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健康个体和阵发性睡眠性血红蛋白尿症患者淋巴细胞亚群中衰变加速因子和CD59的表达

Expression of decay-accelerating factor and CD59 in lymphocyte subsets of healthy individuals and paroxysmal nocturnal hemoglobinuria patients.

作者信息

Nagakura S, Nakakuma H, Horikawa K, Hidaka M, Kagimoto T, Kawakita M, Tomita M, Takatsuki K

机构信息

Second Department of Internal Medicine, Kumamoto University School of Medicine, Japan.

出版信息

Am J Hematol. 1993 May;43(1):14-8. doi: 10.1002/ajh.2830430105.

DOI:10.1002/ajh.2830430105
PMID:7686331
Abstract

The expression of phosphatidylinositol (PI)-anchored complement-regulatory membrane proteins on circulating blood cells has been well clarified; however, the PI proteins on lymphocyte subsets have not been fully analyzed yet. We examined the expression of decay-accelerating factor (DAF) and CD59 on the T lymphocytes (CD2+, CD3+, CD4+, and CD8+) and CD20+ B lymphocytes in ten healthy volunteers and 12 paroxysmal nocturnal hemoglobinuria (PNH) patients by cytofluorometry. In healthy controls, each subset of lymphocytes showed a small population of cells weakly positive and a large population of cells strongly positive for DAF and CD59, while erythrocytes showed a single population of cells positive for the PI proteins. The two-population expression of DAF was most distinctive in CD8+ T cells among the subsets. In PNH, each subset of lymphocytes showed a moderately higher population of cells weakly positive and a smaller population of cells strongly positive for the membrane proteins compared with those in the healthy controls. Moreover, in some PNH cases, a negative population for the proteins was found in all subsets. Thus the analysis of PI-anchored proteins on lymphocytes subsets (especially CD8+ T cells) was considered to be of diagnostic value in PNH patients who receive blood transfusion after hemolytic attack of affected erythrocytes. Furthermore, the two-population expression of PI proteins in normal lymphocytes suggests that membrane PI protein would be a new subset marker of lymphocytes.

摘要

循环血细胞上磷脂酰肌醇(PI)锚定的补体调节膜蛋白的表达已得到充分阐明;然而,淋巴细胞亚群上的PI蛋白尚未得到充分分析。我们通过细胞荧光测定法检测了10名健康志愿者和12名阵发性夜间血红蛋白尿(PNH)患者的T淋巴细胞(CD2 +、CD3 +、CD4 +和CD8 +)及CD20 + B淋巴细胞上衰变加速因子(DAF)和CD59的表达。在健康对照中,淋巴细胞的每个亚群均显示一小部分细胞DAF和CD59弱阳性,而大部分细胞强阳性,而红细胞则显示单一群体的细胞PI蛋白阳性。在各亚群中,DAF的双群体表达在CD8 + T细胞中最为明显。在PNH患者中,与健康对照相比,淋巴细胞的每个亚群均显示膜蛋白弱阳性的细胞群体略多,而强阳性的细胞群体略少。此外,在一些PNH病例中,所有亚群均发现了蛋白阴性群体。因此,淋巴细胞亚群(尤其是CD8 + T细胞)上PI锚定蛋白的分析被认为对受影响红细胞溶血发作后接受输血的PNH患者具有诊断价值。此外,正常淋巴细胞中PI蛋白的双群体表达表明膜PI蛋白可能是淋巴细胞的一种新的亚群标志物。

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