Deane M, McCarthy K P, Wiedemann L M, Norton J D
Department of Haematology, Royal Free Hospital, London, UK.
Leukemia. 1991 Aug;5(8):726-30.
Several groups have recently described methods for the detection of clonal immunoglobulin heavy chain (IgH) gene rearrangements in B-cell malignancies by polymerase chain reaction (PCR) gene amplification using variable region-(VH) and joining (JH) region-specific primers. The simplest methods utilize a single VH primer specific for sequences present in most VH regions corresponding to the third framework region (FR3). An alternative approach is to use a panel of VH family-specific primers specific for the first framework regions (FR1). In the course of nucleotide sequence analysis of IgH gene rearrangements amplified using a VH FR1 primer panel, these authors previously observed 3' VH region deletion and/or base mis-matches sufficient to prevent efficient priming from the VH FR3 primer target sequence in a significant minority of cases of B-lineage malignancy. An improved PCR method has therefore been developed by using a panel of seven VH FR1 family-specific primers incorporated in a single reaction. By using this method clonal IgH gene rearrangement is detected in 15 of 16 cases of B-lineage malignancy. Significantly, this series included four cases of B-lymphoma in which previous attempts to detect PCR clonal IgH gene rearrangements using a VH FR3 primer were unsuccessful. In two of these cases, nucleotide sequence analysis of the amplified DNA showed that failure to prime with the VH FR3 primer was likely to be attributable to insufficient homology with the target sequence. The use of the approach described in this paper should significantly improve the reliability of detection of B-lymphoid clonality by PCR.
最近有几个研究小组描述了通过聚合酶链反应(PCR)基因扩增,使用可变区(VH)和连接区(JH)特异性引物来检测B细胞恶性肿瘤中克隆性免疫球蛋白重链(IgH)基因重排的方法。最简单的方法是使用一种针对大多数VH区域中与第三框架区(FR3)相对应序列的单一VH引物。另一种方法是使用一组针对第一框架区(FR1)的VH家族特异性引物。在使用VH FR1引物组扩增的IgH基因重排的核苷酸序列分析过程中,这些作者之前观察到,在相当一部分B系恶性肿瘤病例中,3' VH区域缺失和/或碱基错配足以阻止从VH FR3引物靶序列进行有效引物延伸。因此,通过在单个反应中使用一组七种VH FR1家族特异性引物,开发了一种改进的PCR方法。使用这种方法,在16例B系恶性肿瘤病例中的15例中检测到了克隆性IgH基因重排。值得注意的是,该系列包括4例B淋巴瘤病例,之前使用VH FR3引物检测PCR克隆性IgH基因重排的尝试均未成功。在其中2例病例中,对扩增DNA的核苷酸序列分析表明,未能用VH FR3引物进行引物延伸可能归因于与靶序列的同源性不足。本文所述方法的使用应能显著提高通过PCR检测B淋巴细胞克隆性的可靠性。