离体
纳米技术
T细胞
汽车T细胞治疗
纳米医学
细胞
体内
癌症治疗
模块化设计
细胞疗法
癌症
材料科学
嵌合抗原受体
计算生物学
化学
纳米颗粒
免疫疗法
核酸
计算机科学
作者
Ludovica Sciuto,Sander A. A. Kooijmans,Schiffelers Rm
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-02-11
卷期号:26 (7): 2337-2347
被引量:3
标识
DOI:10.1021/acs.nanolett.5c05535
摘要
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.
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