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可扩展的生物制造工作流程,用于生产和分离基于 NK 细胞来源的细胞外囊泡的癌症生物治疗药物

英文原题:Scalable Biomanufacturing Workflow to Produce and Isolate Natural Killer Cell-derived Extracellular Vesicle-based Cancer Biotherapeutics.

查看英文原题

Scalable Biomanufacturing Workflow to Produce and Isolate Natural Killer Cell-derived Extracellular Vesicle-based Cancer Biotherapeutics.

PubMed 2024/08/16(内容时间) J Vis Exp Q3 · IF 1.2(JCR 2025)

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中文摘要

NK 细胞来源的细胞外囊泡(NK-EVs)正被研究作为癌症生物治疗药物。它们具有独特的特性,既可作为靶向癌细胞的细胞毒性纳米囊泡,也可作为免疫调节通讯者。可规模化的生物制造工作流程能够生产大量高纯度的NK-EVs,以满足临床前和临床需求。该工作流程采用闭环中空纤维生物反应器,能够在无血清、无异种成分、无饲养层和无抗生素的条件下,从NK92-MI细胞系连续生产NK-EVs,并符合药品生产质量管理规范标准。这项方案驱动的研究概述了使用尺寸排阻色谱、超滤和基于滤器的灭菌来分离NK-EVs的生物制造工作流程。通过纳米颗粒追踪分析进行必要的NK-EV产品表征,并通过经过验证的基于细胞活力的针对癌细胞的效力测定来评估其功能性。这一可规模化的生物制造工艺通过遵循最佳实践并确保可重复性,具有推动基于NK-EV的癌症生物治疗药物临床转化的巨大潜力。

展开英文摘要原文

Natural killer cell-derived extracellular vesicles (NK-EVs) are being investigated as cancer biotherapeutics. They possess unique properties as cytotoxic nanovesicles targeting cancer cells and as immunomodulatory communicators. A scalable biomanufacturing workflow enables the production of large quantities of high-purity NK-EVs to meet the pre-clinical and clinical demands. The workflow employs a closed-loop hollow-fiber bioreactor, enabling continuous production of NK-EVs from the NK92-MI cell line under serum-free, xeno-free, feeder-free, and antibiotic-free conditions in compliance with Good Manufacturing Practices standards.

This protocol-driven study outlines the biomanufacturing workflow for isolating NK-EVs using size-exclusion chromatography, ultrafiltration, and filter-based sterilization. Essential NK-EV product characterization is performed via nanoparticle tracking analysis, and their functionality is assessed through a validated cell viability-based potency assay against cancer cells.

This scalable biomanufacturing process holds significant potential to advance the clinical translation of NK-EV-based cancer biotherapeutics by adhering to best practices and ensuring reproducibility.

论文信息

作者
St-Denis-Bissonnette F、Kirkby M、Wang L、Lavoie JR
第一作者单位
Biologic and Radiopharmaceutical Drugs Directorate; Department of Biochemistry, Microbiology and Immunology Institute, University of Ottawa.Canada
通讯作者单位
Biologic and Radiopharmaceutical Drugs Directorate; Department of Biochemistry, Microbiology and Immunology Institute, University of Ottawa; jessie.lavoie@hc-sc.gc.ca.Canada
文献类型
音视频资料 · 非美国政府资助研究
期刊
Journal of visualized experiments : JoVE2024 Aug 16
原文标识
PubMed 39221940 · DOI 10.3791/67227