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骨髓移植受者中人巨细胞病毒DNA的定量分析。

Quantitation of human cytomegalovirus DNA in bone marrow transplant recipients.

作者信息

Gerna G, Furione M, Baldanti F, Percivalle E, Comoli P, Locatelli F

机构信息

Viral Diagnostic Service, University of Pavia, I.R.C.C.S. Policlinico S. Matteo, Italy.

出版信息

Br J Haematol. 1995 Nov;91(3):674-83. doi: 10.1111/j.1365-2141.1995.tb05368.x.

Abstract

HCMV DNA was retrospectively quantitated in the early post-transplant period in 36 paediatric bone marrow transplant (BMT) recipients prospectively monitored for human cytomegalovirus (HCMV) infection on the basis of antigenaemia and viraemia assays. Viral DNA was quantitated in peripheral blood leucocytes (PBL) by PCR using an internal control of amplification and a series of external standards. Densitometric analysis of hybridization results obtained on PCR products enabled construction of a standard curve from which DNA amounts of clinical samples, expressed in terms of genome equivalents (GE), were interpolated. Of the 36 BMT recipients, three had clinically symptomatic HCMV infection with mean peak levels of viral DNA > 5000 GE (antigenaemia and viraemia mean peak levels were 873 and 35, respectively), whereas 19 with HCMV reactivation were asymptomatic (five of them had abortive HCMV infection) showing mean peak DNA levels of 131 GE (and of 6.8 and 1.3 for antigenaemia and viraemia, respectively) (P < or = 0.01). Single or multiple courses of pre-emptive therapy with ganciclovir or foscarnet were given to 14/19 asymptomatic children in whom antigenaemia levels were > 2 or lower yet persisting. Overall, in the 14 asymptomatic treated patients the mean antigenaemia level was 9.3 (range 1-22), and the mean DNA level was 184.6 (range 20-710) GE. Antiviral drugs were also administered to the three symptomatic patients who, due to late diagnosis of HCMV infection, escaped preemptive therapy. Antiviral treatment caused marked decrease or disappearance of viral DNA, antigenaemia and viraemia in both symptomatic and asymptomatic patients. In conclusion, our study suggests that: (i) starting therapy in the presence of a mean antigenaemia level of 9.3 (range 1-22) corresponding to a mean DNA level of 184.6 (range 20-710) GE avoided occurrence of any major HCMV-related clinical complication; (ii) clinical symptoms were associated with antigenaemia levels > 100 and DNA levels > 1000 GE; (iii) the effect of antiviral treatment could be more carefully monitored by quantitation of viral DNA.

摘要

对36名接受儿科骨髓移植(BMT)的患者在移植后早期进行了人巨细胞病毒(HCMV)DNA的回顾性定量分析,这些患者基于抗原血症和病毒血症检测对HCMV感染进行前瞻性监测。通过使用扩增内对照和一系列外标,采用聚合酶链反应(PCR)对外周血白细胞(PBL)中的病毒DNA进行定量。对PCR产物杂交结果进行光密度分析,从而构建标准曲线,据此推算出以基因组当量(GE)表示的临床样本的DNA量。36名BMT受者中,3例出现临床症状性HCMV感染,病毒DNA平均峰值水平>5000 GE(抗原血症和病毒血症平均峰值水平分别为873和35),而19例HCMV再激活者无症状(其中5例为顿挫型HCMV感染),DNA平均峰值水平为131 GE(抗原血症和病毒血症的平均峰值水平分别为6.8和1.3)(P≤0.01)。对19例无症状儿童中抗原血症水平>2或较低但持续存在的14例给予单疗程或多疗程更昔洛韦或膦甲酸钠抢先治疗。总体而言,14例接受治疗的无症状患者的平均抗原血症水平为9.3(范围1 - 22),平均DNA水平为184.6(范围20 - 710)GE。对3例有症状的患者也给予了抗病毒药物治疗,这3例患者因HCMV感染诊断较晚而未接受抢先治疗。抗病毒治疗使有症状和无症状患者的病毒DNA、抗原血症和病毒血症均显著下降或消失。总之,我们的研究表明:(i)在平均抗原血症水平为9.3(范围1 - 22)、对应平均DNA水平为184.6(范围20 - 710)GE时开始治疗,可避免发生任何与HCMV相关的重大临床并发症;(ii)临床症状与抗原血症水平>100和DNA水平>1000 GE相关;(iii)通过病毒DNA定量可更仔细地监测抗病毒治疗的效果。

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