Moscvin Maria, Evans Benjamin, Bianchi Giada
Department of Medicine, Division of Hematology, Brigham and Womens Hospital, Boston, MA 02115, USA.
Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
J Cancer Metastasis Treat. 2023;9. doi: 10.20517/2394-4722.2022.110. Epub 2023 May 16.
Multiple myeloma (MM) is a disease of clonally differentiated plasma cells. MM is almost always preceded by precursor conditions, monoclonal gammopathy of unknown significance (MGUS), and smoldering MM (SMM) through largely unknown molecular events. Genetic alterations of the malignant plasma cells play a critical role in patient clinical outcomes. Del(17p), t(4;14), and additional chromosomal alterations such as del(1p32), gain(1q) and MYC translocations are involved in active MM evolution. Interestingly, these genetic alterations appear strikingly similar in transformed plasma cell (PC) clones from MGUS, SMM, and MM stages. Recent studies show that effectors of the innate and adaptive immune response show marked dysfunction and skewing towards a tolerant environment that favors disease progression. The MM myeloid compartment is characterized by myeloid-derived suppressor cells (MDSCs), dendritic cells as well as M2-like phenotype macrophages that promote immune evasion. Major deregulations are found in the lymphoid compartment as well, with skewing towards immune tolerant Th17 and Treg and inhibition of CD8+ cytotoxic and CD4+ activated effector T cells. In summary, this review will provide an overview of the complex cross-talk between MM plasma cells and immune cells in the microenvironment and the molecular mechanisms promoting progression from precursor states to full-blown myeloma.
多发性骨髓瘤(MM)是一种克隆性分化浆细胞疾病。MM几乎总是由前驱疾病,即意义未明的单克隆丙种球蛋白病(MGUS)和冒烟型MM(SMM)发展而来,其分子机制大多不明。恶性浆细胞的基因改变在患者临床结局中起关键作用。17号染色体短臂缺失(Del(17p))、4号和14号染色体易位(t(4;14))以及其他染色体改变,如1号染色体短臂32区缺失(del(1p32))、1号染色体长臂增加(gain(1q))和MYC易位,都参与了活动性MM的进展。有趣的是,这些基因改变在MGUS、SMM和MM阶段转化的浆细胞(PC)克隆中惊人地相似。最近的研究表明,先天性和适应性免疫反应的效应器表现出明显的功能障碍,并倾向于向有利于疾病进展的耐受环境倾斜。MM髓系区室的特征是髓系来源的抑制细胞(MDSC)、树突状细胞以及促进免疫逃逸的M2样表型巨噬细胞。在淋巴区室也发现了主要的失调,倾向于免疫耐受的Th17和调节性T细胞(Treg),并抑制CD8 + 细胞毒性T细胞和CD4 + 活化效应T细胞。总之,本综述将概述MM浆细胞与微环境中免疫细胞之间复杂的相互作用,以及促进从前驱状态发展为成熟骨髓瘤的分子机制。