Adrien Soula, Florian Leseigneur, Amna Anwar, Bilal Ozdoganoglu, Jagan Gurung, Hamza Bhatti, Juline Guenat, Quentin Bazot, Majahar Sayed, Carolina Pinto Ricardo, Lily Li, Katerina Farukshina, Tony Bou Kheir, Hadi Mirmalek-Sani, Gregory Berger, Julie Kerby, Jonathan Appleby, Michael Delahaye
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In this system, Human Embryonic Kidney 293T cells were successfully expanded and transfected to produce an average crude AAV2 titer of 4.92 × 10<sup>14</sup> viral particles and 6.81 × 10<sup>13</sup> viral genomes from 1.2 L of harvested cell lysate. The application of a standard AAV downstream process confirmed normal processability of the material. A cost of goods model comparing the Quantum bioreactor with the current standard HYPERStack36 and Corning CellSTACK 10-layer systems demonstrated that the Quantum bioreactor reduced the number of open steps by more than 40-fold, production time by up to 3.6-fold (HYPERStack36) and 7.5-fold (CellSTACK 10-layer), and costs by up to 2-fold (HYPERStack36) and 20.7-fold (CellSTACK 10-layer). Therefore, the Quantum bioreactor is an effective alternative to plastic flasks for the manufacturing of AAVs at both R&D and early translational scale, as it reduces production time, operating costs, and process risk.</p>","PeriodicalId":54333,"journal":{"name":"Molecular Therapy-Methods & Clinical Development","volume":"33 2","pages":"101496"},"PeriodicalIF":4.6000,"publicationDate":"2025-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12167053/pdf/","citationCount":"0","resultStr":"{\"title\":\"The manufacture of AAV for gene therapy applications using a closed, semi-automated hollow-fiber bioreactor.\",\"authors\":\"Adrien Soula, Florian Leseigneur, Amna Anwar, Bilal Ozdoganoglu, Jagan Gurung, Hamza Bhatti, Juline Guenat, Quentin Bazot, Majahar Sayed, Carolina Pinto Ricardo, Lily Li, Katerina Farukshina, Tony Bou Kheir, Hadi Mirmalek-Sani, Gregory Berger, Julie Kerby, Jonathan Appleby, Michael Delahaye\",\"doi\":\"10.1016/j.omtm.2025.101496\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Adeno-associated viral (AAV) vectors have been established as a safe and effective delivery vehicle for gene therapy. 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The manufacture of AAV for gene therapy applications using a closed, semi-automated hollow-fiber bioreactor.
Adeno-associated viral (AAV) vectors have been established as a safe and effective delivery vehicle for gene therapy. However, current methods for AAV production using adherent approaches are suboptimal due to their reliance on a substantial number of plastic-based flasks, manual labor, and a significant manufacturing footprint. Consequently, a protocol for generating AAV2 was developed on the Quantum, a semi-automated closed hollow-fiber bioreactor platform. In this system, Human Embryonic Kidney 293T cells were successfully expanded and transfected to produce an average crude AAV2 titer of 4.92 × 1014 viral particles and 6.81 × 1013 viral genomes from 1.2 L of harvested cell lysate. The application of a standard AAV downstream process confirmed normal processability of the material. A cost of goods model comparing the Quantum bioreactor with the current standard HYPERStack36 and Corning CellSTACK 10-layer systems demonstrated that the Quantum bioreactor reduced the number of open steps by more than 40-fold, production time by up to 3.6-fold (HYPERStack36) and 7.5-fold (CellSTACK 10-layer), and costs by up to 2-fold (HYPERStack36) and 20.7-fold (CellSTACK 10-layer). Therefore, the Quantum bioreactor is an effective alternative to plastic flasks for the manufacturing of AAVs at both R&D and early translational scale, as it reduces production time, operating costs, and process risk.
期刊介绍:
The aim of Molecular Therapy—Methods & Clinical Development is to build upon the success of Molecular Therapy in publishing important peer-reviewed methods and procedures, as well as translational advances in the broad array of fields under the molecular therapy umbrella.
Topics of particular interest within the journal''s scope include:
Gene vector engineering and production,
Methods for targeted genome editing and engineering,
Methods and technology development for cell reprogramming and directed differentiation of pluripotent cells,
Methods for gene and cell vector delivery,
Development of biomaterials and nanoparticles for applications in gene and cell therapy and regenerative medicine,
Analysis of gene and cell vector biodistribution and tracking,
Pharmacology/toxicology studies of new and next-generation vectors,
Methods for cell isolation, engineering, culture, expansion, and transplantation,
Cell processing, storage, and banking for therapeutic application,
Preclinical and QC/QA assay development,
Translational and clinical scale-up and Good Manufacturing procedures and process development,
Clinical protocol development,
Computational and bioinformatic methods for analysis, modeling, or visualization of biological data,
Negotiating the regulatory approval process and obtaining such approval for clinical trials.