Harnessing natural killer cells for the treatment of multiple myeloma

被引:19
|
作者
Clara, Joseph A. [1 ]
Childs, Richard W. [1 ]
机构
[1] NHLBI, NIH, 10 Ctr Dr, Bethesda, MD 20892 USA
关键词
Multiple myeloma; NK cells; Immunotherapy; Elotuzumab; Daratumumab; BCMA CAR; CAR NK; mbIL-21 feeder cells; LENALIDOMIDE PLUS DEXAMETHASONE; DEPENDENT CELLULAR CYTOTOXICITY; KIR ANTIBODY IPH2101; REGULATORY T-CELLS; TGF-BETA RECEPTOR; MONOCLONAL-ANTIBODY; NK CELLS; IN-VIVO; BONE-MARROW; MEDIATED LYSIS;
D O I
10.1053/j.seminoncol.2022.01.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Multiple myeloma (MM) is hematologic malignancy that is associated with profound immune alterations. Myeloma cells are susceptible to killing by natural killer (NK) cells but acquire the ability to elude NK cell surveillance by avoiding recognition and suppressing NK cell function. Major advances in the treatment of multiple myeloma have been achieved by effective new drugs that redirect NK cells and enhance their function. Despite significant progress, myeloma remains incurable and novel treatment approaches are required. Strategies to take advantage of the intrinsic antitumor properties of NK cells to treat MM represent a novel immunotherapeutic approach. One such strategy is adoptive NK cell therapy that consist of infusions of NK cells that have been propagated ex vivo. Adoptive NK cell therapy encompasses contemporary genetic engineering strategies such as chimeric antigen receptor (CAR)-engineered NK cells. An alternative approach involves the use of pharmacologic agents to enhance NK cell activity against myeloma. NK cell-modulating therapies can be used to bolster the function of endogenous NK cells or to enhance the efficacy of adoptively infused NK cells. Here, we review the mechanistic complexities influencing NK cell activity in MM and highlight a variety of innovative NK cell-based strategies being developed for the treatment of MM. Published by Elsevier Inc.
引用
收藏
页码:69 / 85
页数:17
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