% of the measles cases reported from 2012 to 2014 occurred in vaccinated individuals. Laboratory confirmation of measles in vaccinated individuals is challenging since IgM assays can give inconclusive results. Although a positive reverse transcription (RT)-PCR assay result from an appropriately timed specimen can provide confirmation, negative results may not rule out a highly suspicious case. Detection of high-avidity measles IgG in serum samples provides laboratory evidence of a past immunologic response to measles from natural infection or immunization. High concentrations of measles neutralizing antibody have been observed by plaque reduction neutralization (PRN) assays among confirmed measles cases with high-avidity IgG, referred to here as reinfection cases (RICs). In this study, we evaluated the utility of measuring levels of measles neutralizing antibody to distinguish RICs from noncases by receiver operating characteristic curve analysis. Single and paired serum samples with high-avidity measles IgG from suspected measles cases submitted to the CDC for routine surveillance were used for the analysis. The RICs were confirmed by a 4-fold rise in PRN titer or by RT-quantitative PCR (RT-qPCR) assay, while the noncases were negative by both assays. Discrimination accuracy was high with serum samples collected ≥3 days after rash onset (area under the curve, 0.953; 95% confidence interval [CI], 0.854 to 0.993). Measles neutralizing antibody concentrations of ≥40,000 mIU/ml identified RICs with 90% sensitivity (95% CI, 74 to 98%) and 100% specificity (95% CI, 82 to 100%). Therefore, when serological or RT-qPCR results are unavailable or inconclusive, suspected measles cases with high-avidity measles IgG can be confirmed as RICs by measles neutralizing antibody concentrations of ≥40,000 mIU/ml.
在美国,2012年至2014年报告的麻疹病例中约9%发生在已接种疫苗的个体中。对已接种疫苗个体进行麻疹的实验室确诊具有挑战性,因为IgM检测结果可能不明确。虽然适时采集的样本经逆转录(RT)-PCR检测呈阳性结果可提供确诊依据,但阴性结果可能无法排除高度可疑病例。血清样本中高亲和力麻疹IgG的检测为既往自然感染或免疫接种后对麻疹产生的免疫反应提供了实验室证据。通过蚀斑减少中和(PRN)试验在具有高亲和力IgG的确诊麻疹病例(在此称为再感染病例,RICs)中观察到高浓度的麻疹中和抗体。在本研究中,我们通过受试者操作特征曲线分析评估了检测麻疹中和抗体水平以区分再感染病例与非病例的效用。提交给美国疾病控制与预防中心(CDC)进行常规监测的疑似麻疹病例的单份和配对高亲和力麻疹IgG血清样本用于分析。再感染病例通过PRN滴度升高4倍或RT定量PCR(RT-qPCR)检测确诊,而非病例两项检测均为阴性。皮疹出现后≥3天采集的血清样本判别准确率较高(曲线下面积为0.953;95%置信区间[CI]为0.854至0.993)。麻疹中和抗体浓度≥40,000 mIU/ml识别再感染病例的灵敏度为90%(95% CI为74%至98%),特异性为100%(95% CI为82%至100%)。因此,当血清学检测或RT-qPCR结果不可用或不明确时,麻疹中和抗体浓度≥40,000 mIU/ml的疑似麻疹病例且具有高亲和力麻疹IgG可确诊为再感染病例。