Droese J, Langerak A W, Groenen P J T A, Brüggemann M, Neumann P, Wolvers-Tettero I L M, van Altena M C, Kneba M, van Dongen J J M
Medical Clinic II, University of Kiel, Germany.
Leukemia. 2004 Sep;18(9):1531-8. doi: 10.1038/sj.leu.2403428.
The BIOMED-2 Concerted Action BMH4-CT98-3936 on 'Polymerase chain reaction (PCR)-based clonality studies for early diagnosis of lymphoproliferative disorders' developed standardized PCR protocols for detection of immunoglobulin (Ig) and T-cell receptor (TCR) rearrangements, including TCR beta (TCRB). As no comparable TCRB PCR method pre-existed and only a limited number of samples was tested within the BIOMED-2 study, we initiated this study for further validation of the newly developed TCRB PCR approach by comparing PCR data with previously generated Southern blot (SB) data in a series of 66 immature (ALL) and 36 mature T-cell malignancies. In 91% of cases, concordant PCR and SB results were found. Discrepancies consisted of either failure to detect SB-detected TCRB rearrangements by PCR (6.5%) or detection of an additional non-SB defined rearrangement (2.5%). In 99% of cases (99/100), at least one clonal TCRB rearrangement was detected by PCR in the SB-positive cases. A predominance of complete Vbeta-Jbeta rearrangements was seen in TCRalphabeta(+) T-cell malignancies and CD3-negative T-ALL (100 and 90%, respectively), whereas in TCRgammadelta(+) T-ALL, more incomplete Dbeta-Jbeta TCRB rearrangements were detected (73%). Our results underline the reliability of this new TCRB PCR method and its strategic applicability in clonality diagnostics of lymphoproliferative disorders and MRD studies.
“基于聚合酶链反应(PCR)的克隆性研究用于淋巴增殖性疾病的早期诊断”这一BIOMED-2联合行动项目BMH4-CT98-3936,开发了用于检测免疫球蛋白(Ig)和T细胞受体(TCR)重排的标准化PCR方案,包括TCRβ(TCRB)。由于此前不存在可比的TCRB PCR方法,且在BIOMED-2研究中仅测试了有限数量的样本,我们启动了本研究,通过将PCR数据与先前在一系列66例未成熟(急性淋巴细胞白血病,ALL)和36例成熟T细胞恶性肿瘤中生成的Southern印迹(SB)数据进行比较,进一步验证新开发的TCRB PCR方法。在91%的病例中,发现PCR和SB结果一致。差异包括PCR未能检测到SB检测到的TCRB重排(6.5%)或检测到额外的非SB定义的重排(2.5%)。在99%的病例(99/100)中,SB阳性病例通过PCR检测到至少一种克隆性TCRB重排。在TCRαβ(+)T细胞恶性肿瘤和CD3阴性T-ALL中分别有100%和90%出现了主要的完整Vβ-Jβ重排,而在TCRγδ(+)T-ALL中,检测到更多不完整的Dβ-Jβ TCRB重排(73%)。我们的结果强调了这种新的TCRB PCR方法的可靠性及其在淋巴增殖性疾病克隆性诊断和微小残留病(MRD)研究中的战略适用性。