首页> 外文期刊>Journal of Clinical Microbiology >Use of quantitative competitive PCR to measure Epstein-Barr virus genome load in the peripheral blood of pediatric transplant patients with lymphoproliferative disorders.
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Use of quantitative competitive PCR to measure Epstein-Barr virus genome load in the peripheral blood of pediatric transplant patients with lymphoproliferative disorders.

机译:使用定量竞争PCR测量患有淋巴细胞增生性疾病的小儿移植患者外周血中的爱泼斯坦-巴尔病毒基因组负荷。

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摘要

A quantitative competitive PCR (QC-PCR) assay for Epstein-Barr virus (EBV) has been developed to provide accurate measurement of EBV genome load in pediatric transplant recipients at risk for developing posttransplant lymphoproliferative disorder (PTLD). The assay quantifies between 8 and 5,000 copies of the EBV genome in 10(5) lymphocytes after a 30-cycle amplification reaction. For 14 pediatric patients diagnosed with PTLD, the median EBV genome load was 4,000, and 13 of the 14 patients had values of >500 copies per 10(5) lymphocytes. Only 3 of 12 control transplant recipients not diagnosed with PTLD had detectable viral genome loads (median value, 40). This median was calculated by using the highest value obtained by PCR testing on each of these patients posttransplantation. PCR values of >500 copies per 10(5) lymphocytes appear to correlate with a diagnosis of PTLD. By a modified protocol, the EBV genome copy number in latently infected adults was estimated to be <0.1 copy per 10(5) lymphocytes.
机译:已经开发了一种针对爱泼斯坦-巴尔病毒(EBV)的定量竞争PCR(QC-PCR)分析方法,以提供对有发生移植后淋巴细胞增生性疾病(PTLD)风险的小儿移植接受者EBV基因组负荷的准确测量。经过30个循环的扩增反应后,该测定法可量化10(5)个淋巴细胞中EBV基因组的8到5,000个拷贝。对于14位诊断为PTLD的儿科患者,中位EBV基因组负载为4,000,而14位患者中的13位患者每10(5)个淋巴细胞的拷贝值大于500。在未诊断为PTLD的12名对照移植受者中,只有3名具有可检测的病毒基因组负荷(中位值为40)。该中位数是通过对每个这些患者在移植后使用PCR测试获得的最高值计算得出的。每10(5)个淋巴细胞的PCR值> 500拷贝似乎与PTLD的诊断相关。通过修改后的协议,在潜伏感染的成年人中,EBV基因组拷贝数估计每10(5)个淋巴细胞<0.1个拷贝。

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