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黄巧容, 蒋燕妮, 李慧芳, 等. 14色流式检测人外周血白细胞亚群方案的建立[J]. 四川大学学报(医学版), 2022, 53(1): 127-132. DOI: 10.12182/20220160106
引用本文: 黄巧容, 蒋燕妮, 李慧芳, 等. 14色流式检测人外周血白细胞亚群方案的建立[J]. 四川大学学报(医学版), 2022, 53(1): 127-132. DOI: 10.12182/20220160106
HUANG Qiao-rong, JIANG Yan-ni, LI Hui-fang, et al. Establishment of 14-Color Panel for Determining Leukocyte Subsets in Human Peripheral Blood with Flow Cytometry[J]. Journal of Sichuan University (Medical Sciences), 2022, 53(1): 127-132. DOI: 10.12182/20220160106
Citation: HUANG Qiao-rong, JIANG Yan-ni, LI Hui-fang, et al. Establishment of 14-Color Panel for Determining Leukocyte Subsets in Human Peripheral Blood with Flow Cytometry[J]. Journal of Sichuan University (Medical Sciences), 2022, 53(1): 127-132. DOI: 10.12182/20220160106

14色流式检测人外周血白细胞亚群方案的建立

Establishment of 14-Color Panel for Determining Leukocyte Subsets in Human Peripheral Blood with Flow Cytometry

    摘要
  • 摘要:
      目的  建立14色流式检测人外周血中白细胞亚群方案。
      方法  用细胞膜表面抗体CD45、CD3、CD4、CD8、CD19、CD56、CD16、CD14、CD25、CD127、HLA-DR、CD123、 CD11c和核酸染料DAPI建立14色流式染色方案,检测人外周血白细胞主要细胞亚群。取健康成年志愿者外周血标本分别对各抗体进行抗体滴度实验、光电倍增管(photomultiplier tube, PMT)电压优化、单色染色和减一色染色,确定检测方法和检测条件后,对18例健康成年志愿者外周血标本进行检测分析。
      结果  根据细胞分群情况和染色指数选择抗体最适质量浓度:CD25和CD127为8.0 μg/mL;CD45、CD3、CD14和CD123为4.0 μg/mL;CD8、CD19、CD56、CD16、HLA-DR和CD11c为2.0 μg/mL;CD4为1.0 μg/mL;DAPI使用质量浓度为0.1 μg/mL。CD45、CD3、CD4、CD8、CD19、CD56、CD16、CD14、CD25、CD127、HLA-DR、CD123、CD11c和DAPI检测电压分别为:450 V、410 V、400 V、550 V、405V、500 V、520 V、550 V、550 V、400 V、450 V、400 V、580 V和300 V。单色染色和减一色试验确定合适的荧光补偿。采用建立的14色流式检测人外周血白细胞主要亚群的方案检测了18例健康成年人外周血样本,可分析出外周血中各细胞亚群在白细胞中的百分比,以及主要细胞群的免疫表型。
      结论  成功建立14色流式检测人外周血白细胞亚群方案,结果稳定可靠,操作简便。

     

    Abstract:
      Objective  To establish a 14-color flow cytometry protocol for the examination of leukocyte subsets in human peripheral blood.
      Methods  We used cell membrane surface antibodies CD45, CD3, CD4, CD8, CD19, CD56, CD16, CD14, CD25, CD127, HLA-DR, CD123, CD11c and nucleus staining dye DAPI to establish a 14-color flow cytometry assay to determine the major cell subsets in human peripheral blood. We collected peripheral blood specimens from healthy volunteers to test for antibody titers and optimal photomultiplier tube (PMT) voltage, and to conduct single-color staining and fluorescence minus one control staining. After determining the test method and test conditions, the peripheral blood samples of 18 healthy volunteers were analyzed.
      Results  According to the cell classification and staining index, optimal antibody mass concentrations selected were as follows: CD25 and CD127 at 8.0 μg/mL, CD45, CD3, CD14 and CD123 at 4.0 μg/mL, CD8, CD19, CD56, CD16, HLA-DR and CD11c at 2.0 μg/mL, CD4 at 1.0 μg/mL and DAPI at 0.1 μg/mL. The detection voltages for CD45, CD3, CD4, CD8, CD19, CD56, CD16, CD14, CD25, CD127, HLA-DR, CD123, CD11c and DAPI were 450 V, 410 V, 400 V, 550 V, 405 V, 500 V, 520 V, 550 V, 550 V, 400 V, 450 V, 400 V, 580 V, and 300 V, respectively. The appropriate fluorescence compensation was determined by single-color staining and fluorescence minus one controls. The 14-color flow cytometry panel was established to analyze the main subsets of leukocytes in human peripheral blood, and peripheral blood samples from 18 healthy adults were examined, obtaining the percentages of each subset of peripheral blood leukocytes and the immunophenotypes of the main subsets.
      Conclusion  We established a 14-color panel for determining leukocyte subsets in human peripheral blood by flow cytometry, which produced stable and reliable results and was easy to operate.

     

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