Li Xiao, Ymeti Aurel, Lunter Björn, Breukers Christian, Tibbe Arjan G J, Terstappen Leon W M M, Greve Jan
University of Twente, Faculty of Science and Technology, Biophysical Engineering Group, Building Zuidhorst, Dienstweg 1, 7522 ND Enschede, The Netherlands.
Cytometry B Clin Cytom. 2007 Sep;72(5):397-407. doi: 10.1002/cyto.b.20165.
HIV monitoring in resource-constrained settings demands affordable and reliable CD4(+) T lymphocytes enumeration methods. We developed a simple single platform image cytometer (SP ICM), which is a dedicated volumetric CD4(+) T lymphocytes enumeration system that uses immunomagnetic and immunofluorescent technologies. The instrument was designed to be a low-cost, yet reliable and robust one. In this article we test the instrument and the immunochemical procedures used on blood from HIV negative and HIV positive patients.
After CD4 immunomagnetic labeling in whole blood, CD4(+) T lymphocytes, CD4(+dim) monocytes and some nonspecifically labeled cells are magnetically attracted to an analysis surface. Combining with CD3-Phycoerythrin (PE) labeling, only CD3(+)CD4(+) T lymphocytes are fluorescently labeled and visible in a fluorescent image of the analysis surface. The number of CD4(+) T lymphocytes is obtained by image analysis. Alternatively, CD3 immunomagnetic selection in combination with CD4 immunofluorescent labeling can also be applied for CD4(+) T lymphocytes enumeration.
The SP ICM system was compared with two single platform flow cytometer (SP FCM) methods: tetraCXP and TruCount methods. The SP ICM system has excellent precision, accuracy and linearity for CD4(+) T lymphocytes enumeration. Good correlations were obtained between the SP ICM and the SP FCM methods for blood specimens of 44 HIV(-) patients, and of 63 HIV(+) patients. Bland-Altman plots showed interchangeability between the SP ICM and the SP FCM methods.
The immunolabeling methods and the instrumentation are simple and easy-to-handle for less-trained operators. The SP ICM system is a good candidate for CD4(+) T lymphocytes enumeration in point-of-care settings of resource-constrained countries.
在资源有限的环境中进行艾滋病毒监测需要经济实惠且可靠的CD4(+) T淋巴细胞计数方法。我们开发了一种简单的单平台图像细胞仪(SP ICM),它是一种专用的体积式CD4(+) T淋巴细胞计数系统,采用免疫磁珠和免疫荧光技术。该仪器设计为低成本但可靠且耐用。在本文中,我们测试了该仪器以及用于HIV阴性和HIV阳性患者血液的免疫化学程序。
在全血中进行CD4免疫磁珠标记后,CD4(+) T淋巴细胞、CD4(+dim)单核细胞和一些非特异性标记的细胞被磁性吸引到分析表面。结合CD3-藻红蛋白(PE)标记,只有CD3(+)CD4(+) T淋巴细胞被荧光标记并在分析表面的荧光图像中可见。通过图像分析获得CD4(+) T淋巴细胞的数量。或者,CD3免疫磁珠分选结合CD4免疫荧光标记也可用于CD4(+) T淋巴细胞计数。
将SP ICM系统与两种单平台流式细胞仪(SP FCM)方法:tetraCXP和TruCount方法进行比较。SP ICM系统在CD4(+) T淋巴细胞计数方面具有出色的精密度、准确性和线性度。对于44例HIV(-)患者和63例HIV(+)患者的血液样本,SP ICM与SP FCM方法之间获得了良好的相关性。Bland-Altman图显示SP ICM和SP FCM方法之间具有互换性。
免疫标记方法和仪器对于训练较少的操作人员来说简单易操作。SP ICM系统是资源有限国家即时检测环境中CD4(+) T淋巴细胞计数的良好选择。