ELISA、抗原血症法和巢式PCR检测肾移植患者巨细胞病毒感染的比较

E. Moghanloo, V. Babaei, S. Rezaei, Leila Khanmirzaei, Tina Delsouz Bahri, H. Z. Gohardani, S. Teimourian
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摘要

人巨细胞病毒(HCMV)可通过输血和器官移植传播,可引起实体器官移植受者的一些并发症。本研究旨在比较ELISA、Antigenemia assay和巢式PCR检测肾移植患者巨细胞病毒感染的敏感性和特异性。本研究采集了200例肾移植患者的血液样本。用商用试剂盒提取DNA,用2对内外引物进行巢式PCR。ELISA法检测抗CMV抗体(IgM和IgG), CMV-pp65抗原血症测定(Ag)法检测CMV抗原。对各试验及各方法的敏感性和特异性进行综合评价,并采用SPSS软件对数据进行分析。200例患者中,193例(96.5%)CMV抗体阳性,特异性为100,敏感性为97.76%。巢式PCR和Ag法检测阳性120例(60%)和25例(12.5),特异性分别为94.49和78.12,敏感性分别为94.49和78.12。在疾病早期诊断的情况下,巢式PCR诊断感染比Ag检测早14年,并且始终呈阳性,而pp65 Ag检测经常观察到假阴性结果。两种方法联合检测巨细胞病毒感染的敏感性和特异性分别为96.76%和99.89%。ELISA可作为一种筛选可靠的检测受体巨细胞病毒感染的试验,特别是在无法获得PCR的情况下。ELISA与CMV- pcr相结合,为CMV感染的监测提供了更有效的方法。
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Comparison of ELISA, Antigenemia Assay and Nested PCR Monitoring Techniques for Detection of Cytomegalovirus Infection in Renal Transplantation Patients
Human cytomegalovirus (HCMV) can be transmitted through blood transfusion and organ transplantation and could be cause of some complication in solid-organ transplant recipients. Current study is aimed to compare the sensitivity and Specificity of ELISA, Antigenemia assay and nested PCR methods to detection of Cytomegalovirus infection in renal transplantation patients. In this study blood samples were collected from 200 renal transplant recipients’ patients. DNA was extracted by commercial kit and Nested PCR was done by 2 pairs of internal and external primers. Anti CMV antibodies (IgM and IgG) were detected by ELISA and CMV-pp65 antigenemia assay (Ag) was used to detect CMV antigens. The sensitivity and Specificity of each test and all the methods together were evaluated, and SPSS software was used to analysis of data. From 200 patients, 193 (96.5%) were positive for CMV antibodies with the Specificity of 100 and sensitivity of 97.76%. 120 (60%) and 25 (12.5) samples were positive by nested PCR and Ag assay with the Specificity of 94.49 and 78.12 and sensitivity of 94.49 and 78.12, respectively. In the case of early diagnosis of the disease, nested PCR diagnose the infection 14 years earlier than Ag assay and was consistently positive, whereas false negative results were frequently observed with the pp65 Ag assay. The sensitivity and specificity of the two methods combined detection for CMV infection were 96.76% and 99.89%. ELISA can be used as a screening reliable detection test for CMV infection in recipient especially when PCR is unavailable. Combination of ELISA and CMV-PCR methods, provide a more effective method to monitor CMV infection.
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