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利用聚合酶链反应检测T细胞受体γ链V基因重排:在急性淋巴细胞白血病克隆性疾病细胞研究中的应用

Detection of T-cell receptor gamma chain V gene rearrangements using the polymerase chain reaction: application to the study of clonal disease cells in acute lymphoblastic leukemia.

作者信息

Taylor J J, Rowe D, Williamson I K, Christmas S E, Proctor S J, Middleton P G

机构信息

Leukaemia Research Fund Laboratory, Medical School, University of Newcastle upon Tyne, UK.

出版信息

Blood. 1991 May 1;77(9):1989-95.

PMID:1850309
Abstract

This report describes the development and characterization of a method for the amplification of rearranged V-J segments of the human T-cell receptor gamma chain (TCRG) locus using an adaptation of the polymerase chain reaction (PCR) technique. The technique uses a single pair of 'consensus' primers to amplify rearrangements involving the V gamma I subgroup genes, which are common in malignant cells from acute lymphoblastic leukemia (ALL) patients. Using this method we were able to detect rearrangements in the TCRG locus in disease cells from patients with T-cell ALL (12 of 12), common ALL (10 of 14), and Null cell ALL (2 of 2) at presentation. Monoallelic and biallelic rearrangements involving V gamma I subgroup genes were identified by restriction analysis of PCR products from DNA samples from a T-cell leukemic cell line, T-cell clones, and disease cells from patients with ALL of T-and B-cell lineage at presentation. These results confirmed the presence of cell clones within the presentation samples and, in one case, confirmed the persistence of the original malignant cell clone at relapse. This is a rapid and specific method for the detection and characterization of rearrangements of the TCRG locus without recourse to Southern blotting. Therefore, the PCR technique described herein can provide the basis for the study of clonal evolution and minimal residual disease on a high proportion of patients with ALL.

摘要

本报告描述了一种利用聚合酶链反应(PCR)技术的改进方法来扩增人T细胞受体γ链(TCRG)基因座重排的V-J片段的方法及其特性。该技术使用一对“通用”引物来扩增涉及VγI亚组基因的重排,这些基因在急性淋巴细胞白血病(ALL)患者的恶性细胞中很常见。使用这种方法,我们能够在初诊时检测出T细胞ALL患者(12例中的12例)、普通ALL患者(14例中的10例)和无细胞ALL患者(2例中的2例)的疾病细胞中TCRG基因座的重排。通过对来自T细胞白血病细胞系、T细胞克隆以及T细胞和B细胞系ALL患者初诊时疾病细胞的DNA样本的PCR产物进行限制性分析,鉴定出涉及VγI亚组基因的单等位基因和双等位基因重排。这些结果证实了初诊样本中存在细胞克隆,并且在一个病例中,证实了复发时原始恶性细胞克隆的持续存在。这是一种无需进行Southern印迹法即可快速、特异性地检测和鉴定TCRG基因座重排的方法。因此,本文所述的PCR技术可为研究大多数ALL患者的克隆进化和微小残留病提供基础。

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