首页> 外文期刊>Journal of clinical virology: The official publication of the Pan American Society for Clinical Virology >Comparison of the Murex Hybrid Capture CMV DNA (v2.0) assay and the pp65 CMV antigenemia test for the detection and quantitation of CMV in blood samples from immunocompromised patients.
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Comparison of the Murex Hybrid Capture CMV DNA (v2.0) assay and the pp65 CMV antigenemia test for the detection and quantitation of CMV in blood samples from immunocompromised patients.

机译:Murex Hybrid Capture CMV DNA(v2.0)分析法和pp65 CMV抗原血症测试用于检测和定量免疫受损患者血样中CMV的比较。

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BACKGROUND: Presently the semiquantitative pp65 cytomegalovirus (CMV) antigenemia test on white blood cells is often used for monitoring transplant patients for the appearance of active CMV infections. However, the need for immediate processing of the specimens and the lack of interlaboratory standardization of the test may sometimes be a disadvantage. OBJECTIVE: The aim of this study was to investigate the value of the recently developed second version of the Murex Hybrid Capture (MHC) CMV-DNA assay (v 2.0) in comparison with the CMV-pp65 test. The MHC CMV-DNA assay is a quantitative solution hybridization antibody capture assay, using alkaline phosphatase conjugated antibodies and a chemiluminescent substrate. STUDY DESIGN: 248 EDTA blood samples from 33 renal transplant patients and 32 samples from 22 other immunocompromised patients were tested by both the MHC CMV-DNA assay and the CMV-pp65 test. RESULTS: The qualitative ( + or -) results of both tests showed an overall concordance of 81.4%. Calculations on the basis of discordancy analyses showed that the sensitivity, the specificity, and the positive and negative predictive values were 87.7, 98.3, 98.6, 85.2% for the MHC CMV-DNA assay and 76.6, 100, 100, 75.5% for the CMV-pp65 test. Comparison of the quantitative results of both tests systems showed a correlation coefficient of 0.837. In addition, retesting of 50 samples with the MHC-CMV-DNA assay showed an excellent reproducibility with a correlation coefficient of 0.992. All patients which were tested regularly (at least five samples) became either positive with both tests or with none of them. Neither test system detected CMV significantly earlier than the other one. Both tests became strongly positive in all transplant patients with symptomatic CMV infections, and both tests showed a rapid decline of CMV during subsequent antiviral treatment. CONCLUSION: The quantitative Murex Hybrid Capture CMV-DNA assay (v 2.0) may become a valuable additional tool in CMV diagnosis. Further studies will be needed to support this preliminary judgement.
机译:背景:目前,对白细胞进行的半定量pp65巨细胞病毒(CMV)抗原血症检测通常用于监测移植患者的活跃CMV感染情况。但是,有时需要立即处理标本并且缺乏实验室间的标准化测试可能是不利的。目的:本研究的目的是与CMV-pp65测试相比,研究最近开发的第二版Murex Hybrid Capture(MHC)CMV-DNA测定法(v 2.0)的价值。 MHC CMV-DNA分析是一种定量溶液杂交抗体捕获分析,使用碱性磷酸酶偶联的抗体和化学发光底物。研究设计:通过MHC CMV-DNA检测和CMV-pp65检测对来自33位肾移植患者的248 EDTA血液样本和来自其他22位免疫受损患者的32样本进行了检测。结果:两种测试的定性(+或-)结果显示总体一致性为81.4%。根据不一致分析进行的计算表明,MHC CMV-DNA测定的敏感性,特异性以及阳性和阴性预测值分别为87.7%,98.3、98.6、85.2%,CMV分别为76.6、100、100、75.5% -pp65测试。两种测试系统的定量结果比较表明相关系数为0.837。此外,用MHC-CMV-DNA测定法对50个样品进行重新测试显示出极好的可重复性,相关系数为0.992。定期接受检查的所有患者(至少五个样本)在两项检查中均呈阳性,或全无。两种测试系统均未比另一种系统早发现CMV。两种测试在所有有症状CMV感染的移植患者中均呈强阳性,并且两种测试均表明在随后的抗病毒治疗期间CMV迅速下降。结论:定量的Murex Hybrid Capture CMV-DNA测定(v 2.0)可能成为CMV诊断中有价值的附加工具。需要进一步的研究来支持这一初步判断。

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