Autre titre | New complementing cells for production of E1-deleted adenovirus vectors in serum-free suspension culture |
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Téléchargement | - Voir le manuscrit accepté : Establishment and validation of new complementing cells for production of E1-deleted adenovirus vectors in serum-free suspension culture (PDF, 2.5 Mio)
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DOI | Trouver le DOI : https://doi.org/10.1016/j.jviromet.2014.08.013 |
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Auteur | Rechercher : Gilbert, Rénald1; Rechercher : Guilbault, Claire1; Rechercher : Gagnon, David1; Rechercher : Bernier, Alice1; Rechercher : Bourget, Lucie1; Rechercher : Elahi, Seyyed Mehdy1; Rechercher : Kamen, Amine1; Rechercher : Massie, Bernard1 |
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Affiliation | - Conseil national de recherches du Canada. Thérapeutique en santé humaine
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Format | Texte, Article |
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Sujet | Adenovirus vectors; Suspension culture; Serum-free medium; Cell line; Replication-competent adenovirus |
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Résumé | E1-deleted adenovirus vectors (AdV) are important gene transfer vehicles for gene therapy and vaccination. Amplification of AdV must take place in cells that express the adenovirus E1A and E1B genes. Sequence homology between AdV and the E1 genes integrated within the complementing cells should be minimal to reduce the odds of generating replication-competent adenovirus (RCA). The present study describes the establishment of AdV complementing cells constructed by stable transfection of the minimal E1A and E1B genes into human lung carcinoma (A549). Because some transgene products can be cytotoxic, the cells were engineered to stably express the repressor of the cumate-switch (CymR) to silence transgene transcription during vector growth. For regulatory compliance and to facilitate the scale-up, the resulting complementing cells (SF-BMAdR) were adapted to serum-free suspension culture. The best clone of SF-BMAdR produced AdV carrying an innocuous transgene to the same level as 293 cells, but titers were better for AdV carrying transgene for a cytotoxic product. Elevated titers were maintained for at least two months in suspension culture in the absence of selective agent and the cells did not produce RCA. Because of their advantageous properties, SF-BMAdR cells should become an important tool for developing large-scale production processes of AdV for research and clinical applications. |
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Date de publication | 2014-08-23 |
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Dans | |
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Langue | anglais |
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Publications évaluées par des pairs | Oui |
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Numéro du CNRC | NRC-HHT-53257 |
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Numéro NPARC | 21272877 |
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Exporter la notice | Exporter en format RIS |
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Signaler une correction | Signaler une correction (s'ouvre dans un nouvel onglet) |
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Identificateur de l’enregistrement | 55d1e495-a328-4708-8aee-eee63968a47d |
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Enregistrement créé | 2014-12-03 |
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Enregistrement modifié | 2020-06-04 |
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