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嵌合抗原受体 T 细胞(CAR-T)和嵌合抗原受体自然杀伤细胞(CAR-NK)作为实体瘤的细胞癌症免疫疗法。

CAR-T and CAR-NK as cellular cancer immunotherapy for solid tumors.

机构信息

Department of Genetics, Yale University School of Medicine, New Haven, CT, USA.

System Biology Institute, Yale University, West Haven, CT, USA.

出版信息

Cell Mol Immunol. 2024 Oct;21(10):1089-1108. doi: 10.1038/s41423-024-01207-0. Epub 2024 Aug 12.

DOI:10.1038/s41423-024-01207-0
PMID:39134804
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11442786/
Abstract

In the past decade, chimeric antigen receptor (CAR)-T cell therapy has emerged as a promising immunotherapeutic approach for combating cancers, demonstrating remarkable efficacy in relapsed/refractory hematological malignancies in both pediatric and adult patients. CAR-natural killer (CAR-NK) cell complements CAR-T cell therapy by offering several distinct advantages. CAR-NK cells do not require HLA compatibility and exhibit low safety concerns. Moreover, CAR-NK cells are conducive to "off-the-shelf" therapeutics, providing significant logistic advantages over CAR-T cells. Both CAR-T and CAR-NK cells have shown consistent and promising results in hematological malignancies. However, their efficacy against solid tumors remains limited due to various obstacles including limited tumor trafficking and infiltration, as well as an immuno-suppressive tumor microenvironment. In this review, we discuss the recent advances and current challenges of CAR-T and CAR-NK cell immunotherapies, with a specific focus on the obstacles to their application in solid tumors. We also analyze in depth the advantages and drawbacks of CAR-NK cells compared to CAR-T cells and highlight CAR-NK CAR optimization. Finally, we explore future perspectives of these adoptive immunotherapies, highlighting the increasing contribution of cutting-edge biotechnological tools in shaping the next generation of cellular immunotherapy.

摘要

在过去的十年中,嵌合抗原受体 (CAR)-T 细胞疗法已成为一种有前途的免疫治疗方法,用于治疗癌症,在儿科和成年患者的复发/难治性血液恶性肿瘤中显示出显著的疗效。CAR-自然杀伤 (CAR-NK) 细胞通过提供几个明显的优势来补充 CAR-T 细胞疗法。CAR-NK 细胞不需要 HLA 相容性,并且安全性问题较低。此外,CAR-NK 细胞有利于“现货”治疗,与 CAR-T 细胞相比具有显著的物流优势。CAR-T 和 CAR-NK 细胞在血液恶性肿瘤中均显示出一致且有前途的结果。然而,由于包括有限的肿瘤运输和浸润以及免疫抑制性肿瘤微环境在内的各种障碍,它们对实体瘤的疗效仍然有限。在这篇综述中,我们讨论了 CAR-T 和 CAR-NK 细胞免疫疗法的最新进展和当前挑战,特别关注它们在实体瘤中应用的障碍。我们还深入分析了 CAR-NK 细胞与 CAR-T 细胞相比的优缺点,并强调了 CAR-NK CAR 的优化。最后,我们探讨了这些过继免疫疗法的未来前景,强调了尖端生物技术工具的日益贡献,塑造了下一代细胞免疫疗法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb8a/11442786/e5ddb0ab9dc5/41423_2024_1207_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb8a/11442786/68146f53e93d/41423_2024_1207_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb8a/11442786/cac6f97d8f21/41423_2024_1207_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb8a/11442786/ad8683dd5f88/41423_2024_1207_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb8a/11442786/a44959bda417/41423_2024_1207_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb8a/11442786/e5ddb0ab9dc5/41423_2024_1207_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb8a/11442786/68146f53e93d/41423_2024_1207_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb8a/11442786/cac6f97d8f21/41423_2024_1207_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb8a/11442786/ad8683dd5f88/41423_2024_1207_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb8a/11442786/a44959bda417/41423_2024_1207_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb8a/11442786/e5ddb0ab9dc5/41423_2024_1207_Fig5_HTML.jpg

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3
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