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嵌合抗原受体自然杀伤(CAR-NK)细胞疗法的进展:从嵌合抗原受体 T(CAR-T)细胞疗法中吸取的经验教训。

Advancements in CAR-NK therapy: lessons to be learned from CAR-T therapy.

机构信息

Cancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, Canada.

Department of Medicine, University of Ottawa, Ottawa, Canada.

出版信息

Front Immunol. 2023 May 2;14:1166038. doi: 10.3389/fimmu.2023.1166038. eCollection 2023.

DOI:10.3389/fimmu.2023.1166038
PMID:37205115
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10187144/
Abstract

Advancements in chimeric antigen receptor engineered T-cell (CAR-T) therapy have revolutionized treatment for several cancer types over the past decade. Despite this success, obstacles including the high price tag, manufacturing complexity, and treatment-associated toxicities have limited the broad application of this therapy. Chimeric antigen receptor engineered natural killer cell (CAR-NK) therapy offers a potential opportunity for a simpler and more affordable "off-the-shelf" treatment, likely with fewer toxicities. Unlike CAR-T, CAR-NK therapies are still in early development, with few clinical trials yet reported. Given the challenges experienced through the development of CAR-T therapies, this review explores what lessons we can apply to build better CAR-NK therapies. In particular, we explore the importance of optimizing the immunochemical properties of the CAR construct, understanding factors leading to cell product persistence, enhancing trafficking of transferred cells to the tumor, ensuring the metabolic fitness of the transferred product, and strategies to avoid tumor escape through antigen loss. We also review trogocytosis, an important emerging challenge that likely equally applies to CAR-T and CAR-NK cells. Finally, we discuss how these limitations are already being addressed in CAR-NK therapies, and what future directions may be possible.

摘要

嵌合抗原受体工程化 T 细胞(CAR-T)疗法在过去十年中为多种癌症类型的治疗带来了革命性的变化。尽管取得了这一成功,但包括高昂的价格标签、制造复杂性和治疗相关毒性在内的障碍限制了这种疗法的广泛应用。嵌合抗原受体工程化自然杀伤细胞(CAR-NK)疗法为更简单、更经济实惠的“现成”治疗提供了一个潜在的机会,可能毒性更小。与 CAR-T 不同,CAR-NK 疗法仍处于早期开发阶段,目前报道的临床试验很少。鉴于 CAR-T 疗法开发过程中遇到的挑战,本综述探讨了我们可以应用哪些经验教训来构建更好的 CAR-NK 疗法。特别是,我们探讨了优化 CAR 构建体免疫化学特性、了解导致细胞产品持久性的因素、增强转导细胞向肿瘤的迁移、确保转导产物的代谢适应性以及避免通过抗原丢失发生肿瘤逃逸的策略的重要性。我们还回顾了 trogocytosis,这是一个重要的新兴挑战,可能同样适用于 CAR-T 和 CAR-NK 细胞。最后,我们讨论了这些限制因素在 CAR-NK 疗法中是如何被解决的,以及未来可能的发展方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d56/10187144/87bdfc9a3ef2/fimmu-14-1166038-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d56/10187144/6c83f2053b3c/fimmu-14-1166038-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d56/10187144/87bdfc9a3ef2/fimmu-14-1166038-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d56/10187144/6c83f2053b3c/fimmu-14-1166038-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d56/10187144/87bdfc9a3ef2/fimmu-14-1166038-g002.jpg

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Simultaneous engineering of natural killer cells for CAR transgenesis and CRISPR-Cas9 knockout using retroviral particles.使用逆转录病毒颗粒对自然杀伤细胞进行同时工程改造以实现嵌合抗原受体(CAR)转基因和CRISPR-Cas9基因敲除。
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