Tozzo Pamela, Delicati Arianna, Zambello Renato, Caenazzo Luciana
Department of Molecular Medicine, Laboratory of Forensic Genetics, University of Padova, 35121 Padova, Italy.
Department of Medicine (DIMED), Hematology and Clinical Immunology Section, Padova University School of Medicine, 35121 Padova, Italy.
Diagnostics (Basel). 2021 Mar 30;11(4):621. doi: 10.3390/diagnostics11040621.
Chimerism analysis is a well-established method for monitoring the state of hematopoietic stem cell transplantation (HSCT) over time by analyzing peripheral blood or bone marrow samples of the recipient in several malignant and non-malignant hematologic diseases. From a clinical point of view, a continuous monitoring is fundamental for an effective early therapeutic intervention. This paper provides a comparative overview of the main molecular biology techniques which can be used to study chimerism after bone marrow transplantation, focusing on their advantages and disadvantages. According to the examined literature, short tandem repeats (STR) analysis through simple PCR coupled with capillary electrophoresis (STR-PCR) is the most powerful method which guarantees a high power of differentiation between different individuals. However, other methods such as real-time quantitative PCR (qPCR), digital PCR (dPCR), and next-generation sequencing (NGS) technology were developed to overcome the technical limits of STR-PCR. In particular, these other techniques guarantee a higher sensitivity, which allows for the detection of chimerism at an earlier stage, hence expanding the window for therapeutic intervention. After a comparative evaluation of the various techniques, it seems clear that STR-PCR still remains the gold standard option for chimerism study, even if it is likely that both dPCR and NGS could supplement or even replace the common methods of STR analysis.
嵌合体分析是一种成熟的方法,通过分析多种恶性和非恶性血液疾病患者外周血或骨髓样本,来长期监测造血干细胞移植(HSCT)的状态。从临床角度来看,持续监测对于有效的早期治疗干预至关重要。本文对可用于研究骨髓移植后嵌合体的主要分子生物学技术进行了比较综述,重点介绍了它们的优缺点。根据所查阅的文献,通过简单PCR结合毛细管电泳进行短串联重复序列(STR)分析(STR-PCR)是最强大的方法,能确保在不同个体之间有很高的区分能力。然而,为克服STR-PCR的技术局限,还开发了其他方法,如实时光定量PCR(qPCR)、数字PCR(dPCR)和下一代测序(NGS)技术。特别是,这些其他技术具有更高的灵敏度,能够在更早阶段检测到嵌合体,从而扩大治疗干预的窗口期。在对各种技术进行比较评估后,很明显STR-PCR仍然是嵌合体研究的金标准选择,即使dPCR和NGS都有可能补充甚至取代STR分析的常用方法。