Valiron O, Clemancey-Marcille G, Troesch A, Schweitzer A, Prenant M, Hollard D, Berthier R
INSERM U217, Laboratoire d'Hématologie, Grenoble, France.
Leuk Res. 1988;12(10):861-72. doi: 10.1016/0145-2126(88)90040-9.
The immunophenotype of peripheral blood blast cells from 14 patients in the chronic phase of chronic myeloid leukemia (CML) was studied using a panel of monoclonal antibodies (McAb) directed against megakaryocytic, granulomonocytic, erythroid and lymphoid antigenic determinants. The blast cells were enriched by a simple bovine serum albumin (BSA) density-cut separation and cooled in liquid nitrogen. The study was done using the alkaline phosphatase-anti-alkaline phosphatase (APAAP) technique on the thawed blast cells. A consistent pattern of reactivity with McAb was found in all patients, showing that blast cells were heterogeneous. A minor component of the blast cells react with platelet antibodies, most of them being labelled with anti-GPIIb-IIIa McAb. Anti-GPIb and Von Willebrand factor McAb detected 4 times fewer megakaryocytic blast cells, suggesting that these cells are located very early in the differentiation scheme. Two major blast cell compartments were labelled with early myelomonocytic (anti-CD13: MY7) and early erythroid (anti-CD36: FA6-152) McAb. The CD34 (My10) and DR antigens which are expressed by immature blast cells and myeloid progenitors of human bone marrow (BM) were present on more than 50% of the CML blast cells. Thus, the blast cells of chronic phase CML patients, showed the same cellular diversity as the increased progenitor cell compartment observed in this disease, and their differentiation stages seemed to be very closely related.
利用一组针对巨核细胞、粒单核细胞、红系细胞和淋巴系抗原决定簇的单克隆抗体(McAb),对14例慢性髓系白血病(CML)慢性期患者外周血原始细胞的免疫表型进行了研究。通过简单的牛血清白蛋白(BSA)密度梯度分离富集原始细胞,并在液氮中冷冻。采用碱性磷酸酶-抗碱性磷酸酶(APAAP)技术对解冻后的原始细胞进行研究。在所有患者中均发现了与McAb一致的反应模式,表明原始细胞具有异质性。原始细胞的一小部分与血小板抗体反应,其中大多数被抗GPIIb-IIIa McAb标记。抗GPIb和血管性血友病因子McAb检测到的巨核细胞原始细胞减少了4倍,这表明这些细胞在分化过程中处于非常早期的阶段。两个主要的原始细胞亚群分别被早期粒单核细胞(抗CD13:MY7)和早期红系细胞(抗CD36:FA6-152)McAb标记。人骨髓(BM)中未成熟原始细胞和髓系祖细胞表达的CD34(My10)和DR抗原在超过50%的CML原始细胞中存在。因此,CML慢性期患者的原始细胞表现出与该疾病中观察到的祖细胞增加亚群相同的细胞多样性,并且它们的分化阶段似乎密切相关。