Tesch H, Fonatsch C, Diehl V
I. Medizinische Klinik, Universität Köln, FRG.
In Vivo. 1991 May-Jun;5(3):233-8.
Clonal rearrangements of immunoglobulin (Ig) and T cell receptor (TCR) genes have been demonstrated in malignant lymphoid tumors of B and T cell origin. In Philadelphia chromosome (Ph1) positive chronic myeloid leukemia (CML) the bcr and c-abl genes are reorganized and a new transcript, composed of both genes is expressed. Immunoglobulin gene rearrangements were also detected in lymphoid blast crisis but not in myeloid blast crisis of CML. We analyzed in Southern blot experiments whether Ig and TCR rearrangements could also occur in the chronic or accelerated phase of the disease. Our results indicate that immunoglobulin but not TCR delta or TCR gamma gene rearrangements also occurred in some patients with CML in chronic and accelerated phase but not in myeloid blast crisis, together with rearrangements of the bcr gene.
免疫球蛋白(Ig)和T细胞受体(TCR)基因的克隆重排在B细胞和T细胞起源的恶性淋巴瘤中已得到证实。在费城染色体(Ph1)阳性的慢性髓性白血病(CML)中,bcr和c-abl基因发生重排,由这两个基因组成的新转录本得以表达。免疫球蛋白基因重排在CML的淋巴细胞母细胞危象中也可检测到,但在髓细胞母细胞危象中未检测到。我们通过Southern印迹实验分析了Ig和TCR重排在疾病的慢性期或加速期是否也会发生。我们的结果表明,在一些慢性期和加速期的CML患者中也发生了免疫球蛋白基因重排,而非TCRδ或TCRγ基因重排,且在髓细胞母细胞危象中未发生,同时还伴有bcr基因重排。