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挖掘 NK 细胞免疫治疗多发性骨髓瘤的潜力

英文原题:Harnessing the Potential of NK Cell-Based Immunotherapies against Multiple Myeloma.

查看英文原题

Harnessing the Potential of NK Cell-Based Immunotherapies against Multiple Myeloma.

PubMed 2022/01/24(内容时间) Cells Q2 · IF 6(JCR 2025)

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中文摘要

自然杀伤(NK)细胞疗法因其作为细胞溶解效应器的效力以及与同时进行的治疗的协同作用,已成为有前景的抗癌治疗方法。多发性骨髓瘤(MM)是一种侵袭性B细胞恶性肿瘤,尽管新型治疗药物不断开发,但仍无法治愈且复发率高。在MM中,不利的肿瘤微环境阻止宿主NK细胞发挥其细胞溶解功能。NK细胞免疫疗法的发展致力于克服这种改变的免疫格局,并可根据细胞来源分为两大类:自体或异体。在这篇综述中,我们比较了每组中的治疗方法,如自体嵌合抗原受体(CAR)NK细胞和异体现货型NK细胞输注,以及它们与现有MM疗法(包括单克隆抗体和蛋白酶体抑制剂)的联合效果。我们还根据每位患者的免疫特征讨论了它们在临床治疗方案中的定位。通过这一探讨,我们希望确切发现每种基于NK细胞的治疗何时能为MM患者产生最大获益。

展开英文摘要原文

Natural killer (NK) cell-based therapies have emerged as promising anticancer treatments due to their potency as cytolytic effectors and synergy with concurrent treatments. Multiple myeloma (MM) is an aggressive B-cell malignancy that, despite development of novel therapeutic agents, remains incurable with a high rate of relapse. In MM, the inhospitable tumor microenvironment prevents host NK cells from exerting their cytolytic function.

The development of NK cell immunotherapy works to overcome this altered immune landscape and can be classified in two major groups based on the origin of the cell: autologous or allogeneic. In this review, we compare the treatments in each group, such as autologous chimeric antigen receptor (CAR) NKs and allogeneic off-the-shelf NK cell infusions, and their combinatorial effect with existing MM therapies including monoclonal antibodies and proteasome inhibitors.

We also discuss their placement in clinical treatment regimens based on the immune profile of each patient. Through this examination, we would like to discover precisely when each NK cell-based treatment will produce the maximum benefit to the MM patient.

论文信息

作者
Reina-Ortiz C、Giraldos D、Azaceta G、Palomera L、Marzo I、Naval J、Villalba M、Anel A
单位
Apoptosis, Immunity & Cancer Group, Department Biochemistry and Molecular and Cell Biology, Faculty of Sciences, University of Zaragoza and Aragón Health Research Institute (IIS Aragón), 50009 Zaragoza, Spain.Spain
文献类型
非美国政府资助研究 · 综述
期刊
Cells2022 Jan 24
原文标识
PubMed 35159200 · DOI 10.3390/cells11030392