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通过合成生物学增强嵌合抗原受体自然杀伤细胞的生理特性。

Enhancing the physiological characteristics of chimeric antigen receptor natural killer cells by synthetic biology.

作者信息

Ji Shuochao, Jin Cheng, Cui Xinjiang

机构信息

Affiliated Hospital of Shandong Second Medical University, Weifang, China.

Department of Hematology and Oncology, Shenzhen Children's Hospital, Shenzhen, China.

出版信息

Front Immunol. 2025 Apr 17;16:1592121. doi: 10.3389/fimmu.2025.1592121. eCollection 2025.


DOI:10.3389/fimmu.2025.1592121
PMID:40313937
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12043574/
Abstract

Chimeric antigen receptor natural Killer (CAR-NK) cells therapy represents a next-generation immunotherapeutic approach following CAR-T cells therapy, offering inherent "off-the-shelf" compatibility and mitigated off-tumor toxicity. Despite these advantages, clinical translation remains constrained by poor persistence and functional exhaustion in immunosuppressive tumor microenvironments (TME). This review examines recent advancements in synthetic biology aimed at enhancing the physiological characteristics of CAR-NK cells. By delineating the synergy between NK cells and synthetic biology toolkits, this work provides a roadmap for developing next-generation CAR-NK therapies capable of addressing solid tumor challenges while maintaining favorable safety profiles.

摘要

嵌合抗原受体自然杀伤(CAR-NK)细胞疗法是继CAR-T细胞疗法之后的新一代免疫治疗方法,具有固有的“现成可用”兼容性且能减轻肿瘤外毒性。尽管有这些优势,但临床转化仍受到免疫抑制性肿瘤微环境(TME)中CAR-NK细胞持久性差和功能耗竭的限制。本综述探讨了旨在增强CAR-NK细胞生理特性的合成生物学的最新进展。通过阐述自然杀伤细胞与合成生物学工具包之间的协同作用,这项工作为开发能够应对实体瘤挑战同时保持良好安全性的下一代CAR-NK疗法提供了路线图。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd5f/12043574/8021f8fb06fe/fimmu-16-1592121-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd5f/12043574/c465b11f6db8/fimmu-16-1592121-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd5f/12043574/8021f8fb06fe/fimmu-16-1592121-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd5f/12043574/c465b11f6db8/fimmu-16-1592121-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd5f/12043574/8021f8fb06fe/fimmu-16-1592121-g002.jpg

相似文献

[1]
Enhancing the physiological characteristics of chimeric antigen receptor natural killer cells by synthetic biology.

Front Immunol. 2025-4-17

[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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引用本文的文献

[1]
Overcoming Immune Barriers in Allogeneic CAR-NK Therapy: From Multiplex Gene Editing to AI-Driven Precision Design.

Biomolecules. 2025-6-26

本文引用的文献

[1]
Bacterial immunotherapy leveraging IL-10R hysteresis for both phagocytosis evasion and tumor immunity revitalization.

Cell. 2025-4-3

[2]
Chimeric cytokine receptor TGF-β RⅡ/IL-21R improves CAR-NK cell function by reversing the immunosuppressive tumor microenvironment of gastric cancer.

Pharmacol Res. 2025-2

[3]
Hyperacute rejection-engineered oncolytic virus for interventional clinical trial in refractory cancer patients.

Cell. 2025-2-20

[4]
Emerging combined CAR-NK cell therapies in cancer treatment: Finding a dancing partner.

Mol Ther. 2025-1-3

[5]
GLUT1 overexpression in CAR-T cells induces metabolic reprogramming and enhances potency.

Nat Commun. 2024-10-6

[6]
CRISPR/Cas9 editing of NKG2A improves the efficacy of primary CD33-directed chimeric antigen receptor natural killer cells.

Nat Commun. 2024-9-30

[7]
Engineered CAR-NK Cells with Tolerance to H2O2 and Hypoxia Can Suppress Postoperative Relapse of Triple-Negative Breast Cancers.

Cancer Immunol Res. 2024-11-4

[8]
CD19/CD20 dual-targeted chimeric antigen receptor-engineered natural killer cells exhibit improved cytotoxicity against acute lymphoblastic leukemia.

J Transl Med. 2024-3-13

[9]
CAR-Toner: an AI-driven approach for CAR tonic signaling prediction and optimization.

Cell Res. 2024-5

[10]
Co-expression of IL-21-Enhanced NKG2D CAR-NK cell therapy for lung cancer.

BMC Cancer. 2024-1-23

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