Koehler M, Bubała H
Kliniki Pediatrii i Hematologii Sl. AM Zabrzu.
Pol Tyg Lek. 1992;47(16-17):347-9.
Four children with the acute leukemia are presented. Their blasts shown the presence of 2 cellular lines markers. Coexistence of markers in the blasts was detected with the technique of double staining the blasts from the bone marrow with: alkaline phosphatase-anti-alkaline phosphatase, and peroxidase with the use of monoclonal antibodies series. Analysis of blasts phenotype with monoclonal antibodies confirm the occurrence of leukemias different from the normally programmed cellular line. Deviations of leukemic cells phenotype may be explained with the fact that leukemogenesis is not an absolute block of cells differentiation but combines maturation disorders and proliferation enabling expression normally absent antigens. It confirms the concept of line preservation and presentation of "earlier frozen" phenotype, and explains the occurrence of leukemias in which blasts present phenotype of one line which does not comply with cell differentiation pattern. Further genotypic studies are necessary to clarify pathogenesis and origin of such blasts. Consequently examination of the larger group of patients with hybrid leukemias will enable conclusions concerning prognostic value of such findings and necessity of introduction of the special therapies.
本文报告了4例急性白血病患儿。他们的原始细胞显示存在两种细胞系标志物。通过使用单克隆抗体系列对骨髓原始细胞进行碱性磷酸酶-抗碱性磷酸酶和过氧化物酶双重染色技术,检测到原始细胞中标志物的共存。用单克隆抗体对原始细胞表型进行分析,证实了存在不同于正常编程细胞系的白血病。白血病细胞表型的偏差可以用以下事实来解释:白血病发生并非细胞分化的绝对阻滞,而是结合了成熟障碍和增殖,使得通常不存在的抗原得以表达。这证实了细胞系保留和“早期冻结”表型呈现的概念,并解释了原始细胞呈现不符合细胞分化模式的一个细胞系表型的白血病的发生。需要进一步的基因研究来阐明此类原始细胞的发病机制和起源。因此,对更大组的混合性白血病患者进行检查,将有助于得出关于这些发现的预后价值以及引入特殊治疗必要性的结论。