Butterworth S V, Taylor A M
Int J Cancer. 1987 Jun 15;39(6):678-84. doi: 10.1002/ijc.2910390604.
Ataxia telangiectasia (A-T) is an autosomal recessive disorder in which patients show an unusual predisposition to lymphoid malignancies including T-cell leukaemia. We compare here the surface phenotypes of fresh and cultured A-T T cells. A total of 17 T-cell cultures from 8 A-T patients are compared with each other and with 5 T-cell cultures from normal individuals. The large, cytogenetically abnormal t(14;14) and t(X;14) clones in 2 of the patients both occurred only in the CD8+ population of T lymphocytes. There was no difference in the rate of growth of A-T T cells in vitro compared with those from normal individuals, although many of the original characteristics of the T cells were lost, including the cytogenetically abnormal clones seen in fresh A-T lymphocytes.
共济失调毛细血管扩张症(A-T)是一种常染色体隐性疾病,患者表现出对包括T细胞白血病在内的淋巴恶性肿瘤的异常易感性。我们在此比较新鲜的和培养后的A-T T细胞的表面表型。将来自8名A-T患者的总共17个T细胞培养物相互比较,并与来自正常个体的5个T细胞培养物进行比较。2名患者中出现的大的、细胞遗传学异常的t(14;14)和t(X;14)克隆仅出现在T淋巴细胞的CD8+群体中。与正常个体的T细胞相比,A-T T细胞在体外的生长速率没有差异,尽管T细胞的许多原始特征丧失了,包括在新鲜的A-T淋巴细胞中看到的细胞遗传学异常克隆。