Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Harvard Medical School, Boston, MA, USA.
Nat Cancer. 2020 May;1(5):493-506. doi: 10.1038/s43018-020-0053-3. Epub 2020 Apr 27.
Precursor states of Multiple Myeloma (MM) and its native tumor microenvironment need in-depth molecular characterization to better stratify and treat patients at risk. Using single-cell RNA sequencing of bone marrow cells from precursor stages, MGUS and smoldering myeloma (SMM), to full-blown MM alongside healthy donors, we demonstrate early immune changes during patient progression. We find NK cell abundance is frequently increased in early stages, and associated with altered chemokine receptor expression. As early as SMM, we show loss of GrK memory cytotoxic T-cells, and show their critical role in MM immunosurveillance in mouse models. Finally, we report MHC class II dysregulation in CD14 monocytes, which results in T cell suppression . These results provide a comprehensive map of immune changes at play over the evolution of pre-malignant MM, which will help develop strategies for immune-based patient stratification.
多发性骨髓瘤(MM)前体状态及其固有肿瘤微环境需要深入的分子特征分析,以便更好地对处于危险中的患者进行分层和治疗。我们利用骨髓细胞的单细胞 RNA 测序,对前驱阶段、MGUS 和冒烟型骨髓瘤(SMM),以及进展为完全 MM 的患者以及健康供体进行研究,在患者进展过程中展示了早期的免疫变化。我们发现 NK 细胞丰度在早期阶段经常增加,并与改变的趋化因子受体表达相关。早在 SMM 阶段,我们就发现 GrK 记忆细胞毒性 T 细胞缺失,并在小鼠模型中显示其在 MM 免疫监视中的关键作用。最后,我们报告了 CD14 单核细胞中 MHC Ⅱ类的失调,这导致了 T 细胞抑制。这些结果提供了恶性前 MM 演变过程中免疫变化的综合图谱,这将有助于制定基于免疫的患者分层策略。