Targeting KIR as a novel approach to improve CAR-NK cell function

Lara V. Graham, J. G. Fisher, S. Khakoo, Matthew D. Blunt
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Abstract

Chimeric antigen receptor (CAR) NK cells are demonstrating promising activity in clinical trials and possess a favorable safety profile compared to CAR-T cells. The Killer cell Immunoglobulin-like Receptors (KIR) have a critical role in the control of NK cell function, and recently, this family of activating and inhibitory receptors have been targeted to improve CAR-NK function. These strategies include the utilisation of inhibitory KIR to reduce trogocytosis-associated NK cell fratricide, the downregulation of inhibitory KIR on CAR-NK cells to alleviate HLA mediated suppression, the selection of CAR-NK cell donors enriched for activating KIR, and the use of activating KIR intracellular domains within novel CAR constructs. These pre-clinical studies demonstrate the potential utility of targeting the KIR to improve CAR-NK cell efficacy and patient outcomes.
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将 KIR 作为改善 CAR-NK 细胞功能的新方法
嵌合抗原受体(CAR) NK细胞在临床试验中显示出有希望的活性,与CAR- t细胞相比,具有良好的安全性。杀伤细胞免疫球蛋白样受体(Killer cell Immunoglobulin-like Receptors, KIR)在控制NK细胞功能中起着至关重要的作用,最近,这一激活和抑制受体家族已经成为改善CAR-NK功能的目标。这些策略包括利用抑制性KIR来减少与巨噬细胞病相关的NK细胞自相残杀,下调CAR-NK细胞上的抑制性KIR以减轻HLA介导的抑制,选择富集激活KIR的CAR-NK细胞供体,以及在新型CAR构建中使用激活KIR的细胞内结构域。这些临床前研究证明了靶向KIR改善CAR-NK细胞疗效和患者预后的潜在效用。
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