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靶向免疫治疗:利用免疫系统对抗多发性骨髓瘤

英文原题:Targeted immunotherapy: harnessing the immune system to battle multiple myeloma.

PubMed 2024/01/27(内容时间) Cell Death Discov Q1 · IF 10.4(JCR 2025)

研究概要

多发性骨髓瘤(MM)仍然是一种无法治愈的血液系统恶性肿瘤,其特征是患者免疫系统的进行性功能障碍。

中文摘要

多发性骨髓瘤(MM)仍然是一种无法治愈的血液系统恶性肿瘤,其特征是患者免疫系统进行性功能障碍。在此背景下,近年来MM的免疫治疗已成为一个突出的研究领域。针对MM已开发了多种靶向免疫治疗策略,如单克隆抗体、抗体药物偶联物、双特异性抗体、CAR-T 细胞/自然杀伤(NK)细胞以及检查点抑制剂。本综述旨在讨论这些免疫治疗有前景的实验和临床证据及其作用机制。具体而言,我们将探讨基于外泌体的双特异性单克隆抗体的设计,其提供了无细胞免疫治疗选择。随着众多新兴免疫治疗的发展,骨髓瘤的治疗格局持续演变。鉴于这些方法在通过免疫靶向治疗调节MM免疫环境方面具有显著优势,它们为选择MM的前沿治疗提供了新的视角。

展开英文摘要原文

Multiple myeloma (MM) remains an incurable hematological malignancy disease characterized by the progressive dysfunction of the patient's immune system. In this context, immunotherapy for MM has emerged as a prominent area of research in recent years. Various targeted immunotherapy strategies, such as monoclonal antibodies, antibody-drug conjugates, bispecific antibodies, chimeric antigen receptor T cells/natural killer (NK) cells, and checkpoint inhibitors have been developed for MM. This review aims to discuss promising experimental and clinical evidence as well as the mechanisms of action underlying these immunotherapies. Specifically, we will explore the design of exosome-based bispecific monoclonal antibodies that offer cell-free immunotherapy options. The treatment landscape for myeloma continues to evolve with the development of numerous emerging immunotherapies. Given their significant advantages in modulating the MM immune environment through immune-targeted therapy, these approaches provide novel perspectives in selecting cutting-edge treatments for MM.

论文信息

作者
Xu L、Wen C、Xia J、Zhang H、Liang Y、Xu X
第一作者单位
Department of Hematology, Affiliated Hospital of Jining Medical University, Jining Medical University, Jining, 272029, Shandong, China.China
通讯作者单位
Affiliated Hospital of Jining Medical University, Jining Medical University, Jining, 272029, Shandong, China. xiaoxu.med@gmail.com.China
文献类型
综述
期刊
Cell death discovery2024 Jan 27
原文标识
PubMed 38280847 · DOI 10.1038/s41420-024-01818-6