Ishibashi Mariko
Department of Microbiology and Immunology, Nippon Medical School.
Rinsho Ketsueki. 2024;65(9):1058-1065. doi: 10.11406/rinketsu.65.1058.
Multiple myeloma (MM) is currently treated with combined immunotherapies targeting the immune microenvironment surrounding MM cells. Although novel immunotherapeutic agents for MM have improved complete response rates and survival time, some patients experience repeated relapses and die of MM because its progression is strongly influenced by the immune microenvironment as well as cytogenetic abnormalities of MM cells. Various studies have elucidated the mechanisms underlying the immunosuppressive immune microenvironment of MM. Recently, single-cell RNA sequencing and cytometry by time-of-flight analysis have revealed spatiotemporal crosstalk between MM and immune cells in the bone marrow of patients with MM. These studies showed that immunosuppression appears in the early stages of MM and becomes stronger as the disease progresses, leading to immunotherapy resistance. Understanding the state of the immune microenvironment in patients with MM is important for developing immunotherapeutic strategies for long-term complete response and cure.
多发性骨髓瘤(MM)目前采用针对MM细胞周围免疫微环境的联合免疫疗法进行治疗。尽管用于MM的新型免疫治疗药物提高了完全缓解率和生存时间,但一些患者仍会反复复发并死于MM,因为其进展受到免疫微环境以及MM细胞细胞遗传学异常的强烈影响。各种研究已经阐明了MM免疫抑制性免疫微环境的潜在机制。最近,单细胞RNA测序和飞行时间分析流式细胞术揭示了MM患者骨髓中MM与免疫细胞之间的时空串扰。这些研究表明,免疫抑制在MM的早期阶段出现,并随着疾病进展而增强,导致免疫治疗耐药。了解MM患者的免疫微环境状态对于制定实现长期完全缓解和治愈的免疫治疗策略很重要。