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用于实体瘤增强型过继性细胞转移治疗的不同尺寸生物材料

[Biomaterials of different sizes for enhanced adoptive cell transfer therapy in solid tumors].

作者信息

Chen Jiaxin, Liu Rui, Tang Yingqi, Qian Chenggen

机构信息

Department of Pharmaceutics, School of Pharmacy, China Pharmaceutical University, State Key Laboratory of Natural Medicines, Nanjing 210009, China.

出版信息

Zhejiang Da Xue Xue Bao Yi Xue Ban. 2025 Jul 15;54(4):469-478. doi: 10.3724/zdxbyxb-2024-0651.


DOI:10.3724/zdxbyxb-2024-0651
PMID:40660877
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12382318/
Abstract

Adoptive cell transfer (ACT) shows significant efficacy against hema-tological malignancies but is limited in solid tumors due to poor homing, immunosuppre-ssion, and potential toxicity. Biomaterials spanning from nano- to macroscales-including nanoparticles, microspheres/micropatches, and hydrogels-offer unique advantages for cell engineering, delivery, and modulation of the tumor microenvironment. Specifically, nanoparticles enable gene delivery, artificial antigen-presenting cell engi-neering, and immune microenvironment remodeling. Microspheres/micropatches improve immune cell expansion, targeted activation, and localized retention. Hydrogels enhance ACT via genetic engineering, 3D culture support, and cytokine co-delivery. This review summarizes advances in biomaterial-enhanced ACT, highlighting their potential to improve delivery efficiency, amplify antitumor responses, and reduce toxicity. These insights may accelerate the clinical translation of ACT for solid tumors.

摘要

过继性细胞转移(ACT)对血液系统恶性肿瘤显示出显著疗效,但由于归巢能力差、免疫抑制和潜在毒性,在实体瘤治疗中受到限制。从纳米到宏观尺度的生物材料——包括纳米颗粒、微球/微贴片和水凝胶——在细胞工程、递送以及肿瘤微环境调控方面具有独特优势。具体而言,纳米颗粒可实现基因递送、人工抗原呈递细胞工程以及免疫微环境重塑。微球/微贴片可改善免疫细胞扩增、靶向激活和局部滞留。水凝胶通过基因工程、三维培养支持和细胞因子共递送增强ACT。本综述总结了生物材料增强ACT的进展,强调了它们在提高递送效率、增强抗肿瘤反应和降低毒性方面的潜力。这些见解可能会加速ACT在实体瘤治疗中的临床转化。

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[Biomaterials of different sizes for enhanced adoptive cell transfer therapy in solid tumors].

Zhejiang Da Xue Xue Bao Yi Xue Ban. 2025-7-15

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本文引用的文献

[1]
Emerging frontiers in adoptive cell therapies: innovations, challenges, and future perspectives.

Med Oncol. 2025-6-15

[2]
Smart Polymer Microspheres: Preparation, Microstructures, Stimuli-Responsive Properties, and Applications.

ACS Nano. 2025-5-20

[3]
Targeted LNPs deliver IL-15 superagonists mRNA for precision cancer therapy.

Biomaterials. 2025-6

[4]
Augmentation of Solid Tumor Immunotherapy With IL-12.

J Gene Med. 2024-12

[5]
Spiky Gold Nanoparticles, a Nanoscale Approach to Enhanced Ex Vivo T-Cell Activation.

ACS Nano. 2024-8-13

[6]
Subcutaneous biodegradable scaffolds for restimulating the antitumour activity of pre-administered CAR-T cells.

Nat Biomed Eng. 2025-2

[7]
CAR-T cell therapy: Efficacy in management of cancers, adverse effects, dose-limiting toxicities and long-term follow up.

Int Immunopharmacol. 2024-6-30

[8]
Optimizing Transfection Efficiency in CAR-T Cell Manufacturing through Multiple Administrations of Lipid-Based Nanoparticles.

ACS Appl Bio Mater. 2024-6-17

[9]
T Cell and Natural Killer Cell Membrane-Camouflaged Nanoparticles for Cancer and Viral Therapies.

ACS Appl Bio Mater. 2024-5-20

[10]
encapsulation and expansion of T and CAR-T cells using 3D synthetic thermo-responsive matrices.

RSC Adv. 2024-4-26

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