Portet Sulla Vincent, Rafek Rana, Bertin-Jung Isabelle, Siest Jean-Pascal, Bouthry Elise, Rogier Olivier, Jadoui Abir, Vauloup-Fellous Christelle, Perillaud-Dubois Claire
WHO Rubella National Reference Laboratory, Division of Virology, Department of Biology Genetics, Paul Brousse Hospital, Paris Saclay University Hospital, APHP, Villejuif, France.
Center for Immunology of Viral, Auto-immune, Hematological and Bacterial diseases (IMVA-HB/IDMIT), Paris Saclay University, INSERM U1184, CEA, Fontenay-aux-Roses, France.
Microbiol Spectr. 2025 Aug 5;13(8):e0045525. doi: 10.1128/spectrum.00455-25. Epub 2025 Jun 17.
Diagnosis of cytomegalovirus (CMV) primary infection (PI) during pregnancy relies on serology (CMV-IgG, IgM, and IgG avidity). However, as for toxoplasmosis, subsequent serology testing 3-5 weeks later is often performed to confirm the diagnosis. In this study, we aimed to show that testing CMV-IgG with different assays may lead to misinterpretation of CMV-IgG kinetics and to determine the sensitivity and specificity of CMV-IgG stability and significant increase to exclude or confirm recent CMV PI. We conducted a retrospective study on (i) a CMV-IgG external quality control program (2015-2022) and (ii) on CMV serology results obtained in our virology laboratory (2013-2023) in pregnant women with positive CMV-IgM and a subsequent serum sample collected 3-5 weeks later. Analysis of 21 CMV-IgG external quality control serum samples highlighted significant differences in CMV-IgG values, with variations up to a factor of 185 between different immunoassays for the same positive sample. In 434 pregnant women, the sensitivity of a significant CMV-IgG increase to predict recent PI was 32.9% (95% CI = 26.5-39.2), while CMV-IgG stability specificity to exclude PI <3 months was 32.9% (95% CI = 26.5-39.2). Our observations highlight the discrepancies in CMV-IgG values with different assays and the major importance of CMV-IgG avidity in the diagnosis of recent CMV PI in case of positive CMV-IgM. We also demonstrate that retesting IgG on a sample collected 3-5 weeks later is not helpful and can be confusing.IMPORTANCEThis article is the first to address cytomegalovirus (CMV)-IgG kinetics and their reliability in the serological diagnosis of CMV. In our experience, many clinical virologists and laboratory practitioners still rely on kinetics for diagnosis. However, our study clearly demonstrates that this approach is misleading and that avidity testing should always be performed. Additionally, we conducted a robust study highlighting discrepancies between CMV serology techniques, emphasizing the importance for practitioners, particularly gynecologists, to avoid monitoring serology results using different testing methods.
孕期巨细胞病毒(CMV)原发性感染(PI)的诊断依赖于血清学检测(CMV-IgG、IgM和IgG亲和力)。然而,与弓形虫病一样,通常会在3至5周后进行后续血清学检测以确诊。在本研究中,我们旨在表明,使用不同检测方法检测CMV-IgG可能会导致对CMV-IgG动力学的误解,并确定CMV-IgG稳定性及显著升高的敏感性和特异性,以排除或确诊近期的CMV PI。我们对(i)一项CMV-IgG外部质量控制计划(2015 - 2022年)以及(ii)我们病毒学实验室(2013 - 2023年)获得的CMV血清学结果进行了回顾性研究,这些结果来自CMV-IgM呈阳性且在3至5周后采集了后续血清样本的孕妇。对21份CMV-IgG外部质量控制血清样本的分析突出了CMV-IgG值的显著差异,对于同一阳性样本,不同免疫检测方法之间的差异高达185倍。在434名孕妇中,CMV-IgG显著升高以预测近期PI的敏感性为32.9%(95%置信区间 = 26.5 - 39.2),而CMV-IgG稳定性用于排除3个月内PI的特异性为32.9%(95%置信区间 = 26.5 - 39.2)。我们的观察结果突出了不同检测方法下CMV-IgG值的差异,以及在CMV-IgM呈阳性时CMV-IgG亲和力在诊断近期CMV PI中的重要性。我们还证明,对3至5周后采集的样本重新检测IgG并无帮助且可能会造成混淆。
重要性
本文首次探讨了巨细胞病毒(CMV)-IgG动力学及其在CMV血清学诊断中的可靠性。根据我们的经验,许多临床病毒学家和实验室工作人员仍依赖动力学进行诊断。然而,我们的研究清楚地表明这种方法具有误导性,应始终进行亲和力检测。此外,我们进行了一项有力的研究,突出了CMV血清学技术之间的差异,强调了从业者,尤其是妇科医生,避免使用不同检测方法监测血清学结果的重要性。