Bi-specific and Tri-specific NK Cell Engagers: The New Avenue of Targeted NK Cell Immunotherapy

被引:42
作者
Phung, Shee Kwan [1 ]
Miller, Jeffrey S. [1 ]
Felices, Martin [1 ]
机构
[1] Univ Minnesota, Dept Med, Div Hematol Oncol & Transplantat, Box 736 UMHC, Minneapolis, MN 55455 USA
关键词
NATURAL-KILLER-CELLS; IN-VIVO EXPANSION; INHIBITORY RECEPTORS; ADOPTIVE TRANSFER; ANTIBODY IPH2101; BREAST-CANCER; PHASE-1; TRIAL; T-CELLS; CYTOKINE; CYTOTOXICITY;
D O I
10.1007/s40291-021-00550-6
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Natural killer (NK) cell-mediated cancer immunotherapy has grown significantly over the past two decades. More recently, multi-specific engagers have been developed as cancer therapeutics to effectively arm endogenous NK cells to more potently induce specific cytolytic responses against tumor targets. This review explores the bi- and tri-specific NK/tumor engagers that are emerging as a new generation of immunotherapeutics. These molecules vary in configuration, but they typically have small molecular weights and domains that engage specific tumor antigens and NK cell-activating receptors such as CD16, NKp30, NKp46, and NKG2D. They have demonstrated compelling potential in boosting NK cell cytotoxicity against specific tumor targets. This highly adaptable off-the-shelf platform, which in some formats also integrates cytokines, is poised to revolutionize targeted NK cell immunotherapy, either as a monotherapy or in combination with other effective anti-cancer therapies.
引用
收藏
页码:577 / 592
页数:16
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