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嵌合抗原受体T细胞疗法的挑战与创新:全面分析

Challenges and innovations in CAR-T cell therapy: a comprehensive analysis.

作者信息

Luo Jingming, Zhang Xianwen

机构信息

College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha, China.

出版信息

Front Oncol. 2024 Jun 11;14:1399544. doi: 10.3389/fonc.2024.1399544. eCollection 2024.


DOI:10.3389/fonc.2024.1399544
PMID:38919533
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11196618/
Abstract

Recent years have seen a marked increase in research on chimeric antigen receptor T (CAR-T) cells, with specific relevance to the treatment of hematological malignancies. Here, the structural principles, iterative processes, and target selection of CAR-T cells for therapeutic applications are described in detail, as well as the challenges faced in the treatment of solid tumors and hematological malignancies. These challenges include insufficient infiltration of cells, off-target effects, cytokine release syndrome, and tumor lysis syndrome. In addition, directions in the iterative development of CAR-T cell therapy are discussed, including modifications of CAR-T cell structures, improvements in specificity using multi-targets and novel targets, the use of Boolean logic gates to minimize off-target effects and control toxicity, and the adoption of additional protection mechanisms to improve the durability of CAR-T cell treatment. This review provides ideas and strategies for the development of CAR-T cell therapy through an in-depth exploration of the underlying mechanisms of action of CAR-T cells and their potential for innovative modification.

摘要

近年来,嵌合抗原受体T(CAR-T)细胞的研究显著增加,尤其与血液系统恶性肿瘤的治疗相关。本文详细描述了用于治疗应用的CAR-T细胞的结构原理、迭代过程和靶点选择,以及在实体瘤和血液系统恶性肿瘤治疗中面临的挑战。这些挑战包括细胞浸润不足、脱靶效应、细胞因子释放综合征和肿瘤溶解综合征。此外,还讨论了CAR-T细胞疗法迭代发展的方向,包括CAR-T细胞结构的修饰、使用多靶点和新靶点提高特异性、使用布尔逻辑门最小化脱靶效应并控制毒性,以及采用额外的保护机制提高CAR-T细胞治疗的持久性。本综述通过深入探索CAR-T细胞的潜在作用机制及其创新修饰潜力,为CAR-T细胞疗法的发展提供思路和策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d491/11196618/07b5a8122953/fonc-14-1399544-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d491/11196618/1e67d3e38945/fonc-14-1399544-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d491/11196618/c5864adb2e37/fonc-14-1399544-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d491/11196618/07b5a8122953/fonc-14-1399544-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d491/11196618/1e67d3e38945/fonc-14-1399544-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d491/11196618/c5864adb2e37/fonc-14-1399544-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d491/11196618/07b5a8122953/fonc-14-1399544-g003.jpg

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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]
Comparative Analysis of Bispecific Antibodies and CAR T-Cell Therapy in Follicular Lymphoma.

Eur J Haematol. 2025-1

本文引用的文献

[1]
Low-dose targeted radionuclide therapy synergizes with CAR T cells and enhances tumor response.

Front Immunol. 2024

[2]
Novel CAR-T cells targeting TRKB for the treatment of solid cancer.

Apoptosis. 2024-12

[3]
Antigen Presenting Cell Mimetic Lipid Nanoparticles for Rapid mRNA CAR T Cell Cancer Immunotherapy.

Adv Mater. 2024-6

[4]
Mno Nanoenzyme Armed CAR-NK Cells Enhance Solid Tumor Immunotherapy by Alleviating the Immunosuppressive Microenvironment.

Adv Healthc Mater. 2024-4

[5]
SMAD7 expression in CAR-T cells improves persistence and safety for solid tumors.

Cell Mol Immunol. 2024-3

[6]
A dual-receptor T-cell platform with Ab-TCR and costimulatory receptor achieves specificity and potency against AML.

Blood. 2024-2-8

[7]
Construction of truncated PSMA as a PET reporter gene for CAR T cell trafficking.

J Leukoc Biol. 2024-2-23

[8]
CD19/CD22 targeting with cotransduced CAR T cells to prevent antigen-negative relapse after CAR T-cell therapy for B-cell ALL.

Blood. 2024-1-11

[9]
A distinct cytokine network distinguishes chimeric antigen receptor T cell (CAR-T)-associated hemophagocytic lymphohistiocytosis-like toxicity (carHLH) from severe cytokine release syndrome following CAR-T therapy.

Cytotherapy. 2023-11

[10]
LIGHT/TNFSF14 promotes CAR-T cell trafficking and cytotoxicity through reversing immunosuppressive tumor microenvironment.

Mol Ther. 2023-9-6

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