Ikeda T, Kita K, Kawakami K, Ohno T, Seki S, Nasu K, Ueda T, Honjo T, Shirakawa S
Second Department of Internal Medicine, Mie University School of Medicine.
Jpn J Cancer Res. 1990 Apr;81(4):340-4. doi: 10.1111/j.1349-7006.1990.tb02573.x.
The occurrence of more than two rearranged bands of immunoglobulin heavy chain (IgH) genes in B precursor acute lymphoblastic leukemia (ALL) has recently been documented. To elucidate the nature of such leukemias, we studied 30 patients with common ALL, including 6 patients with Philadelphia chromosome (Ph1)-positive ALL, by immunophenotyping and genotyping. In 10 of the 30, Southern blotting showed oligoclonal patterns of IgH gene arrangements, which were frequently detected in Ph1-positive ALL. In one patient of the 10, three rearranged bands of Ig kappa chain genes were detected. Ph1 abnormality and co-expression of myeloid associated antigens were found in 5 and 5 of the 10, respectively. Detection of multiple fragments of IgH genes would be suggestive of multipotent progenitor origin of these ALL.
最近有文献记载,在B前体急性淋巴细胞白血病(ALL)中出现了两条以上免疫球蛋白重链(IgH)基因重排带。为阐明此类白血病的本质,我们通过免疫表型分析和基因分型研究了30例普通ALL患者,其中包括6例费城染色体(Ph1)阳性ALL患者。在30例患者中的10例中,Southern印迹显示IgH基因重排呈寡克隆模式,这种模式在Ph1阳性ALL中经常被检测到。在这10例患者中的1例中,检测到了Igκ链基因的三条重排带。在这10例患者中,分别有5例发现了Ph1异常和5例发现了髓系相关抗原的共表达。检测到IgH基因的多个片段提示这些ALL起源于多能祖细胞。