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首页> 外文期刊>Brazilian Journal of Medical and Biological Research >Monitoring human cytomegalovirus viral load in peripheral blood leukocytes of renal transplant recipients by a simple limiting dilution-PCR assay
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Monitoring human cytomegalovirus viral load in peripheral blood leukocytes of renal transplant recipients by a simple limiting dilution-PCR assay

机译:通过简单的有限稀释PCR法监测肾移植受者外周血白细胞中人巨细胞病毒的病毒载量

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To assess the clinical relevance of a semi-quantitative measurement of human cytomegalovirus (HCMV) DNA in renal transplant recipients within the typical clinical context of a developing country where virtually 100% of both receptors and donors are seropositive for this virus, we have undertaken HCMV DNA quantification using a simple, semi-quantitative, limiting dilution polymerase chain reaction (PCR). We evaluated this assay prospectively in 52 renal transplant patients from whom a total of 495 serial blood samples were collected. The samples scored HCMV positive by qualitative PCR had the levels of HCMV DNA determined by end-point dilution-PCR. All patients were HCMV DNA positive during the monitoring period and a diagnosis of symptomatic infection was made for 4 of 52 patients. In symptomatic patients the geometric mean of the highest level of HCMV DNAemia was 152,000 copies per 106 leukocytes, while for the asymptomatic group this value was 12,050. Symptomatic patients showed high, protracted HCMV DNA levels, whereas asymptomatic patients demonstrated intermittent low or moderate levels. Using a cut-off value of 100,000 copies per 106 leukocytes, the limiting dilution assay had sensitivity of 100%, specificity of 92%, a positive predictive value of 43% and a negative predictive value of 100% for HCMV disease. In this patient group, there was universal HCMV infection but relatively infrequent symptomatic HCMV disease. The two patient groups were readily distinguished by monitoring with the limiting dilution assay, an extremely simple technology immediately applicable in any clinical laboratory with PCR capability.
机译:为了评估在发展中国家典型临床情况下肾脏移植受者中人类巨细胞病毒(HCMV)DNA的半定量测量的临床相关性,在该国家中,实际上受体和供体两者均对该病毒呈血清阳性,我们进行了HCMV使用简单,半定量,有限稀释的聚合酶链反应(PCR)进行DNA定量。我们对52名肾移植患者的前瞻性评估结果进行了评估,共收集了495份系列血样。通过定性PCR评分为HCMV阳性的样品具有通过终点稀释PCR测得的HCMV DNA水平。在监测期间,所有患者的HCMV DNA均为阳性,并诊断出52例患者中有4例有症状感染。在有症状的患者中,HCMV DNAemia最高水平的几何平均值为每106个白细胞152,000份,而无症状组的该平均值为12,050。有症状的患者表现出高水平,长期的HCMV DNA水平,而无症状的患者表现出间歇性低或中等水平。使用每106个白细胞100,000个拷贝的临界值,有限稀释测定法对HCMV疾病的敏感性为100%,特异性为92%,阳性预测值为43%,阴性预测值为100%。在该患者组中,存在普遍的HCMV感染,但症状性HCMV疾病相对较少。通过用有限稀释测定法进行监测很容易地区分这两个患者组,这是一种极其简单的技术,可立即应用于具有PCR功能的任何临床实验室。

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