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用于制备疗效增强的 CAR-T 细胞的葡聚糖基 T 细胞扩增纳米颗粒

英文原题:Dextran-based T-cell expansion nanoparticles for manufacturing CAR T cells with augmented efficacy.

查看英文原题

Dextran-based T-cell expansion nanoparticles for manufacturing CAR T cells with augmented efficacy.

PubMed 2026/01/20(内容时间) Nat Commun Q1 · IF 18.1(JCR 2025)

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中文摘要

目前正在多个白血病/淋巴瘤以外的癌种中探索采用嵌合抗原受体(CAR)工程化T细胞的过继T细胞疗法。CAR-T 细胞制备的关键步骤是T细胞活化与扩增,这有助于病毒转导,但也可能损害T细胞适能并降低其体内持久性。研究者开发了用于T细胞活化和扩增的“T-Expand”,由偶联抗CD3和抗CD28抗体的葡聚糖纳米颗粒构成。该纳米颗粒可强效多克隆扩增人T细胞,效率与商业化微珠(Dynabeads)相当。在T-Expand存在时制备的CD19 CAR-T 细胞,在体外增殖能力、细胞毒性和持久性均增强;在小鼠模型中也表现出强效抗淋巴瘤活性,仅需四分之一CAR-T 细胞剂量即可完全清除肿瘤。

重要的是,T-Expand具有生物相容性,未观察到毒性;与Dynabeads相比,T细胞扩增后无需去除颗粒。作为一种生物相容性T细胞扩增平台,T-Expand简化了制备流程,同时增强T细胞持久性和功能,因此有望提高CAR-T 细胞疗法的临床疗效。

展开英文摘要原文

Adoptive T cell therapy using chimeric antigen receptor (CAR) engineered T cells is currently being explored in multiple cancer types beyond leukemia/lymphoma. A key step in CAR-T cell manufacturing is the activation and expansion of T cells, which facilitates viral transduction, however, may hamper T cell fitness and reduce in vivo persistence. "T-Expand" is developed for T cell activation and expansion, comprising dextran-based nanoparticles conjugated with anti-CD3 and anti-CD28 antibodies.

The nanoparticles trigger robust polyclonal expansion of human T cells with efficiency in the range of commercial microbeads (Dynabeads ). Engineered in the presence of T-Expand, CD19 CAR T cells display enhanced proliferative capacity, cytotoxicity and persistence in vitro, and furthermore, exhibit potent anti-lymphoma activity in mouse models, resulting in complete tumor clearance at one fourth of the CAR T cell dose.

Importantly, T-Expand is biocompatible with no observed toxicity, circumventing removal steps after T cell expansion compared to Dynabeads TM . As a biocompatible T cell expansion platform, T-Expand simplifies the manufacturing process while enhancing T cell persistence and functionality, and thereby holds promise for increasing clinical efficacy of CAR T cell therapy.

论文信息

作者
Zheng T、Ramanathan K、Ormhøj M、Hansen MR、Halldórsdóttir HR、Li H、Munk KK、Rodriguez-Pardo C
第一作者单位
Experimental and Translational Immunology Section, Department for Health Technology, Technical University of Denmark, Lyngby, Denmark.Denmark
通讯作者单位
Experimental and Translational Immunology Section, Department for Health Technology, Technical University of Denmark, Lyngby, Denmark. sirha@dtu.dk.Denmark
期刊
Nature communications2026 Jan 20
原文标识
PubMed 41559042 · DOI 10.1038/s41467-025-67868-1