van der Velden Vincent H J, van Dongen Jacques J M
Department of Immunology, Erasmus MC, Erasmus University Medical Center, Rotterdam, The Netherlands.
Methods Mol Biol. 2009;538:115-50. doi: 10.1007/978-1-59745-418-6_7.
Minimal residual disease (MRD) diagnostics has proven to be clinically relevant for evaluation of treatment effectiveness in patients with acute lymphoblastic leukemia (ALL). In most ALL treatment protocols, MRD diagnostics is performed by real-time quantitative PCR (RQ-PCR) analysis of the junctional regions of rearranged immunoglobulin (Ig) and T-cell receptor (TCR) genes.MRD diagnostics via Ig/TCR genes is broadly applicable (>95% of ALL patients) and can reach a good sensitivity (< or =10 (-4)). However, the technique is complex and requires extensive knowledge and experience, because the junctional regions of each leukemia have to be identified before the patient-specific RQ-PCR assays can be designed for MRD monitoring. This chapter provides all relevant background information and technical aspects for the complete laboratory process from detection of the clonal Ig/TCR gene rearrangements in ALL cells at diagnosis to the actual MRD measurements in clinical follow-up samples. This information aims at facilitating the PCR-based MRD diagnostics in ALL patients. However, it should be noted that MRD diagnostics for clinical treatment protocols has to be accompanied by regular international quality control rounds to ensure the reproducibility and reliability of the MRD results.
微小残留病(MRD)诊断已被证明在评估急性淋巴细胞白血病(ALL)患者的治疗效果方面具有临床相关性。在大多数ALL治疗方案中,MRD诊断是通过对重排的免疫球蛋白(Ig)和T细胞受体(TCR)基因的连接区进行实时定量PCR(RQ-PCR)分析来进行的。通过Ig/TCR基因进行MRD诊断具有广泛的适用性(>95%的ALL患者),并且可以达到良好的灵敏度(≤10⁻⁴)。然而,该技术复杂,需要广泛的知识和经验,因为在设计用于MRD监测的患者特异性RQ-PCR检测之前,必须先确定每种白血病的连接区。本章提供了从诊断时检测ALL细胞中的克隆性Ig/TCR基因重排到临床随访样本中实际MRD测量的完整实验室过程的所有相关背景信息和技术方面。这些信息旨在促进ALL患者基于PCR的MRD诊断。然而,应该注意的是,临床治疗方案的MRD诊断必须伴随着定期的国际质量控制轮次,以确保MRD结果的可重复性和可靠性。