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骨髓或外周血干细胞移植后慢性粒细胞白血病中使用实时逆转录聚合酶链反应监测BCR-ABL表达

Monitoring of BCR-ABL expression using real-time RT-PCR in CML after bone marrow or peripheral blood stem cell transplantation.

作者信息

Eder M, Battmer K, Kafert S, Stucki A, Ganser A, Hertenstein B

机构信息

Medizinische Hochschule Hannover, Abteilung Hämatologie und Onkologie, Zentrum der Inneren Medizin, Germany.

出版信息

Leukemia. 1999 Sep;13(9):1383-9. doi: 10.1038/sj.leu.2401489.

Abstract

To analyze the value of real time RT-PCR for monitoring of bcr-abl expression in CML patients after allogeneic or autologous stem cell transplantation (SCT), we generated pairs of PCR-primers and TaqMan probes specific for either the b2a2- or the b3a2-variant of bcr-abl. Either variant could be detected specifically from cDNA from a single K562 (b3a2) and BV173 (b2a2) cell with the respective TaqMan probe. Bcr-abl expression was normalized by comparison with GAPDH expression, and samples were quantitated using standard cDNA dilutions from K562 or BV173 cells. In a retrospective analysis 13 patients with CML after allogeneic (n = 10) or autologous (n = 3) SCT including patients with relapsed or persistent CML were analyzed by both real-time and conventional nested RT-PCR. In addition chimerism was monitored by FISH analysis of sex chromosomes in three patients with relapsed disease. The bcr-abl/GAPDH ratio dropped at least 1000-fold in all seven patients evaluable prior to and after allogeneic SCT as estimated by real-time RT-PCR, and conventional RT-PCR became negative in 6/7 patients. In five patients with relapsed or persistent disease after allogeneic SCT the bcr-abl/GAPDH ratio eventually increased again, and real-time RT-PCR was as sensitive as conventional RT-PCR for detection of bcr-abl. Donor lymphocyte infusions (DLI) were given to all five patients, and the bcr-abl/GAPDH ratio dropped to undetectable levels in two patients both remaining in continuing molecular remission. In contrast, in three other patients the bcr-abl/GAPDH ratio decreased only or did not change significantly after DLI. In three patients undergoing autologous SCT the bcr-abl/GAPDH ratio dropped only 1.1 to 30-fold, and the patients were tested positive with real-time RT-PCR at all time points. These data demonstrate that real-time RT-PCR is valuable to quantitate bcr-abl expression in CML patients after transplantation.

摘要

为分析实时逆转录聚合酶链反应(RT-PCR)在监测异基因或自体干细胞移植(SCT)后慢性粒细胞白血病(CML)患者bcr-abl表达中的价值,我们制备了针对bcr-abl的b2a2或b3a2变异体的PCR引物对和TaqMan探针。使用各自的TaqMan探针,可从单个K562(b3a2)和BV173(b2a2)细胞的cDNA中特异性检测到任一变异体。通过与甘油醛-3-磷酸脱氢酶(GAPDH)表达进行比较来标准化bcr-abl表达,并使用来自K562或BV173细胞的标准cDNA稀释液对样本进行定量。在一项回顾性分析中,对13例异基因(n = 10)或自体(n = 3)SCT后的CML患者(包括复发或持续性CML患者)进行了实时和传统巢式RT-PCR分析。此外,对3例复发疾病患者通过性染色体荧光原位杂交(FISH)分析监测了嵌合情况。通过实时RT-PCR估计,在所有7例异基因SCT前后可评估的患者中,bcr-abl/GAPDH比值至少下降了1000倍,并且传统RT-PCR在6/7例患者中变为阴性。在5例异基因SCT后复发或持续性疾病的患者中,bcr-abl/GAPDH比值最终再次升高,并且实时RT-PCR在检测bcr-abl方面与传统RT-PCR一样敏感。对所有5例患者进行了供体淋巴细胞输注(DLI),2例患者的bcr-abl/GAPDH比值降至不可检测水平,二者均保持持续分子缓解状态。相比之下,在其他3例患者中,DLI后bcr-abl/GAPDH比值仅下降或未显著变化。在3例接受自体SCT的患者中,bcr-abl/GAPDH比值仅下降了1.1至30倍,并且这些患者在所有时间点的实时RT-PCR检测均为阳性。这些数据表明,实时RT-PCR在定量移植后CML患者的bcr-abl表达方面具有重要价值。

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