Maruyama F, Ino T, Miyazaki H, Wakita M, Maeda H, Tsuzuki M, Kojima H, Sobue R, Okamoto M, Matsui T
Department of Internal Medicine, Fujita Health University.
Rinsho Ketsueki. 1993 Jan;34(1):1-6.
We analyzed immunoglobulin (Ig) gene rearrangements in 69 patients with B-cell malignancies by Southern hybridization. We used 5 probes which covered JH 5'S mu and S gamma 3 loci of the Ig heavy (IgH) chain gene, and C kappa and kappa de loci of the Ig light (IgL) chain kappa gene, respectively. DNA rearrangements were observed in 68 out of the 69 patients using the JH probe. In 97% (33/34) of patients with non-Hodgkin's lymphoma (NHL), 100% (5/5) of chronic lymphocytic leukemia (CLL), 42% (10/24) of non-T cell acute lymphoblastic leukemia (non-T ALL), and in 0% (0/4) of chronic myelogenous leukemia lymphoid crisis (CML-LBC), the rearrangements were detected by C kappa and/or kappa de probes. Furthermore, the genotype of the light chain was defined by rearrangement patterns of these 2 probes. The by using the 5'S mu-probe, class switch recombinations were detected in 76% (25/33) of NHL, 20% (1/5) of CLL, 17% (4/24) of non-T ALL, and in 0% (0/4) of CML-LBC. Among them, 1 case of IgM NHL and 3 cases of double bearer NHL had rearranged on both IgH alleles by the constant region. The results of this study indicate that genotypes correspond well to phenotypes of B-cell malignancies and that the determination of genotype will be useful for making an exact diagnosis of B-cell malignancies.
我们通过Southern杂交分析了69例B细胞恶性肿瘤患者的免疫球蛋白(Ig)基因重排。我们使用了5种探针,分别覆盖Ig重链(IgH)基因的JH、5'Sμ和Sγ3位点,以及Ig轻链κ基因的Cκ和κde位点。使用JH探针时,69例患者中有68例观察到DNA重排。在97%(33/34)的非霍奇金淋巴瘤(NHL)患者、100%(5/5)的慢性淋巴细胞白血病(CLL)患者、42%(10/24)的非T细胞急性淋巴细胞白血病(非T-ALL)患者以及0%(0/4)的慢性粒细胞白血病淋巴细胞危象(CML-LBC)患者中,通过Cκ和/或κde探针检测到重排。此外,轻链的基因型由这两种探针的重排模式确定。使用5'Sμ探针时,在76%(25/33)的NHL、20%(1/5)的CLL、17%(4/24)的非T-ALL以及0%(0/4)的CML-LBC中检测到类别转换重排。其中,1例IgM NHL和3例双表达NHL在两个IgH等位基因的恒定区均发生了重排。本研究结果表明,基因型与B细胞恶性肿瘤的表型高度对应,基因型的确定将有助于准确诊断B细胞恶性肿瘤。