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肾移植后巨细胞病毒病诊断中RFLP-PCR法与pp65抗原血症检测法对pp65抗原检测的比较。

Comparison between RFLP-PCR and antigenemia for pp65 antigen for diagnosis of cytomegalovirus disease after kidney transplantation.

作者信息

Schröeder R, Michelon T, Fagundes I, Bortolotto A, Petry M, Lammerhirt E, Santos L, Cantarelli V, Keitel E, Garcia V, Neumann J

机构信息

Laboratory of Transplant Immunology, Santa Casa Hospital, Porto Alegre, RS, Brazil.

出版信息

Transplant Proc. 2004 May;36(4):891-3. doi: 10.1016/j.transproceed.2004.03.059.

Abstract

Cytomegalovirus (CMV) infection is the single most frequent infectious complication in renal transplant recipients. The purpose of this study was to analyze the diagnostic efficacy of PCR-RFLP compared to antigenemia for CMV disease (CMVD) in kidney transplant recipients. From November 2001 to February 2002, 19 renal adult transplant recipients were followed with weekly measurements of CMV pp65 antigen to monitor the activity of CMV from the week 4 to 12 posttransplantation. Only 4 (21.1%) patients did not develop viremia during the first 12 posttransplantation weeks. Active infection was observed in 15 patients (78.9%): asymptomatic viremia in 6 (31.6%) and CMVD in 9 (47%). All patients who developed CMVD showed positivity in both methods during the observation period. The number of positive cells ranged from 11 to 292 cells in patients with CMVD and one to eight cells among those with asymptomatic viremia. Both methods revealed 100% sensitivity for CMVD diagnosis. The specificity was 60% for antigenemia and 70% for PCR, with positive predictive values of 60% and 75%, respectively.

摘要

巨细胞病毒(CMV)感染是肾移植受者中最常见的单一感染并发症。本研究的目的是分析与抗原血症相比,聚合酶链反应-限制性片段长度多态性(PCR-RFLP)对肾移植受者巨细胞病毒病(CMVD)的诊断效能。从2001年11月至2002年2月,对19例成年肾移植受者进行随访,每周检测CMV pp65抗原,以监测移植后第4周至12周的CMV活性。在移植后的前12周内,只有4例(21.1%)患者未发生病毒血症。15例患者(78.9%)观察到活动性感染:6例(31.6%)为无症状病毒血症,9例(47%)为CMVD。所有发生CMVD的患者在观察期内两种方法均呈阳性。CMVD患者的阳性细胞数为11至292个,无症状病毒血症患者的阳性细胞数为1至8个。两种方法对CMVD诊断的敏感性均为100%。抗原血症的特异性为60%,PCR的特异性为70%,阳性预测值分别为60%和75%。

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