Ha K, Minden M, Hozumi N, Gelfand E W
Leuk Res. 1986;10(1):1-8. doi: 10.1016/0145-2126(86)90098-6.
By using a panel of monoclonal antibodies in combination with conventional morphological and histochemical studies, seven leukemic patients were diagnosed as having T-cell lymphocytic leukemia (ALL) and three patients were classified as having acute undifferentiated leukemia (AUL). When genomic DNA from each patient was analysed by the Southern blot hybridization technique, two out of seven cases with T-cell ALL and two of three cases with AUL demonstrated immunoglobulin (Ig) mu gene rearrangements. Interestingly, the patterns of C mu gene rearrangement found in these four cases as well as in the T-cell line HSB-2 were quite similar with rearrangement of a single allele and germ line configuration retained in the other allele. Ig gene rearrangement is an essential property of cells of B-lineage, but detection of an Ig gene rearrangement by itself seems insufficient to assign commitment to B-lineage differentiation. The significance of Ig gene rearrangements in T-cell ALL is unclear, but this heterogeneity at the DNA level among T-cell ALL may reflect differences in leukemogeneis and have prognostic and therapeutic implications.
通过使用一组单克隆抗体并结合传统的形态学和组织化学研究,7例白血病患者被诊断为T细胞淋巴细胞白血病(ALL),3例患者被归类为急性未分化白血病(AUL)。当通过Southern印迹杂交技术分析每位患者的基因组DNA时,7例T细胞ALL患者中有2例以及3例AUL患者中有2例显示出免疫球蛋白(Ig)μ基因重排。有趣的是,在这4例病例以及T细胞系HSB-2中发现的Cμ基因重排模式非常相似,单个等位基因发生重排,另一个等位基因保留种系构型。Ig基因重排是B系细胞的一个基本特性,但仅检测到Ig基因重排似乎不足以确定细胞已向B系分化。Ig基因重排在T细胞ALL中的意义尚不清楚,但T细胞ALL在DNA水平上的这种异质性可能反映了白血病发生过程中的差异,并具有预后和治疗意义。