← 返回

用于快速体内制备与释放 CAR-T 细胞的生物指令性可植入支架

英文原题:Bioinstructive implantable scaffolds for rapid in vivo manufacture and release of CAR-T cells.

查看英文原题

Bioinstructive implantable scaffolds for rapid in vivo manufacture and release of CAR-T cells.

PubMed 2022/03/24(内容时间) Nat Biotechnol Q1 · IF 44.5(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

尽管其在临床上取得了成功,针对B细胞恶性肿瘤的嵌合抗原受体(CAR)-T细胞疗法仍受限于冗长、昂贵且劳动密集的体外制造流程,这可能导致细胞产品组成异质性。在此,我们描述了一种用于T细胞工程与释放的可植入多功能藻酸盐支架(MASTER),它简化了体内CAR-T 细胞制造,并将处理时间缩短至一天。当接种人类外周血单核细胞和编码CD19的逆转录病毒颗粒时,MASTER为病毒载体介导的基因转移提供了适当的界面,并且皮下植入后,在小鼠中介导功能性CAR-T 细胞的释放。我们进一步证明,在淋巴瘤小鼠异种移植模型中,体内生成的CAR-T 细胞进入血流并控制远端肿瘤生长,显示出比传统CAR-T 细胞更强的持久性。MASTER有望通过快速制造并可能减少提供此类疗法所需的复杂性和资源,来转变CAR-T 细胞疗法。

展开英文摘要原文

Despite their clinical success, chimeric antigen receptor (CAR)-T cell therapies for B cell malignancies are limited by lengthy, costly and labor-intensive ex vivo manufacturing procedures that might lead to cell products with heterogeneous composition.

Here we describe an implantable Multifunctional Alginate Scaffold for T Cell Engineering and Release (MASTER) that streamlines in vivo CAR-T cell manufacturing and reduces processing time to a single day. When seeded with human peripheral blood mononuclear cells and CD19-encoding retroviral particles, MASTER provides the appropriate interface for viral vector-mediated gene transfer and, after subcutaneous implantation, mediates the release of functional CAR-T cells in mice.

We further demonstrate that in vivo-generated CAR-T cells enter the bloodstream and control distal tumor growth in a mouse xenograft model of lymphoma, showing greater persistence than conventional CAR-T cells. MASTER promises to transform CAR-T cell therapy by fast-tracking manufacture and potentially reducing the complexity and resources needed for provision of this type of therapy.

论文信息

作者
Agarwalla P、Ogunnaike EA、Ahn S、Froehlich KA、Jansson A、Ligler FS、Dotti G、Brudno Y
第一作者单位
Joint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University, Raleigh, NC, USA.United States
通讯作者单位
Joint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University, Raleigh, NC, USA. ybrudno@ncsu.edu.United States
文献类型
非美国政府资助研究 · 美国 NIH 资助研究 · 美国政府(非公共卫生署)资助研究
期刊
Nature biotechnology2022 Aug
原文标识
PubMed 35332339 · DOI 10.1038/s41587-022-01245-x