← 返回前沿论文

新一代 CAR-NK 免疫疗法的工程化改造

英文原题:Engineering the next generation of CAR-NK immunotherapies.

PubMed 2021/08/28(内容时间) Int J Hematol Q3 · IF 1.9(JCR 2025)

研究概要

在过去几年中,细胞免疫治疗已成为某些形式血液恶性肿瘤的新型治疗选择,多种CAR-T疗法现已在临床上常规应用。

中文摘要

在过去几年中,细胞免疫治疗已成为某些形式血液系统恶性肿瘤的新型治疗选择,多种CAR-T疗法现已在临床中常规应用。自体细胞产品生产的局限性以及CAR-T细胞毒性的挑战,凸显了开发通用、安全且强效的新型细胞治疗产品的必要性。自然杀伤(NK)细胞是先天免疫系统的一部分,具有独特优势,包括作为现货型疗法的潜力。最近一项在复发/难治性淋巴系统恶性肿瘤患者中进行的CD19-CAR-NK输注的首次人体试验证明其安全性良好,并显示出有前景的临床活性。基于这些令人鼓舞的临床反应,研究目前正在积极探索通过延长体内持久性和克服功能性耗竭机制来进一步增强CAR-NK细胞效力的方法。除了这些调节CAR-NK细胞内在特性的策略外,越来越多的努力正在将血液系统恶性肿瘤中取得的成功转化到实体瘤领域。本综述将概述当前趋势和不断发展的概念,以通过基因工程改造下一代CAR-NK疗法。重点将放在创新的多重工程化方法上,包括CRISPR/Cas9,以克服CAR-NK功能性耗竭并重编程免疫细胞代谢以增强效力。

展开英文摘要原文

Over the past few years, cellular immunotherapy has emerged as a novel treatment option for certain forms of hematologic malignancies with multiple CAR-T therapies now routinely administered in the clinic. The limitations of generating an autologous cell product and the challenges of toxicity with CAR-T cells underscore the need to develop novel cell therapy products that are universal, safe, and potent. Natural killer (NK) cells are part of the innate immune system with unique advantages, including the potential for off-the-shelf therapy. A recent first-in-human trial of CD19-CAR-NK infusion in patients with relapsed/refractory lymphoid malignancies proved safe with promising clinical activity. Building on these encouraging clinical responses, research is now actively exploring ways to further enhance CAR-NK cell potency by prolonging in vivo persistence and overcoming mechanisms of functional exhaustion. Besides these strategies to modulate CAR-NK cell intrinsic properties, there are increasing efforts to translate the successes seen in hematologic malignancies to the solid tumor space. This review will provide an overview on current trends and evolving concepts to genetically engineer the next generation of CAR-NK therapies. Emphasis will be placed on innovative multiplexed engineering approaches including CRISPR/Cas9 to overcome CAR-NK functional exhaustion and reprogram immune cell metabolism for enhanced potency.

论文信息

作者
Biederstädt A、Rezvani K
第一作者单位
Department of Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd., Unit 423, Houston, TX, USA.United States
通讯作者单位
Department of Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd., Unit 423, Houston, TX, USA. krezvani@mdanderson.org.United States
文献类型
综述
期刊
International journal of hematology2021 Nov
原文标识
PubMed 34453686 · DOI 10.1007/s12185-021-03209-4