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Pitfalls in the Serological Diagnosis of Primary Human Cytomegalovirus Infection in Pregnancy Due to Different Kinetics of IgM Clearance and IgG Avidity Index Maturation

机译:由于IGM间隙和IgG Andity指数成熟的不同动力学妊娠期原发性人巨细胞病毒感染血清诊断缺陷

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摘要

Primary infection occurs when seronegative women are infected by human cytomegalovirus (HCMV). Diagnosis of primary infection is based on the following: antibody seroconversion, presence of IgM and low IgG avidity index (AI), and presence of DNAemia. The kinetics of HCMV-specific IgM antibody and maturation of AI might be very rapid or long-lasting during primary infection, which makes serological diagnosis insidious. The aims of this study were as follows: (i) to report atypical kinetics of HCMV-specific IgM antibody and AI early after onset of primary HCMV infection in a population of pregnant women, and (ii) to assess the frequency of such results. Altogether, 1309 sequential serum samples collected from 465 pregnant women with primary HCMV infection were included in the study. As a general rule, using the LIAISON®CMVIgMII and LIAISON®CMVIgGAvidityII assays, virus-specific IgM antibody levels decreased, while IgG AI increased over time during the first three months after infection onset. However, early clearance of IgM antibody and/or early IgG AI maturation occurred in 46/426 (10.7%) women. In more details, 20/426 (4.7%) and 26/418 (6.2%) women had undetectable IgM antibody or high IgG AI, respectively, when tested within 1–3 months after well-defined infection onset. Twenty sera from as many women with high IgG AI by the LIAISON assay were further tested for IgG AI by VIDAS®CMVIgGAvidityII and Mikrogen recomLineCMVIgG Avidity assays. Comparable results were obtained with VIDAS, whereas 14/20 sera gave low AI with the Mikrogen assay. In conclusion, about 11% of pregnant women undergoing a primary HCMV infection showed misleading serological results. Additional and appropriate testing might help in reducing the risk of missing HCMV primary infection in pregnancy. Furthermore, preconceptional testing should be strongly recommended.
机译:当患有人巨细胞病毒(HCMV)感染时,发生原发性感染。诊断原发性感染是基于以下内容:抗体血清转化,IgM的存在和低IgG耐酸性指数(AI)和Dnaemia的存在。在原发性感染期间,HCMV特异性IgM抗体和AI成熟的动力学可能是非常快速或持久的,这使血清学诊断阴险。本研究的目的如下:(i)在孕妇群中发起原发性HCMV感染后早期报告HCMV特异性IgM抗体和AI的非典型动力学,以及(ii)评估此类结果的频率。在研究中,从465名孕妇收集的1309个序贯血清样本均包含在研究中。作为一般规则,使用Liaison®Cmvigmii和Liaison®Cmviggavi催化测定,病毒特异性IgM抗体水平降低,而IgG AI在感染发生后的前三个月内随着时间的推移而增加。然而,IgM抗体和/或早期IgG AI成熟的早期间隙发生在46/426(10.7%)妇女中发生。更详细的详细信息,20/426(4.7%)和26/418(6.2%)妇女分别具有未检测到的IgM抗体或高IgG AI,当在定义明确的感染发生后1-3个月内测试。由vidas®Cmviggavigiyii和Mikrogen RecomlinecMvigg Andify测定的IgG AI进一步测试了来自与联络测定的许多具有高IgG AI的女性的二十六种血清。用VIDA获得可比较的结果,而14/20血清具有MikOr原测定的低a。总之,大约11%的孕妇正在进行一次HCMV感染,显示出误导性血清学结果。其他和适当的测试可能有助于降低怀孕缺失HCMV原发性感染的风险。此外,应该强烈建议先印度测试。

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