评估新型单参数容积式流式细胞仪(CyFlow(green))在感染人类免疫缺陷病毒 1 型的泰国患者中的 CD4+ T 淋巴细胞绝对计数。

Kovit Pattanapanyasat, Surada Lerdwana, Egarit Noulsri, Thanyanan Chaowanachan, Punneeporn Wasinrapee, Natthaga Sakulploy, Vallerut Pobkeeree, Orapin Suksripanich, Sombat Thanprasertsuk, Thomas J Spira, Jordan W Tappero, William C Levine
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引用次数: 0

摘要

使用标准的双平台流式细胞计数法测定 CD4(+) T 淋巴细胞计数,需要同时使用流式细胞仪(FCM)和血液分析仪,这不可避免地会导致变异性增加。最近,能直接提供 CD4(+) T 淋巴细胞计数以提高检测精度和准确性的新型单平台(SP)流式细胞仪的开发引起了人们的关注。本研究评估了其中一种系统 CyFlow(green)(Partec),它是一种单参数 SP 容积式 FCM。CyFlow(green)的性能与两种基于SP微珠的参考标准技术进行了比较,这两种技术分别是带有FACScan FCM的三色TruCOUNT管和双色FACSCount系统(Becton Dickinson Biosciences)。测定了 200 份人类免疫缺陷病毒 1 型血清阳性血液标本中 CD4(+) 和 CD8(+) T 淋巴细胞的绝对数量。对相关性和一致性进行了统计分析。用 CyFlow(green)获得的 CD4 绝对计数与用基于珠子的三色 TruCOUNT 系统获得的 CD4 绝对计数相比,显示出很高的相关性(R(2)=0.96;平均偏差,-69.1 个细胞/微升;95% 置信区间 [CI],-225.7 至+87.5 个细胞/微升)和 FACSCount 系统(R(2)=0.97;平均偏差,-40.0 个细胞/微升;95% 置信区间,-165.1 至+85.1 个细胞/微升)。两种基于微珠的系统获得的 CD4(+) T 淋巴细胞计数的相关性很高(R(2)=0.98)。有趣的是,当 CD4(+) T 淋巴细胞计数为每微升 21.8 个细胞时,CyFlow(green) 系统得到的 CD4(+) T 淋巴细胞计数比 TruCOUNT 和 FACSCount 系统得到的分别低 21.8 和 7.2 个细胞/微升。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of a new single-parameter volumetric flow cytometer (CyFlow(green)) for enumeration of absolute CD4+ T lymphocytes in human immunodeficiency virus type 1-infected Thai patients.

Use of the standard dual-platform flow cytometric method for determination of CD4(+) T-lymphocyte counts, which needs both a flow cytometer (FCM) and hematological analyzer, would inevitably lead to increased variability. The development of new single-platform (SP) FCMs that provide direct CD4(+) T-lymphocyte counts for improved assay precision and accuracy have recently attracted attention. This study evaluated one of those systems, CyFlow(green) (Partec), a single-parameter SP volumetric FCM. The performance of CyFlow(green) was compared with those of two reference standard SP microbead-based technologies of the three-color TruCOUNT tube with the FACScan FCM and a two-color FACSCount system (Becton Dickinson Biosciences). Absolute CD4(+) and CD8(+) T-lymphocyte counts in 200 human immunodeficiency virus type 1-seropositive blood specimens were determined. Statistical analysis for correlation and agreement were performed. A high correlation of absolute CD4 counts was shown when those obtained with CyFlow(green) were compared with those obtained with the bead-based three-color TruCOUNT system (R(2)=0.96; mean bias, -69.1 cells/microl; 95% confidence interval [CI], -225.7 to+87.5 cells/microl) and the FACSCount system (R(2)=0.97; mean bias, -40.0 cells/microl; 95% CI, -165.1 to+85.1 cells/microl). The correlation of the CD4(+) T-lymphocyte counts obtained by the two bead-based systems was high (R(2)=0.98). Interestingly, CyFlow(green) yielded CD4(+) T-lymphocyte counts that were 21.8 and 7.2 cells/microl lower than those obtained with the TruCOUNT and the FACSCount systems, respectively, when CD4(+) T-lymphocyte counts were <250 CD4(+) T-lymphocyte counts/microl range or 17.3 and 5.8 cells/microl less, respectively, when CD4(+) T-lymphocyte counts were <200 cells/microl. The single-parameter CyFlow(green) volumetric technology performed well in comparison with the performance of the standard SP bead-based FCM system. However, a multicenter comparative study is needed before this FCM machine is implemented in resource-limited settings.

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