Division of Hematology-Oncology-Stem Cell Transplantation and Cancer Biology, Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA.
Blood. 2012 Nov 22;120(22):4407-17. doi: 10.1182/blood-2012-05-429811. Epub 2012 Aug 28.
The ability to distinguish clonal B-cell populations based on the sequence of their rearranged immunoglobulin heavy chain (IgH) locus is an important tool for diagnosing B-cell neoplasms and monitoring treatment response. Leukemic precursor B cells may continue to undergo recombination of the IgH gene after malignant transformation; however, the magnitude of evolution at the IgH locus is currently unknown. We used next-generation sequencing to characterize the repertoire of IgH sequences in diagnostic samples of 51 children with B precursor acute lymphoblastic leukemia (B-ALL). We identified clonal IgH rearrangements in 43 of 51 (84%) cases and found that the number of evolved IgH sequences per patient ranged dramatically from 0 to 4024. We demonstrate that the evolved IgH sequences are not the result of amplification artifacts and are unique to leukemic precursor B cells. In addition, the evolution often follows an allelic exclusion pattern, where only 1 of 2 rearranged IgH loci exhibit ongoing recombination. Thus, precursor B-cell leukemias maintain evolution at the IgH locus at levels that were previously underappreciated. This finding sheds light on the mechanisms associated with leukemic clonal evolution and may fundamentally change approaches for monitoring minimal residual disease burden.
基于重排免疫球蛋白重链(IgH)基因序列来区分克隆性 B 细胞群体,是诊断 B 细胞肿瘤和监测治疗反应的重要工具。白血病前体 B 细胞在恶性转化后可能继续进行 IgH 基因的重组;然而,目前尚不清楚 IgH 基因座的进化程度。我们使用下一代测序技术,对 51 例 B 前体急性淋巴细胞白血病(B-ALL)患儿的诊断样本中的 IgH 序列库进行了特征分析。我们在 51 例中的 43 例(84%)中鉴定出克隆性 IgH 重排,并且发现每位患者的进化 IgH 序列数量从 0 到 4024 不等,变化范围很大。我们证明,进化的 IgH 序列不是扩增假象的结果,而是白血病前体 B 细胞所特有的。此外,这种进化通常遵循等位基因排斥模式,即只有 2 个重排的 IgH 基因座中的 1 个存在持续的重组。因此,前体 B 细胞白血病在 IgH 基因座上保持着以前未被充分认识的进化水平。这一发现揭示了与白血病克隆进化相关的机制,并可能从根本上改变监测微小残留病负担的方法。