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整合生物材料与 CAR-T 细胞以增强实体瘤治疗的研究进展

英文原题:Advances in integrating biomaterials with CAR-T cells for enhancing solid tumor therapy.

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Advances in integrating biomaterials with CAR-T cells for enhancing solid tumor therapy.

PubMed 2025/10/30(内容时间) Chin J Cancer Res Q1 · IF 6.7(JCR 2025)

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中文摘要

CAR-T(CAR-T)细胞免疫疗法已成为免疫肿瘤学中一种变革性的治疗模式。然而,CAR-T 疗法在实体瘤中的临床转化仍受到物理屏障、免疫抑制性肿瘤微环境(TME)以及治疗相关毒性的显著限制。生物材料领域的进展已展现出巨大潜力,可通过与CAR-T 细胞的协同整合来应对这些制约因素。本综述系统考察了CAR-T 细胞与多种生物材料平台联合应用的治疗策略,包括纳米颗粒、抗体功能化系统以及水凝胶。文章对生物材料在增强CAR-T 疗效中的多方面作用进行了批判性分析,具体包括促进T细胞活化与增殖、改善肿瘤靶向性以及重编程免疫抑制性TME。总体而言,本综述对CAR-T 与生物材料整合策略进行了全面分析,为推进实体瘤治疗提供了机制性与转化性见解。

展开英文摘要原文

Chimeric antigen receptor T (CAR-T) cell immunotherapy has emerged as a transformative modality in immuno-oncology.

However, the clinical translation of CAR-T therapy for solid tumors remains significantly limited by physical barriers, an immunosuppressive tumor microenvironment (TME), and treatment-related toxicities. Advances in biomaterials have demonstrated substantial potential to address these constraints through synergistic integration with CAR-T cells. This review systematically examines therapeutic applications of CAR-T cells combined with diverse biomaterial platforms, including nanoparticles, antibody-functionalized systems, and hydrogels.

Critical analysis is provided on the multifaceted roles of biomaterials in enhancing CAR-T efficacy, specifically by promoting T cell activation and proliferation, improving tumor targeting, and reprogramming the immunosuppressive TME. Collectively, this review delivers a comprehensive analysis of CAR-T-biomaterial integration strategies, offering mechanistic and translational insights to advance solid tumor therapies.

论文信息

作者
Huang S、Zhao Y、Shen J
单位
Comprehensive Cancer Center, Department of Oncology, Nanjing Drum Tower Hospital & Group's Suqian Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing 210008, China.China
期刊
Chinese journal of cancer research = Chung-kuo yen cheng yen chiu2025 Oct 30
原文标识
PubMed 41229983 · DOI 10.21147/j.issn.1000-9604.2025.05.07