Development and characterization of a cell line for large-scale, serum-free production of recombinant adeno-associated viral vectors
- PMID: 15538729
- DOI: 10.1002/jgm.622
Development and characterization of a cell line for large-scale, serum-free production of recombinant adeno-associated viral vectors
Abstract
Background: One of the major limitations to the use of adeno-associated virus (AAV) vectors for gene therapy has been the difficulty in producing enough vector to supply a clinical trial. More than 20 000 roller bottles may be required to generate AAV by the traditional transient transfection process to treat 50 patients. A scalable AAV producer cell line grown in serum-free media will meet the needs for the manufacture of AAV gene therapeutics.
Methods: A packaging cell line was generated by introducing the AAV rep and cap genes into A549 cells. From this packaging cell line, a number of producer cell lines were generated by infecting the packaging cell with the appropriate AAV vector. Producer cell lines were then adapted to serum-free suspension conditions for growth in bioreactors.
Results: We report here the development of six AAV producer cell lines that generate > 10(4) particles/cell. The rAAV vector preparations from these cell lines have physical and functional characteristics similar to rAAV vectors prepared by transient transfection. To enable large-scale production, producer cell lines were adapted to serum-free suspension and we demonstrate production of AAV at the 15 L scale. In addition, vector preparations from these cell lines were shown to be free of wild-type AAV.
Conclusions: AAV producer cell lines can be readily scaled to meet the needs of clinical trials. One 500 L bioreactor of these producer cells can produce the equivalent of 2500 high capacity roller bottles or 25 000 T-175 tissue culture flasks.
Copyright 2004 John Wiley & Sons, Ltd.
Similar articles
-
High-titer recombinant adeno-associated virus production utilizing a recombinant herpes simplex virus type I vector expressing AAV-2 Rep and Cap.Gene Ther. 1999 Jun;6(6):986-93. doi: 10.1038/sj.gt.3300937. Gene Ther. 1999. PMID: 10455400
-
Scalable serum-free production of recombinant adeno-associated virus type 2 by transfection of 293 suspension cells.J Virol Methods. 2007 Sep;144(1-2):32-40. doi: 10.1016/j.jviromet.2007.03.014. Epub 2007 Apr 30. J Virol Methods. 2007. PMID: 17467815
-
Production of recombinant adeno-associated virus vectors using a packaging cell line and a hybrid recombinant adenovirus.Gene Ther. 1999 Feb;6(2):293-9. doi: 10.1038/sj.gt.3300807. Gene Ther. 1999. PMID: 10435114
-
Development and optimization of an adenovirus production process.J Gene Med. 2004 Feb;6 Suppl 1:S184-92. doi: 10.1002/jgm.503. J Gene Med. 2004. PMID: 14978761 Review.
-
Adeno-associated virus as a gene therapy vector: vector development, production and clinical applications.Adv Biochem Eng Biotechnol. 2005;99:119-45. Adv Biochem Eng Biotechnol. 2005. PMID: 16568890 Review.
Cited by
-
Evaluation of a Serum-free Medium for the Production of rAAV-2 using HeLa Derived Producer Cells.Cytotechnology. 2005 Sep;49(1):11-23. doi: 10.1007/s10616-005-5361-z. Cytotechnology. 2005. PMID: 19003059 Free PMC article.
-
Cell culture processes for the production of viral vectors for gene therapy purposes.Cytotechnology. 2006 Mar;50(1-3):141-62. doi: 10.1007/s10616-005-5507-z. Epub 2006 Jun 30. Cytotechnology. 2006. PMID: 19003076 Free PMC article.
-
AAV production in stable packaging cells requires expression of adenovirus 22/33K protein to allow episomal amplification of integrated rep/cap genes.Sci Rep. 2023 Dec 7;13(1):21670. doi: 10.1038/s41598-023-48901-z. Sci Rep. 2023. PMID: 38066084 Free PMC article.
-
Comparison of highly pure rAAV9 vector stocks produced in suspension by PEI transfection or HSV infection reveals striking quantitative and qualitative differences.Mol Ther Methods Clin Dev. 2021 Dec 25;24:154-170. doi: 10.1016/j.omtm.2021.12.006. eCollection 2022 Mar 10. Mol Ther Methods Clin Dev. 2021. PMID: 35071688 Free PMC article.
-
Producing recombinant adeno-associated virus in foster cells: overcoming production limitations using a baculovirus-insect cell expression strategy.Hum Gene Ther. 2009 Aug;20(8):807-17. doi: 10.1089/hum.2009.092. Hum Gene Ther. 2009. PMID: 19604040 Free PMC article. Review.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous