Department of Medical Microbiology, University Medical Center Utrecht, Heidelberglaan 100, 3584CX, the Netherlands.
Department of Medical Microbiology, University Medical Center Utrecht, Heidelberglaan 100, 3584CX, the Netherlands.
J Clin Virol. 2024 Oct;174:105722. doi: 10.1016/j.jcv.2024.105722. Epub 2024 Aug 24.
Adenovirus infections constitute an important cause of morbidity and mortality after hematopoietic stem cell transplantation. Detection and monitoring of adenovirus in EDTA-plasma by real-time quantitative PCR is a sensitive tool for identification and management of patients at risk of a potentially fatal infection.
The aim of this study was to evaluate the analytical and clinical performance of the quantitative Adenovirus ELITe MGB® Kit (ELITechGroup S.p.A.) using the ELITe BeGenius® (ELITechGroup S.p.A.) system and compare the assay to a laboratory-developed quantitative real-time PCR assay.
Analytical sensitivity of the Adenovirus ELITe MGB® Kit was determined by testing serial dilutions of the WHO standard. Detection of adenovirus serotypes was assessed using a panel of 51 serotypes. Clinical sensitivity and specificity were determined by comparing the Adenovirus ELITe MGB® Kit results with the laboratory-developed assay results of 155 retrospective and prospective EDTA-plasma samples from transplant recipients.
The analytical sensitivity of the Adenovirus ELITe MGB® Kit was at least 54 (1.7 Log) IU/mL and the quantitative results showed a high correlation with the WHO standard (R = 0.9978; Pearson) within the range of 1.7 to 6.6 Log IU/mL. All 51 adenovirus serotypes were detected. The clinical specificity and sensitivity for EDTA plasma of the Adenovirus ELITe MGB® Kit were 97.4 % and 99.1 % respectively.
The Adenovirus ELITe MGB® Kit performed on the ELITe BeGenius® system is a highly sensitive and specific assay for the detection of adenovirus in EDTA-plasma from transplantation patients.
腺病毒感染是造血干细胞移植后发病率和死亡率的重要原因。通过实时定量 PCR 检测 EDTA 血浆中的腺病毒是识别和管理有潜在致命感染风险患者的敏感工具。
本研究旨在评估使用 ELITe BeGenius®(ELITechGroup S.p.A.)系统的定量腺病毒 ELITe MGB®试剂盒(ELITechGroup S.p.A.)的分析和临床性能,并将该测定方法与实验室开发的定量实时 PCR 测定方法进行比较。
通过测试世界卫生组织标准的系列稀释液来确定腺病毒 ELITe MGB®试剂盒的分析灵敏度。使用 51 种血清型的面板评估腺病毒血清型的检测。通过将腺病毒 ELITe MGB®试剂盒的结果与来自移植受者的 155 份回顾性和前瞻性 EDTA 血浆样本的实验室开发的测定结果进行比较,确定临床敏感性和特异性。
腺病毒 ELITe MGB®试剂盒的分析灵敏度至少为 54(1.7 Log)IU/mL,定量结果在 1.7 至 6.6 Log IU/mL 的范围内与世界卫生组织标准高度相关(R = 0.9978;Pearson)。所有 51 种腺病毒血清型均被检测到。用于 EDTA 血浆的腺病毒 ELITe MGB®试剂盒的临床特异性和敏感性分别为 97.4%和 99.1%。
ELITe BeGenius®系统上的腺病毒 ELITe MGB®试剂盒是一种高度敏感和特异的检测方法,可用于检测移植患者 EDTA 血浆中的腺病毒。