Pongers-Willemse M J, Seriu T, Stolz F, d'Aniello E, Gameiro P, Pisa P, Gonzalez M, Bartram C R, Panzer-Grümayer E R, Biondi A, San Miguel J F, van Dongen J J
Department of Immunology, University Hospital Rotterdam/Erasmus University Rotterdam, The Netherlands.
Leukemia. 1999 Jan;13(1):110-8. doi: 10.1038/sj.leu.2401245.
It is now widely accepted that the detection of minimal residual disease (MRD) has prognostic value in acute leukemia. However clinical MRD studies need standardized techniques. Therefore, several European laboratories have aligned their goals and performed comparative studies to achieve optimization and standardization of MRD techniques. This was achieved via the BIOMED-1 Concerted Action "Investigation of minimal residual disease in acute leukemia: International standardization and clinical evaluation." This report describes the development of PCR primers and protocols for the detection of MRD in acute lymphoblastic leukemia (ALL) using clone-specific junctional regions of immunoglobulin and T cell receptor gene rearrangements and TAL1 deletions as PCR targets. A total of 54 primers was developed (1) to amplify rearrangements of the TCRD, TCRG, and IGK (Kde) genes as well as TAL1 deletions; (2) to sequence the junctional regions and breakpoint fusion regions; and (3) to perform MRD detection in bone marrow or peripheral blood samples during follow-up of ALL patients. Protocols were established to identify PCR targets at diagnosis by performing 25 PCR reactions per patient using appropriate positive and negative controls. Standardized protocols were developed for MRD monitoring via single amplification of the PCR target followed by dot blot hybridization with the corresponding patient-specific junctional region probe. In addition, alternative approaches were designed for cases where the target sensitivity of at least 10(-4) was not obtained. The standardization described here of MRD-PCR techniques is essential for the process of translating MRD research into clinical practice.
目前,人们普遍认为微小残留病(MRD)的检测在急性白血病中具有预后价值。然而,临床MRD研究需要标准化技术。因此,一些欧洲实验室已统一目标并开展比较研究,以实现MRD技术的优化和标准化。这是通过BIOMED-1协同行动“急性白血病微小残留病的研究:国际标准化和临床评估”实现的。本报告描述了用于检测急性淋巴细胞白血病(ALL)中MRD的PCR引物和方案的开发,该方案使用免疫球蛋白和T细胞受体基因重排的克隆特异性连接区以及TAL1缺失作为PCR靶点。共开发了54种引物:(1)用于扩增TCRD、TCRG和IGK(Kde)基因的重排以及TAL1缺失;(2)对连接区和断点融合区进行测序;(3)在ALL患者随访期间对骨髓或外周血样本进行MRD检测。建立了相关方案,通过对每位患者进行25次PCR反应并使用适当的阳性和阴性对照,在诊断时鉴定PCR靶点。开发了标准化方案,通过对PCR靶点进行单扩增,然后与相应的患者特异性连接区探针进行斑点杂交来监测MRD。此外,还针对未获得至少10^(-4)的靶点敏感性的情况设计了替代方法。本文所述的MRD-PCR技术标准化对于将MRD研究转化为临床实践的过程至关重要。