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嵌合抗原受体疗法与信使核糖核酸技术相遇。

Chimeric antigen receptor therapy meets mRNA technology.

作者信息

Wu Jiacai, Wu Weigang, Zhou Boping, Li Bin

机构信息

Department of Infectious Disease, Shenzhen People's Hospital, The First Affiliated Hospital of Southern University of Science and Technology and The Second Clinical Medical College of Jinan University, Shenzhen 518020, China; School of Medicine, Southern University of Science and Technology, Shenzhen, 518055, China.

Department of Infectious Disease, Shenzhen People's Hospital, The First Affiliated Hospital of Southern University of Science and Technology and The Second Clinical Medical College of Jinan University, Shenzhen 518020, China.

出版信息

Trends Biotechnol. 2024 Feb;42(2):228-240. doi: 10.1016/j.tibtech.2023.08.005. Epub 2023 Sep 21.

DOI:10.1016/j.tibtech.2023.08.005
PMID:37741706
Abstract

Genetically engineered immune cells expressing chimeric antigen receptors (CARs) have emerged as a new game changer in cancer immunotherapy. The utility of CAR T cell therapy against hematological malignancies has been validated in clinical practice. Other CAR immune cells are currently under investigation to improve the potency of CAR therapy in solid tumors. As a new class of therapeutic modalities, mRNA-based therapeutics hold enormous potential beyond COVID-19 mRNA vaccines. Arming immune cells with mRNA-encoded CARs represents a new frontier in cancer and beyond, enabling in vivo generation of CAR cells without causing transgene integration. In this review, we summarize recent advances in mRNA-based CAR immunotherapies and highlight their opportunities and challenges for the development of a new generation of living drugs.

摘要

表达嵌合抗原受体(CAR)的基因工程免疫细胞已成为癌症免疫治疗中的一种新的变革力量。CAR-T细胞疗法针对血液系统恶性肿瘤的效用已在临床实践中得到验证。目前正在研究其他CAR免疫细胞,以提高CAR疗法在实体瘤中的效力。作为一类新的治疗方式,基于mRNA的疗法在COVID-19 mRNA疫苗之外具有巨大潜力。用mRNA编码的CAR武装免疫细胞代表了癌症及其他领域的一个新前沿,能够在体内生成CAR细胞而不导致转基因整合。在本综述中,我们总结了基于mRNA的CAR免疫疗法的最新进展,并强调了其在新一代活体药物开发中的机遇和挑战。

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Chimeric antigen receptor therapy meets mRNA technology.嵌合抗原受体疗法与信使核糖核酸技术相遇。
Trends Biotechnol. 2024 Feb;42(2):228-240. doi: 10.1016/j.tibtech.2023.08.005. Epub 2023 Sep 21.
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In Vitro-Transcribed mRNA Chimeric Antigen Receptor T Cell (IVT mRNA CAR T) Therapy in Hematologic and Solid Tumor Management: A Preclinical Update.体外转录信使 RNA 嵌合抗原受体 T 细胞(IVT mRNA CAR T)疗法在血液系统恶性肿瘤和实体瘤治疗中的临床前进展。
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Recent findings on chimeric antigen receptor (CAR)-engineered immune cell therapy in solid tumors and hematological malignancies.近期关于嵌合抗原受体(CAR)修饰免疫细胞治疗实体瘤和血液恶性肿瘤的研究进展。
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Nanotechnology-based chimeric antigen receptor T-cell therapy in treating solid tumor.基于纳米技术的嵌合抗原受体 T 细胞疗法治疗实体瘤。
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Tuning CARs: recent advances in modulating chimeric antigen receptor (CAR) T cell activity for improved safety, efficacy, and flexibility.调整 CAR:修饰嵌合抗原受体 (CAR) T 细胞活性以提高安全性、疗效和灵活性的最新进展。
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Chimeric antigen-receptor T-cell therapy for hematological malignancies and solid tumors: Clinical data to date, current limitations and perspectives.嵌合抗原受体 T 细胞疗法治疗血液系统恶性肿瘤和实体瘤:临床数据现状、当前局限性和展望。
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CAR-engineered NK cells; a promising therapeutic option for treatment of hematological malignancies.嵌合抗原受体修饰的自然杀伤细胞;治疗血液系统恶性肿瘤的一种很有前途的治疗选择。
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引用本文的文献

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CAR T-cell therapy in autoimmune diseases: a promising frontier on the horizon.自身免疫性疾病中的嵌合抗原受体T细胞疗法:一个充满前景的前沿领域。
Front Immunol. 2025 Aug 12;16:1613878. doi: 10.3389/fimmu.2025.1613878. eCollection 2025.
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Lung metastasis and recurrence is mitigated by CAR macrophages, in-situ-generated from mRNA delivered by small extracellular vesicles.由小细胞外囊泡递送的mRNA原位生成的CAR巨噬细胞可减轻肺转移和复发。
Nat Commun. 2025 Aug 4;16(1):7166. doi: 10.1038/s41467-025-62506-2.
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Research progress on chimeric antigen receptor-based immunotherapy against autoimmune diseases.
基于嵌合抗原受体的自身免疫性疾病免疫治疗研究进展
Hum Vaccin Immunother. 2025 Dec;21(1):2538350. doi: 10.1080/21645515.2025.2538350. Epub 2025 Aug 1.
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RNA Therapeutics: Focus on Antisense Oligonucleotides in the Nervous System.RNA疗法:聚焦于神经系统中的反义寡核苷酸
Biomol Ther (Seoul). 2025 Jun 19. doi: 10.4062/biomolther.2025.022.
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Revolutionizing Autoimmune Kidney Disease Treatment with Chimeric Antigen Receptor-T Cell Therapy.嵌合抗原受体 T 细胞疗法革新自身免疫性肾病治疗
Research (Wash D C). 2025 May 22;8:0712. doi: 10.34133/research.0712. eCollection 2025.
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Structure-guided design of endosomolytic chloroquine-like lipid nanoparticles for mRNA delivery and genome editing.用于mRNA递送和基因组编辑的溶酶体裂解型氯喹样脂质纳米颗粒的结构导向设计
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