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下一代体内 CAR-T 扩增策略:解锁实体瘤中的持久抗肿瘤反应

英文原题:Next-generation in vivo CAR-T expansion strategies: Unlocking durable anti-tumor responses in solid tumors.

查看英文原题

Next-generation in vivo CAR-T expansion strategies: Unlocking durable anti-tumor responses in solid tumors.

PubMed 2026/04/19(内容时间) Crit Rev Oncol Hematol Q1 · IF 6.2(JCR 2025)

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中文摘要

CAR-T(CAR-T)细胞疗法的疗效与功能性活性抗肿瘤CAR-T 细胞的数量直接相关。然而,CAR-T 制备的复杂性限制了临床可及性,并增加了治疗准备期间疾病进展的风险。为了改进CAR-T 生产,已开发出多种策略以在体外或体内扩增CAR-T 细胞,包括基因工程、疫苗平台、细胞因子刺激,以及纳米颗粒、工程化细菌及其外膜囊泡(OMVs)的应用。随着体内CAR-T 方法的发展,开发能够实现安全有效体内扩增的生物相容性材料变得越来越重要。本综述系统性地探讨了实体瘤中体内CAR-T 细胞扩增所面临的挑战,全面总结了当前扩增平台的机制、优势与局限性,并讨论了其转化潜力,为指导体内CAR-T 疗法的开发提供了实用见解。

展开英文摘要原文

The efficacy of chimeric antigen receptor T (CAR-T) cell therapy is directly associated with the abundance of functionally active anti-tumor CAR-T cells.

However, the complexity of CAR-T manufacturing limits clinical accessibility and increases the risk of disease progression during treatment preparation. To improve CAR-T production, multiple strategies have been developed to expand CAR-T cells either in vitro or in vivo, including genetic engineering, vaccine platforms, cytokine stimulation, and the application of nanoparticles, engineered bacteria, and their outer membrane vesicles (OMVs).

With the advancement of in vivo CAR-T approaches, the development of biocompatible materials that enable safe and effective in vivo expansion has become increasingly important. This review systematically examines the challenges associated with in vivo CAR-T cell expansion in solid tumors, comprehensively summarizes the mechanisms, advantages, and limitations of current expansion platforms, and discusses their translational potential, providing practical insights to guide the development of in vivo CAR-T therapies.

论文信息

作者
Sun Z、Wei L、Pan X、Yan W、Wang T、Wang X
第一作者单位
The State Key Laboratory of Pharmaceutical Biotechnology, Division of Immunology, Medical School, Nanjing University, Nanjing 210093, China; Jiangsu Key Laboratory of Molecular Medicine, Division of Immunology, Medical School, Nanjing University, Nanjing 210093, China.China
通讯作者单位
The State Key Laboratory of Pharmaceutical Biotechnology, Division of Immunology, Medical School, Nanjing University, Nanjing 210093, China; Jiangsu Key Laboratory of Molecular Medicine, Division of Immunology, Medical School, Nanjing University, Nanjing 210093, China. Electronic address: wangxinyue@nju.edu.cn.China
文献类型
综述
期刊
Critical reviews in oncology/hematology2026 Jul
原文标识
PubMed 42013999 · DOI 10.1016/j.critrevonc.2026.105342