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首页> 外文期刊>Journal of Clinical Microbiology >Human Cytomegalovirus Immediate-Early mRNA Detection by Nucleic Acid Sequence-Based Amplification as a New Parameter for Preemptive Therapy in Bone Marrow Transplant Recipients
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Human Cytomegalovirus Immediate-Early mRNA Detection by Nucleic Acid Sequence-Based Amplification as a New Parameter for Preemptive Therapy in Bone Marrow Transplant Recipients

机译:通过基于核酸序列的扩增人类巨细胞病毒立即早期mRNA检测作为抢先治疗骨髓移植受者的新参数。

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摘要

Human cytomegalovirus (HCMV) infection was monitored retrospectively by qualitative determination of immediate-early (IE) mRNA by nucleic acid sequence-based amplification (NASBA) in a series of 51 bone marrow transplant (BMT) recipients. The qualitative results for IE mRNA obtained by NASBA were compared with those obtained by prospective quantitation of HCMV viremia and antigenemia and retrospective quantitation of DNA in blood (DNAemia) by PCR as well as by qualitative determination of late pp67 mRNA by NASBA. On the whole, of the 39 HCMV-positive patients (all asymptomatic), HCMV was detected in 14 (35.9%) by quantitation of viremia, 15 (38.5%) by detection of pp67 mRNA by NASBA, 32 (82.1%) by quantitation of DNAemia, and 33 (84.6%) by quantitation of antigenemia, while HCMV was detected in 38 (97.4%) patients by detection of IE mRNA by NASBA. In the immunocompetent host, IE mRNA was not detected by NASBA in 100 blood donors or during reactivated infections in 30 breast-feeding mothers. Likewise, NASBA did not detect IE mRNA in 56 solid-organ transplant recipients in the first 21 days after transplantation. By using NASBA for detection of IE mRNA as the reference standard for detection of HCMV infection in blood samples, the diagnostic sensitivities were 67.7% for quantitation of DNAemia, 59.0% for quantitation of antigenemia, 18.3% for detection of pp67 mRNA by NASBA, and 16.0% for quantitation of viremia. Specificities and negative and positive predictive values were >90.0, >70.0, and >80.0%, respectively, for all four assays. The mean times to first HCMV detection after bone marrow transplantation were 37.7 ± 15.4 days for detection of IE mRNA by NASBA, 39.6 ± 15.6 days for quantitation of antigenemia, 40.9 ± 15.2 days for quantitation of DNAemia, and 43.7 ± 16.3 or 43.7 ± 17.5 days for quantitation of viremia and detection of pp67 mRNA by NASBA, respectively. On the whole, 31 BMT recipients received preemptive therapy by using confirmed antigenemia positivity as a cutoff, while 35 patients could have been treated by using NASBA positivity as a cutoff and 31 could have been treated by using quantitation of DNAemia as a cutoff. In single patients, IE mRNA was detected in every episode of active HCMV infection, mostly preceding and sometimes accompanying antigenemia and DNAemia, whereas pp67 mRNA was detected only concomitantly with the highest peaks of infection. HCMV IE mRNA detection may represent a useful parameter for initiation of preemptive therapy in BMT recipients.
机译:通过对51例骨髓移植(BMT)接受者中基于核酸序列的扩增(NASBA)进行定性测定即早(IE)mRNA来回顾性监测人类巨细胞病毒(HCMV)感染。将NASBA获得的IE mRNA的定性结果与HCMV病毒血症和抗原血症的前瞻性定量,血液中DNA的回顾性定量(DNAemia)(通过PCR)以及NASBA定性确定晚pp67 mRNA的结果进行了比较。总体而言,在39例HCMV阳性患者(全部无症状)中,通过病毒血症定量检测到HCMV的有14例(35.9%),通过NASBA检测pp67 mRNA检测的有15例(38.5%),通过定量检测的有32例(82.1%) DNA抗体的检出率为33%(84.6%),而通过NASBA检测IE mRNA的38例患者(97.4%)检出了HCMV。在具有免疫能力的宿主中,NASBA在100名献血者中或在30名母乳喂养的母亲中再次感染期间未检测到IE mRNA。同样,在移植后的前21天,NASBA在56位实体器官移植接受者中也未检测到IE mRNA。通过使用NASBA用于检测IE mRNA的检测作为检测血液样本中HCMV感染的参考标准,对DNAemia的定量诊断灵敏度为67.7%,对抗原血症的定量诊断灵敏度为59.0%,对于通过NASBA检测pp67 mRNA的诊断灵敏度为18.3%, 16.0%用于病毒血症定量。对于所有四种测定,特异性以及阴性和阳性预测值分别为> 90.0,> 70.0和> 80.0%。骨髓移植后首次进行HCMV检测的平均时间为NASBA检测IE mRNA的时间为37.7±15.4天,抗原血症的定量时间为39.6±15.6天,DNAemia的定量时间为40.9±15.2天,43.7±16.3或43.7±17.5天分别用于病毒血症定量和NASBA检测pp67 mRNA。总体上,有31名BMT接受者通过使用确定的抗原血症阳性作为临界值接受了抢先治疗,而35例患者可以通过NASBA阳性作为临界值接受治疗,而31例可以通过定量DNAemia作为临界值接受治疗。在单例患者中,在每次活动性HCMV感染的每个发作中都检测到IE mRNA,大多数是在抗原血症和DNA血症发生之前(有时是伴随),而pp67 mRNA仅在感染高峰时同时检测到。 HCMV IE mRNA检测可能代表BMT接受者开始抢先治疗的有用参数。

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