Koníková E, Babusíková O, Mesárosová A, Kusenda J, Glasová M
Cancer Research Institute, Slovak Academy of Sciences, Bratislava.
Neoplasma. 1994;41(2):69-74.
Peripheral blood cells of twenty-six patients with B cell chronic lymphocytic leukemia (B-CLL) were characterized for their surface membrane and cytoplasmic marker profiles using flow cytometry and fluorescence microscopy. According to surface membrane marker analysis three distinct immunophenotypic subgroups of B-CLL were identified: group I (SIg+, MR+, CD5+, B Ag+, T Ag-; 19 cases), group II (SIg+, MR+, CD5+, B Ag+, TAg+; 3 cases), group III (SIg-, MR+, CD5+, B Ag+, T Ag-; 4 cases). Cells from all patients were positive for the CD19 antigen and at least one of other B cell antigens. Cells from all patients expressed also CD5 and HLA-DR antigens and formed mouse rosettes (MR). Great heterogeneity was found in the membrane and cytoplasmic marking by anti-CD22 MoAb. In four of 23 patients tested, CD22 antigen was expressed in the cytoplasm of CLL cells while it was absent on surface membrane of these cells. This finding was discussed from the point of certain cell heterogeneity in the followed B-CLL cases. Cytoplasmic immunoglobulin (CyIg) detection showed to be very important especially in group III of followed B-CLL cases with undetectable surface immunoglobulins (SIg). Cytoplasmic antigens and immunoglobulin determinations are useful in phenotyping every B-CLL patient, as well as in the immunological study of different maturation stages of B lymphocytes.
采用流式细胞术和荧光显微镜对26例B细胞慢性淋巴细胞白血病(B-CLL)患者的外周血细胞进行表面膜和细胞质标志物谱分析。根据表面膜标志物分析,确定了B-CLL的三个不同免疫表型亚组:I组(SIg+、MR+、CD5+、B Ag+、T Ag-;19例),II组(SIg+、MR+、CD5+、B Ag+、TAg+;3例),III组(SIg-、MR+、CD5+、B Ag+、T Ag-;4例)。所有患者的细胞CD19抗原及至少一种其他B细胞抗原呈阳性。所有患者的细胞也表达CD5和HLA-DR抗原,并形成小鼠玫瑰花结(MR)。抗CD22单克隆抗体对膜和细胞质的标记显示出很大的异质性。在23例检测患者中的4例中,CD22抗原在CLL细胞的细胞质中表达,而在这些细胞的表面膜上不存在。从所观察的B-CLL病例中某些细胞异质性的角度对这一发现进行了讨论。细胞质免疫球蛋白(CyIg)检测显示非常重要,尤其是在表面免疫球蛋白(SIg)检测不到的所观察的B-CLL病例III组中。细胞质抗原和免疫球蛋白测定对于每个B-CLL患者的表型分析以及B淋巴细胞不同成熟阶段的免疫学研究都很有用。