Linke B, Pyttlich J, Tiemann M, Suttorp M, Parwaresch R, Hiddemann W, Kneba M
Department of Internal Medicine, Georg-August University, Goettingen, Germany.
Leukemia. 1995 May;9(5):840-7.
The third complementarity determining region (CDR3) of the hypervariable domain of immunoglobulin heavy chain (IgH) genes represents a highly variable and clone-specific IgH-CDR3 sequences in 10 non-Hodgkin's lymphomas (NHL), five chronic lymphocytic leukemias (CLL) and five acute lymphoblastic leukemias (ALL) of B cell lineage. The IgH-CDR3 sequences were amplified using DNA extracted from clinical specimens (bone marrow, peripheral blood and fresh-frozen or paraffin-embedded lymph nodes) by a semi-nested PCR with consensus primers directed to conserved regions within the variable (VH) and the joining (JH) gene segments. In 17/20 samples (85%), a distinct IgH-CDR3 PCR product was obtained. Individual PCR products were sequenced after cloning. The nucleotide sequences of 134 randomly chosen recombinant vectors were determined demonstrating in 17/20 cases (85%) monoclonal VH-N-DH-N-JH junctions. Analysis of PCR products by temperature-gradient gel electrophoresis (TGGE) confirmed the specificity of the IgH-CDR3 PCR/sequencing results. Moreover, the combination of PCR/TGGE technology allowed the rapid and specific characterization of clonal IgH-CDR3 junctions in B cell proliferations by direct sequencing even in the presence of admixed polyclonal B cells.
免疫球蛋白重链(IgH)基因高变区的第三个互补决定区(CDR3)代表了B细胞系10例非霍奇金淋巴瘤(NHL)、5例慢性淋巴细胞白血病(CLL)和5例急性淋巴细胞白血病(ALL)中高度可变且具有克隆特异性的IgH - CDR3序列。使用从临床标本(骨髓、外周血以及新鲜冷冻或石蜡包埋的淋巴结)中提取的DNA,通过半巢式PCR扩增IgH - CDR3序列,该PCR使用针对可变区(VH)和连接区(JH)基因片段内保守区域的共有引物。在20个样本中的17个(85%)获得了独特的IgH - CDR3 PCR产物。克隆后对各个PCR产物进行测序。测定了134个随机选择的重组载体的核苷酸序列,在20例中的17例(85%)显示出单克隆VH - N - DH - N - JH连接。通过温度梯度凝胶电泳(TGGE)分析PCR产物证实了IgH - CDR3 PCR/测序结果的特异性。此外,PCR/TGGE技术的联合应用即使在存在混合多克隆B细胞的情况下,也能通过直接测序快速且特异地鉴定B细胞增殖中克隆性IgH - CDR3连接。