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白血病巨核细胞系在光镜和电镜水平的免疫特征分析。

Immunological characterization of the leukemic megakaryocytic line at light and electron microscopic levels.

作者信息

Tabilio A, Vainchenker W, Van Haecke D, Vinci G, Guichard J, Henri A, Reyes F, Breton-Gorius J

出版信息

Leuk Res. 1984;8(5):769-81. doi: 10.1016/0145-2126(84)90098-5.

DOI:10.1016/0145-2126(84)90098-5
PMID:6492854
Abstract

Twenty cases of leukemia involving platelet precursors have been identified by a panel of monoclonal and polyclonal antiplatelet antibodies and by the ultrastructural demonstration of platelet peroxidase (PPO). The two techniques were in close agreement both for identification and for the quantitation of the blast cells except in three cases where PPO was present in the absence of the immunological markers. The immunological appearance of the leukemic megakaryocytic precursors was identical to that of their normal counterparts; the cells were positive with J 15 (anti GP IIb-IIIa complex), C 17 (anti GP IIIa), J 2 (anti GP 26,000) AN 51 (anti GP Ib). A diffuse cytoplasmic labelling was observed with anti factor VIII vwF and anti platelet factor 4 (PF 4). In addition, the leukemic maturation was quite similar to normal megakaryocyte differentiation since in micromegakaryocytes the expression of Gp Ib was strong and an intense granular pattern of labelling with anti factor VIII vwF and anti PF 4 was observed. In no case was the leukemic megakaryocytic series labelled by anti-erythroid antibodies, anti myeloid antibodies or J 5, B 1, OKT 11 antibodies. Using ultrastructural immunoferritin with J 15 it was possible to demonstrate that labelling with this antibody only occurred on PPO-positive cells. Immunogold or peroxidase labelling with AN 51 at the EM level in cases of mixed leukemia showed that Gp Ib was absent from proerythroblasts and myeloblasts. Therefore, in no case were specific platelet markers expressed in the leukemias of other cell lineages.

摘要

通过一组单克隆和多克隆抗血小板抗体以及血小板过氧化物酶(PPO)的超微结构显示,已鉴定出20例累及血小板前体的白血病病例。除了3例PPO存在但缺乏免疫标记的情况外,这两种技术在原始细胞的鉴定和定量方面都非常一致。白血病巨核细胞前体的免疫表现与其正常对应物相同;细胞对J 15(抗GP IIb-IIIa复合物)、C 17(抗GP IIIa)、J 2(抗GP 26,000)、AN 51(抗GP Ib)呈阳性。用抗因子VIII vwF和抗血小板因子4(PF 4)观察到弥漫性细胞质标记。此外,白血病成熟与正常巨核细胞分化非常相似,因为在微巨核细胞中,Gp Ib的表达很强,并且观察到用抗因子VIII vwF和抗PF 4标记的强烈颗粒模式。白血病巨核细胞系列均未被抗红细胞抗体、抗髓细胞抗体或J 5、B 1、OKT 11抗体标记。使用带有J 15的超微结构免疫铁蛋白可以证明,用该抗体标记仅发生在PPO阳性细胞上。在混合白血病病例中,在电子显微镜水平用AN 51进行免疫金或过氧化物酶标记显示,早幼红细胞和原粒细胞中不存在Gp Ib。因此,在其他细胞系的白血病中,从未表达过特异性血小板标记物。

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