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采用挤压技术符合药品生产质量管理规范(GMP)的生物活性细胞衍生囊泡的生产

GMP-compliant manufacturing of biologically active cell-derived vesicles produced by extrusion technology.

作者信息

Lau Hui-Chong, Han Dong Woo, Park Jinhee, Lehner Edwine, Kals Carina, Arzt Claudia, Bayer Elisabeth, Auer Daniela, Schally Tanja, Grasmann Eva, Fang Han, Lee Jae-Young, Lee Hyun Soo, Han Jinah, Gimona Mario, Rohde Eva, Bae Shingyu, Oh Seung Wook

机构信息

BioDrone Research Institute MDimune Inc. Seoul Korea.

GMP Unit, Spinal Cord Injury & Tissue Regeneration Centre Salzburg (SCI-TReCS) Paracelsus Medical University Salzburg Austria.

出版信息

J Extracell Biol. 2022 Dec 25;1(12):e70. doi: 10.1002/jex2.70. eCollection 2022 Dec.

DOI:10.1002/jex2.70
PMID:38938599
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11080851/
Abstract

Extracellular vesicles (EVs) released by a variety of cell types have been shown to act as a natural delivery system for bioactive molecules such as RNAs and proteins. EV therapy holds great promise as a safe and cell-free therapy for many immunological and degenerative diseases. However, translation to clinical application is limited by several factors, including insufficient large-scale manufacturing technologies and low yield. We have developed a novel drug delivery platform technology, BioDrone™, based on cell-derived vesicles (CDVs) produced from diverse cell sources by using a proprietary extrusion process. This extrusion technology generates nanosized vesicles in far greater numbers than naturally obtained EVs. We demonstrate that the CDVs are surrounded by a lipid bilayer membrane with a correct membrane topology. Physical, biochemical and functional characterisation results demonstrate the potential of CDVs to act as effective therapeutics. Umbilical cord mesenchymal stem cell (UCMSC)-derived CDVs exhibit a biological activity that is similar to UCMSCs or UCMSC-derived EVs. Lastly, we present the establishment of a GMP-compliant process to allow the production of a large number of UCMSC-CDVs in a reproducible manner. GMP-compliant manufacturing of CDVs will facilitate the preclinical and clinical evaluation of these emerging therapeutics in anti-inflammatory or regenerative medicine. This study also represents a crucial step in the development of this novel drug delivery platform based on CDVs.

摘要

多种细胞类型释放的细胞外囊泡(EVs)已被证明可作为RNA和蛋白质等生物活性分子的天然递送系统。EV疗法作为一种针对多种免疫和退行性疾病的安全且无细胞的疗法,具有巨大的潜力。然而,向临床应用的转化受到多种因素的限制,包括大规模制造技术不足和产量低。我们基于通过专有挤压工艺从不同细胞来源产生的细胞衍生囊泡(CDVs),开发了一种新型药物递送平台技术BioDrone™。这种挤压技术产生的纳米级囊泡数量比天然获得的EVs多得多。我们证明CDVs被具有正确膜拓扑结构的脂质双分子层膜包围。物理、生化和功能表征结果证明了CDVs作为有效治疗剂的潜力。脐带间充质干细胞(UCMSC)衍生的CDVs表现出与UCMSCs或UCMSC衍生的EVs相似的生物活性。最后,我们展示了建立符合GMP的工艺,以允许以可重复的方式生产大量UCMSC - CDV。符合GMP的CDV制造将促进这些新兴治疗剂在抗炎或再生医学中的临床前和临床评估。这项研究也是基于CDVs的这种新型药物递送平台开发中的关键一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e153/11080851/5dea7502dc17/JEX2-1-e70-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e153/11080851/69b0109fcd9a/JEX2-1-e70-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e153/11080851/b5dad0532035/JEX2-1-e70-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e153/11080851/33ed3651460e/JEX2-1-e70-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e153/11080851/9c5fd8898847/JEX2-1-e70-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e153/11080851/5dea7502dc17/JEX2-1-e70-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e153/11080851/69b0109fcd9a/JEX2-1-e70-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e153/11080851/b5dad0532035/JEX2-1-e70-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e153/11080851/33ed3651460e/JEX2-1-e70-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e153/11080851/9c5fd8898847/JEX2-1-e70-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e153/11080851/5dea7502dc17/JEX2-1-e70-g001.jpg

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