Suppr超能文献

工程化下一代 CAR-NK 免疫疗法。

Engineering the next generation of CAR-NK immunotherapies.

机构信息

Department of Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd., Unit 423, Houston, TX, USA.

Department of Medicine III, Hematology/Oncology, Klinikum rechts der Isar, Technical University of Munich, Ismaninger Str. 22, 81675, Munich, Germany.

出版信息

Int J Hematol. 2021 Nov;114(5):554-571. doi: 10.1007/s12185-021-03209-4. Epub 2021 Aug 28.

Abstract

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.

摘要

在过去的几年中,细胞免疫疗法已经成为某些血液系统恶性肿瘤的一种新的治疗选择,目前临床上已经常规应用了多种 CAR-T 疗法。由于自体细胞产品的生成受限以及 CAR-T 细胞的毒性问题,因此需要开发通用、安全且有效的新型细胞治疗产品。自然杀伤 (NK) 细胞是先天免疫系统的一部分,具有独特的优势,包括潜在的现货治疗能力。最近在复发/难治性淋巴恶性肿瘤患者中进行的 CD19-CAR-NK 输注的首次人体试验证明是安全的,且具有有前景的临床活性。在这些令人鼓舞的临床反应的基础上,目前的研究正在积极探索通过延长体内持久性和克服功能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,人们越来越努力地将在血液系统恶性肿瘤中取得的成功转化为实体肿瘤领域。这篇综述将概述当前的趋势和不断发展的概念,以对下一代 CAR-NK 疗法进行基因工程改造。重点将放在创新的多重工程方法上,包括 CRISPR/Cas9,以克服 CAR-NK 功能耗竭并重新编程免疫细胞代谢以增强效力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f51/8397867/9437d83ea421/12185_2021_3209_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验