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迈向体内 CAR-T 细胞治疗:完善 CAR 与脂质纳米颗粒设计

英文原题:Toward In Vivo CAR T Cell Therapy: Perfecting CAR and Lipid Nanoparticle Design.

查看英文原题

Toward In Vivo CAR T Cell Therapy: Perfecting CAR and Lipid Nanoparticle Design.

PubMed 2026/02/11(内容时间) Nano Lett Q1 · IF 9.1(JCR 2025)

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中文摘要

CAR-T 细胞疗法是治疗血液系统癌症的主要疗法之一,但传统体外制备过程极其复杂、昂贵且耗时。因此,体内CAR-T 疗法成为有前景的替代方案,可直接在患者体内对T细胞进行基因改造。这一新方法需要谨慎设计三个模块化且相互依赖的纳米尺度参数:CAR结构、靶向脂质纳米颗粒递送系统及核酸载荷形式。各组成部分具有高度模块化特征,因此系统优化可提高体内生成CAR-T 细胞的安全性和疗效。本文回顾这一治疗策略的分子和机制原理,重点阐述这些纳米尺度设计特征如何影响体内CAR-T 细胞生成及功能表现。深入理解这些参数对于开发高效、安全且具临床转化潜力的体内CAR-T 癌症疗法至关重要。

展开英文摘要原文

CAR T cell therapy represents a leading therapeutic modality in the treatment of hematological cancers.

However, conventional ex vivo manufacturing processes are extremely complex, costly, and time-consuming. Hence, in vivo CAR-T cell therapy represents a promising alternative, where T cells are genetically modified directly within the patient.

This novel approach requires the careful design of three modular and interdependent nanoscale parameters: CAR architecture, targeted lipid nanoparticle delivery systems, and nucleic acid cargo format. Each component is highly modular, therefore systematic optimization can enhance the safety and efficacy of in vivo CAR T cell generation.

Here, we review the molecular and mechanistic principles underlying this therapeutic strategy, emphasizing how these nanoscale design features govern CAR T cell production and functional performance in vivo. Advancing our understanding of these parameters is critical to developing efficient, safe, and clinically translatable in vivo CAR T cell cancer therapies.

论文信息

作者
Sciuto L、Kooijmans SAA、Schiffelers RM
单位
CDL Research, Division LAB, University Medical Center Utrecht, Heidelberglaan 100, 3584 CX Utrecht, The Netherlands.Netherlands
文献类型
综述 · 非美国政府资助研究
期刊
Nano letters2026 Feb 25
原文标识
PubMed 41672452 · DOI 10.1021/acs.nanolett.5c05535