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使用实时定量聚合酶链反应评估白细胞去除滤器对血液成分中人类巨细胞病毒的去除效果。

Assessment of removal of human cytomegalovirus from blood components by leukocyte depletion filters using real-time quantitative PCR.

作者信息

Visconti Micaela Rios, Pennington Joanne, Garner Stephen F, Allain Jean-Pierre, Williamson Lorna M

机构信息

Division of Transfusion Medicine, National Blood Service, Long Rd, Cambridge CB2 2PT, England.

出版信息

Blood. 2004 Feb 1;103(3):1137-9. doi: 10.1182/blood-2003-03-0762. Epub 2003 Oct 2.

Abstract

To assess removal of cytomegalovirus (CMV) by leukocyte depletion (LD) filters, we developed a spiking model of latent virus using peripheral blood mononuclear cells (PBMCs) infected by coculture with CMV-infected human fibroblasts. Infected PBMCs were purified by dual magnetic column selection and then spiked into whole blood units or buffy coat pools prior to LD by filtration. CMV load and fibroblast contamination were assessed using quantitative CMV DNA real-time PCR and quantitative reverse transcriptase-polymerase chain reaction (RT-PCR) of mRNA encoding the fibroblast-specific splice variant of prolyl-4-hydroxylase, respectively. After correcting for fibroblast-associated CMV, the mean CMV load was reduced in whole blood by LD from 7.42 x 10(2) to 1.13 copies per microliter (2.81(10)log reduction) and from 3.8 x 10(2) to 4.77 copies per microliter (1.9(10)log reduction) in platelets. These results suggest that LD by filtration reduces viral burden but does not completely remove CMV from blood components.

摘要

为评估白细胞滤除(LD)过滤器对巨细胞病毒(CMV)的去除效果,我们利用与CMV感染的人成纤维细胞共培养感染的外周血单个核细胞(PBMC)建立了一种潜伏病毒加标模型。通过双磁柱筛选纯化感染的PBMC,然后在过滤进行LD之前将其加入全血单位或 Buffy 层混合液中。分别使用定量CMV DNA实时PCR和编码脯氨酰-4-羟化酶成纤维细胞特异性剪接变体的mRNA的定量逆转录聚合酶链反应(RT-PCR)评估CMV载量和成纤维细胞污染情况。在校正与成纤维细胞相关的CMV后,全血中经LD处理后CMV平均载量从每微升7.42×10²拷贝降至1.13拷贝(2.81(10)对数减少),血小板中从每微升3.8×10²拷贝降至4.77拷贝(1.9(10)对数减少)。这些结果表明,过滤进行LD可降低病毒载量,但不能完全从血液成分中去除CMV。

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