细胞分析系统基于免疫磁细胞选择和比对,然后使用光盘技术进行免疫荧光分析。

Cytometry Pub Date : 2001-01-01
A G Tibbe, B G de Grooth, J Greve, P A Liberti, G J Dolan, L W Terstappen
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引用次数: 0

摘要

背景:虽然流式细胞仪已成为细胞分析的标准,但它也有局限性。最近,我们介绍了一种新的基于免疫磁选择和细胞对齐的细胞分析方法。不需要流动系统,可以在全血中进行细胞分析。方法:用荧光标记和免疫磁性纳米颗粒孵育全血。血液被注入处于强磁场中的毛细血管。免疫磁标记的细胞向上移动,并沿着毛细血管上表面的铁磁线排列。光学聚焦和跟踪系统类似于传统的光盘播放器,将635纳米激光二极管聚焦在磁排列的细胞上。发射的荧光信号被投射到两个光电倍增管上。采用同种异体藻蓝蛋白(APC)标记的CD4 (CD4-APC)和Cyanin5.5 (Cy5.5)标记的CD8 (CD8-Cy5.5)抗体和Oxazine750作为荧光标记,均为红色激发。结果:CD4-APC与Oxazine750联合使用可获得全血白细胞计数差异。结果与Technicon-H1血液学分析仪进行比较。中性粒细胞相关系数为0.91,淋巴细胞相关系数为0.93,单核细胞相关系数为0.93,嗜酸性粒细胞相关系数为0.96。免疫荧光用CD4-APC和CD8-Cy5.5进行验证。CD4+和CD8+绝对计数与Coulter Epics XL流式细胞仪比较。相关系数分别为0.91和0.94。结论:我们得出的结论是,我们的系统与标准流式细胞仪或血液学分析仪一样能够进行可靠的常规白细胞分析,包括免疫表型分析,并且可以用作易于操作的一次性白细胞测试。
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Cell analysis system based on immunomagnetic cell selection and alignment followed by immunofluorescent analysis using compact disk technologies.

Background: Although the flow cytometer has become the standard in cell analysis, it has limitations. Recently, we introduced a new cell analysis method based on immunomagnetic selection and aligning of cells. No flow system is needed and cell analysis can be performed in whole blood.

Methods: Whole blood is incubated with fluorescent labels and immunomagnetic nanoparticles. The blood is injected into a capillary that is in a strong magnetic field. The immunomagnetic-labeled cells move upward and align themselves along ferromagnetic lines present on the upper surface of the capillary. An optical focus and tracking system analogous to that used in a conventional compact disk player focuses a 635-nm laser-diode on the magnetically aligned cells. The emitted fluorescence signals are projected on two photomultipliers. Allophycocyanin (APC)-labeled CD4 (CD4-APC) and Cyanin5.5 (Cy5.5)-labeled CD8 (CD8-Cy5.5) antibodies and Oxazine750, all red excited, are used as fluorescent labels.

Results: A differential white blood cell count performed in whole blood is obtained using the CD4-APC in combination with Oxazine750. The results are compared with the Technicon-H1 hematology analyzer. Correlation coefficients of 0.91 for neutrophilic granulocytes, 0.93 for lymphocytes, 0.93 for monocytes, and 0.96 for eosinophilic granulocytes were obtained. Immunofluorescence is demonstrated using CD4-APC and CD8-Cy5.5. The absolute counts obtained for CD4+ and CD8+ are compared with the Coulter Epics XL flow cytometer. Correlation coefficients of, respectively, 0.91 and 0.94 were obtained.

Conclusion: We conclude that our system is as capable as a standard flow cytometer or hematology analyzer for a reliable routine white blood cell analysis, including immunophenotyping, and can be used as an easy-to-handle disposable white blood cell test.

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