Children's Cancer Research Institute and Department of Pediatrics, Meduniwien, Vienna, Austria.
Leukemia. 2012 Aug;26(8):1821-8. doi: 10.1038/leu.2012.66. Epub 2012 Mar 7.
Hematopoietic stem cell transplantation is becoming an increasingly important approach to treatment of different malignant and non-malignant disorders. There is thus growing demand for diagnostic assays permitting the surveillance of donor/recipient chimerism posttransplant. Current techniques are heterogeneous, rendering uniform evaluation and comparison of diagnostic results between centers difficult. Leading laboratories from 10 European countries have therefore performed a collaborative study supported by a European grant, the EuroChimerism Concerted Action, with the aim to develop a standardized diagnostic methodology for the detection and monitoring of chimerism in patients undergoing allogeneic stem cell transplantation. Following extensive analysis of a large set of microsatellite/short tandem repeat (STR) loci, the EuroChimerism (EUC) panel comprising 13 STR markers was established with the aim to optimally meet the specific requirements of quantitative chimerism analysis. Based on highly stringent selection criteria, the EUC panel provides multiple informative markers in any transplant setting. The standardized STR-PCR tests permit detection of donor- or recipient-derived cells at a sensitivity ranging between 0.8 and 1.6%. Moreover, the EUC assay facilitates accurate and reproducible quantification of donor and recipient hematopoietic cells. Wide use of the European-harmonized protocol for chimerism analysis presented will provide a basis for optimal diagnostic support and timely treatment decisions.
造血干细胞移植正成为治疗各种恶性和非恶性疾病的一种越来越重要的方法。因此,对允许在移植后监测供体/受者嵌合体的诊断检测的需求不断增长。目前的技术具有异质性,使得中心之间对诊断结果的统一评估和比较变得困难。来自 10 个欧洲国家的主要实验室在欧洲资助的 EuroChimerism Concerted Action 合作研究中进行了合作,目的是开发一种标准化的诊断方法,用于检测和监测接受同种异体干细胞移植的患者的嵌合体。在对一大组微卫星/短串联重复(STR)基因座进行广泛分析后,建立了包含 13 个 STR 标记的 EuroChimerism(EUC)面板,旨在最佳满足定量嵌合体分析的特定要求。基于高度严格的选择标准,EUC 面板在任何移植环境中都提供多个信息标记。标准化的 STR-PCR 检测可在 0.8%至 1.6%的灵敏度范围内检测到供体或受体来源的细胞。此外,EUC 检测法有助于对供体和受体造血细胞进行准确和可重复的定量。广泛使用欧洲协调的嵌合体分析协议将为最佳诊断支持和及时治疗决策提供基础。