Bregni M, Siena S, Subar M, Villa S, Bonadonna G, Dalla-Favera R, Gianni A M
Haematologica. 1989 Jan-Feb;74(1):11-4.
A patient with T-cell acute lymphoblastic leukemia (T-ALL) in second remission was treated with high doses of chemotherapy and radiotherapy, followed by transplantation of autologous bone marrow purged ex-vivo with an anti-CD5-saporin immunotoxin (OKT1-SAP). Prior to transplantation the bone marrow graft had been considered in complete remission, as assessed by morphology and immunophenotyping. Twenty-two days after transplantation, the disease relapsed in the bone marrow with the same phenotype as at the onset. Retrospective analysis of the transplanted marrow cells by a recently developed high sensitivity and specificity assay (HSS assay), involving immunologic fractionation and T-cell receptor rearrangement analysis, revealed a graft contamination of approximately 0.5% malignant T-cells. This finding, together with the early post-transplant leukemic relapse, strongly suggests that the bone marrow was the source of the leukemic cells. The data are discussed for their implications on residual leukemia detection by gene rearrangement studies.
一名处于第二次缓解期的T细胞急性淋巴细胞白血病(T-ALL)患者接受了高剂量化疗和放疗,随后进行了用抗CD5-皂草素免疫毒素(OKT1-SAP)体外净化的自体骨髓移植。移植前,通过形态学和免疫表型评估,骨髓移植物被认为处于完全缓解状态。移植后22天,骨髓中疾病复发,其表型与发病时相同。通过最近开发的一种高灵敏度和特异性检测方法(HSS检测)对移植的骨髓细胞进行回顾性分析,该方法涉及免疫分离和T细胞受体重排分析,结果显示存在约0.5%的恶性T细胞移植物污染。这一发现,连同移植后早期的白血病复发,强烈提示骨髓是白血病细胞的来源。讨论了这些数据对通过基因重排研究检测残留白血病的意义。