嵌合抗原受体
细胞毒性T细胞
化学
T细胞
人类免疫缺陷病毒(HIV)
抗体
细胞
细胞毒性
CD3型
病毒学
细胞培养
抗原
癌症治疗
免疫疗法
慢病毒
遗传增强
Jurkat细胞
癌细胞
癌症
病毒
病毒载体
固体脂质纳米粒
CD8型
免疫系统
癌症免疫疗法
纳米颗粒
癌症研究
生物
纳米技术
药物输送
基因传递
载体(分子生物学)
细胞生物学
作者
D K Kim,So-Jeong Moon,Emily L. Han,Ellie Feng,Amanda M. Murray,Jinjin Wang,Wei Liu,Gu Kong,Carl H. June,Michael J. Mitchell
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-04-21
标识
DOI:10.1021/acs.nanolett.5c06317
摘要
Chimeric antigen receptor (CAR)-T therapy has led to remarkable advancements in the treatment of hematologic malignancies, encouraging extensive studies on its application to solid tumors and other diseases. However, the production of CAR-T cells is mostly achieved through viral transduction, which results in permanent CAR expression in T cells, potentially leading to unintended adverse effects. Here, we present a lipid nanoparticle (LNP) platform for mRNA delivery to human primary T cells, inspired by the human immunodeficiency virus (HIV) which naturally infects T cells. We perform multiple rounds of screening to sequentially optimize the structure and ratio of ionizable lipid in the base formulation, the ratios of HIV lipid components, and the type and ratio of PEG-lipid for CD3 antibody conjugation. Our HIV envelope-Inspired T cell transfection-Enhancing (HITE) LNP enables efficient generation of CAR-T cells with potent cytotoxic activity against cancer cells in vitro, demonstrating its potential for efficient CAR-T cell production.
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