CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Chimeric Antigen Receptor T Cell Manufacturing on an Automated Cell Processor.
Chimeric Antigen Receptor T Cell Manufacturing on an Automated Cell Processor.
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嵌合抗原受体(CAR)T 细胞是治疗多种恶性和非恶性疾病的一种有前景的免疫疗法。CAR-T 细胞是经基因修饰的 T 细胞,可表达能够识别并结合细胞表面靶点的嵌合蛋白,进而杀伤靶细胞。传统 CAR-T 细胞生产方法劳动强度大、成本高,并可能存在污染风险。CliniMACS Prodigy 是一种自动化细胞处理器,可在封闭系统中以临床规模生产细胞治疗产品,从而最大程度降低污染风险。该处理过程在计算机控制下半自动运行,可减少人工参与,节省时间并降低变异和错误。本文及配套视频介绍如何使用该处理器进行 T 细胞转导(TCT)流程以生产 CAR-T 细胞。TCT 流程包括 CD4⁺/CD8⁺ T 细胞富集、活化、病毒载体转导、扩增和收获。借助 Activity Matrix 功能,可对这些步骤进行排序和计时,从而大幅定制 TCT 流程。
我们逐步介绍符合现行药品生产质量管理规范(cGMP)的 CAR-T 细胞生产,并讨论支持新药临床试验申请(IND)所需的放行检测和临床前实验。
我们展示了使用半自动流程进行临床 CAR-T 细胞生产的可行性,并讨论其优势与不足。最后,我们以一项正在开展的研究者发起临床试验为例,说明该生产流程如何应用于临床;该试验靶向儿童 B 细胞恶性肿瘤(NCT05480449)。
Chimeric antigen receptor (CAR)-T cells represent a promising immunotherapeutic approach for the treatment of various malignant and non-malignant diseases. CAR-T cells are genetically modified T cells that express a chimeric protein that recognizes and binds to a cell surface target, resulting in the killing of the target cell. Traditional CAR-T cell manufacturing methods are labor-intensive, expensive, and may carry the risk of contamination. The CliniMACS Prodigy, an automated cell processor, allows for manufacturing cell therapy products at a clinical scale in a closed system, minimizing the risk of contamination.
Processing occurs semi-automatically under the control of a computer and thus minimizes human involvement in the process, which saves time and reduces variability and errors. This manuscript and video describes the T cell transduction (TCT) process for manufacturing CAR-T cells using this processor.
The TCT process involves CD4+/CD8+ T cell enrichment, activation, transduction with a viral vector, expansion, and harvest. Using the Activity Matrix, a functionality that allows ordering and timing of these steps, the TCT process can be customized extensively.
We provide a walk-through of CAR-T cell manufacturing in compliance with current Good Manufacturing Practice (cGMP) and discuss required release testing and preclinical experiments that will support an Investigational New Drug (IND) application.
We demonstrate the feasibility and discuss the advantages and disadvantages of using a semi-automatic process for clinical CAR-T cell manufacturing.
Finally, we describe an ongoing investigator-initiated clinical trial that targets pediatric B-cell malignancies [NCT05480449] as an example of how this manufacturing process can be applied in a clinical setting.
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