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CAR-T 与 CAR-NK 作为实体瘤细胞免疫治疗

英文原题:CAR-T and CAR-NK as cellular cancer immunotherapy for solid tumors.

PubMed 2024/08/12(内容时间) Cell Mol Immunol Q1 · IF 23.9(JCR 2025)

研究概要

在过去十年中,嵌合抗原受体(CAR)-T细胞疗法已成为一种有前景的抗击癌症的免疫治疗方法,在儿童和成人复发/难治性血液系统恶性肿瘤中均显示出显著疗效。

中文摘要

在过去十年中,嵌合抗原受体(CAR)-T细胞疗法已成为一种有前景的抗癌免疫治疗方法,在儿童和成人复发/难治性血液系统恶性肿瘤中均显示出显著疗效。CAR-自然杀伤(CAR-NK)细胞通过提供若干独特优势,对CAR-T细胞疗法形成补充。CAR-NK细胞不需要HLA相容性,且安全性顾虑较低。此外,CAR-NK细胞有利于现货型治疗,与CAR-T细胞相比具有显著的物流优势。CAR-T和CAR-NK细胞在血液系统恶性肿瘤中均已显示出一致且有前景的结果。然而,由于多种障碍,包括向肿瘤的迁移和浸润受限,以及免疫抑制性肿瘤微环境,它们在实体瘤中的疗效仍然有限。在这篇综述中,我们讨论CAR-T和CAR-NK细胞免疫疗法的最新进展和当前挑战,特别关注其在实体瘤中应用的障碍。我们还深入分析CAR-NK细胞相较于CAR-T细胞的优势和缺点,并强调CAR-NK的CAR优化。最后,我们探讨这些过继性免疫疗法的未来前景,强调尖端生物技术工具在塑造下一代细胞免疫疗法中日益增加的贡献。

展开英文摘要原文

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.

论文信息

作者
Peng L、Sferruzza G、Yang L、Zhou L、Chen S
第一作者单位
Department of Genetics, Yale University School of Medicine, New Haven, CT, USA. l.peng@yale.edu.United States
通讯作者单位
Department of Genetics, Yale University School of Medicine, New Haven, CT, USA. sidi.chen@yale.edu.United States
文献类型
综述 · 非美国政府资助研究
期刊
Cellular & molecular immunology2024 Oct
原文标识
PubMed 39134804 · DOI 10.1038/s41423-024-01207-0