Human Oncology and Pathogenesis Program, Molecular Cancer Medicine Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Louis V. Gerstner Jr. Graduate School of Biomedical Sciences, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Sci Adv. 2023 Sep 22;9(38):eadg0488. doi: 10.1126/sciadv.adg0488. Epub 2023 Sep 20.
Measurable residual disease (MRD), defined as the population of cancer cells that persist following therapy, serves as the critical reservoir for disease relapse in acute myeloid leukemia and other malignancies. Understanding the biology enabling MRD clones to resist therapy is necessary to guide the development of more effective curative treatments. Discriminating between residual leukemic clones, preleukemic clones, and normal precursors remains a challenge with current MRD tools. Here, we developed a single-cell MRD (scMRD) assay by combining flow cytometric enrichment of the targeted precursor/blast population with integrated single-cell DNA sequencing and immunophenotyping. Our scMRD assay shows high sensitivity of approximately 0.01%, deconvolutes clonal architecture, and provides clone-specific immunophenotypic data. In summary, our scMRD assay enhances MRD detection and simultaneously illuminates the clonal architecture of clonal hematopoiesis/preleukemic and leukemic cells surviving acute myeloid leukemia therapy.
可测量残留疾病(MRD)定义为治疗后持续存在的癌细胞群体,是急性髓系白血病和其他恶性肿瘤疾病复发的关键储存库。了解使 MRD 克隆能够抵抗治疗的生物学特性,对于指导更有效的治愈性治疗的发展是必要的。用当前的 MRD 工具区分残留白血病克隆、前白血病克隆和正常前体仍然是一个挑战。在这里,我们通过结合靶向前体细胞/母细胞群体的流式细胞术富集与整合的单细胞 DNA 测序和免疫表型分析,开发了一种单细胞 MRD(scMRD)检测方法。我们的 scMRD 检测方法具有约 0.01%的高灵敏度,可推断克隆结构,并提供克隆特异性免疫表型数据。总之,我们的 scMRD 检测方法增强了 MRD 的检测,并同时阐明了急性髓系白血病治疗后存活的克隆性造血/前白血病和白血病细胞的克隆结构。