Draube A, Pfister R, Vockerodt M, Schuster S, Kube D, Diehl V, Tesch H
Department of Internal Medicine I, University of Cologne, 50924 Cologne, Germany.
Ann Hematol. 2001 Feb;80(2):83-9. doi: 10.1007/s002770000245.
In multiple myeloma, the polymerase chain reaction (PCR) of the Ig heavy chain with allele-specific oligonucleotide (ASO) primers is a common and well-described method of identifying the tumor clone in peripheral blood (PB), bone marrow (BM) or leukapheresis products (LA). A factor which is crucial to the detection of clonal Ig rearrangements lies in the 'purity' of the tumor tissue used for the consensus PCR. We describe the application of a method to enrich CD138 positive myeloma cells derived from weakly infiltrated PB-, BM- and LA-samples. These are subjected to immunomagnetic enrichment with the MACS system, using an CD138 antibody directly conjugated to magnetic beads to obtain an enriched tumor cell population and the subsequent amplification of tumor specific IgH rearrangements. We investigated 29 samples (ten PB, ten BM, nine LA) with a median myeloma cell content of 0.5%. The approach led to a median enrichment factor of 118. Tumor-specific rearrangements could be amplified reproducibly from samples containing less than 0.1% myeloma cells.
在多发性骨髓瘤中,使用等位基因特异性寡核苷酸(ASO)引物对免疫球蛋白重链进行聚合酶链反应(PCR)是一种常见且已被充分描述的方法,用于在外周血(PB)、骨髓(BM)或白细胞分离产物(LA)中鉴定肿瘤克隆。检测克隆性免疫球蛋白重排的一个关键因素在于用于一致性PCR的肿瘤组织的“纯度”。我们描述了一种方法的应用,该方法用于富集源自轻度浸润的PB、BM和LA样本的CD138阳性骨髓瘤细胞。使用直接与磁珠偶联的CD138抗体,通过MACS系统对这些细胞进行免疫磁珠富集,以获得富集的肿瘤细胞群体,并随后扩增肿瘤特异性免疫球蛋白重链(IgH)重排。我们研究了29个样本(10个PB样本、10个BM样本、9个LA样本),骨髓瘤细胞含量中位数为0.5%。该方法使富集倍数中位数达到118。从骨髓瘤细胞含量低于0.1%的样本中可重复扩增出肿瘤特异性重排。