Marins Ed G, Bodinaidu Keerthi, Lin Matthew, Deforest Alison
Roche Molecular Systems, 4300 Hacienda Dr, Pleasanton, CA, 94588, United States.
Roche Molecular Systems, 4300 Hacienda Dr, Pleasanton, CA, 94588, United States.
J Virol Methods. 2017 Sep;247:77-80. doi: 10.1016/j.jviromet.2017.05.016. Epub 2017 May 30.
This study evaluated the use of dried blood spot (DBS) for HCV viral load quantification using the COBAS AmpliPrep/COBAS Taqman HCV Quantitative Test v2.0 (CAP/CTM HCV v2), and compared two different procedures for preparation of DBS samples with a Specimen Pre-Extraction (SPEX) reagent (either heated [SPEX with SH] for 10min at 56°C on a thermomixer, or incubated for 1h at room temperature [SPEX at RT]) against the standard plasma input. Whole blood specimens from 48 patients with chronic HCV infection and Whatman 903 Protein Saver Cards were used to prepare 35μL DBS. An aliquot of plasma was spun and frozen from each draw. Mean DBS viral load results were compared to the corresponding results from plasma. Correlation between DBS to plasma was linear for both SPEX with SH (R=0.96) and SPEX at RT (R=0.97) procedures, with a constant negative offset of approximately 2.0logIU/mL between whole blood DBS without any adjustments and plasma results. After volume corrections, the mean offset to plasma decreased to -0.39 and -0.36 for the two procedures, respectively. The study demonstrated the use of DBS for HCV viral load correlates well with plasma with a constant offset.
本研究评估了使用干血斑(DBS)通过COBAS AmpliPrep/COBAS Taqman HCV定量检测v2.0(CAP/CTM HCV v2)对丙型肝炎病毒(HCV)载量进行定量,并将使用标本预提取(SPEX)试剂制备DBS样本的两种不同程序(在热混合器上于56°C加热[带SH的SPEX]10分钟,或在室温下孵育1小时[室温下的SPEX])与标准血浆输入进行比较。使用48例慢性HCV感染患者的全血标本和Whatman 903蛋白保存卡制备35μL DBS。每次采血后将一份血浆离心并冷冻。将DBS病毒载量的平均结果与血浆的相应结果进行比较。对于带SH的SPEX(R=0.96)和室温下的SPEX(R=0.97)程序,DBS与血浆之间的相关性均为线性,未经任何调整的全血DBS与血浆结果之间存在约2.0logIU/mL的恒定负偏移。经过体积校正后,两种程序与血浆的平均偏移分别降至-0.39和-0.36。该研究表明,使用DBS检测HCV病毒载量与血浆具有良好的相关性,且存在恒定偏移。