Premium
Improving adeno‐associated vector yield in high density insect cell cultures
Author(s) -
Mena Jimmy A.,
Aucoin Marc G.,
Montes Johnny,
Chahal Parminder S.,
Kamen Amine A.
Publication year - 2010
Publication title -
the journal of gene medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.689
H-Index - 91
eISSN - 1521-2254
pISSN - 1099-498X
DOI - 10.1002/jgm.1420
Subject(s) - multiplicity of infection , bioreactor , titer , yield (engineering) , recombinant dna , cell culture , baculoviridae , genetic enhancement , viral vector , biology , virology , transduction (biophysics) , adeno associated virus , vector (molecular biology) , virus , gene , materials science , biochemistry , genetics , spodoptera , botany , metallurgy
Background Recombinant adeno‐associated virus (rAAV) are the most promising vectors for gene therapy. However, large‐scale rAAV production remains a challenge for the translation of rAAV‐based therapeutic strategies to the clinic. The baculovirus expression vector system (BEVS) has been engineered to produce high rAAV titers in serum‐free suspension cultures of insect cells. Methods The typical approach of rAAV production in BEVS has been based on a synchronous infection with three baculoviruses at high multiplicity of infection (MOI) [>3 plaque forming units (pfu)/cell]. An alternative approach is to co‐infect at low MOI (0.1 pfu/cell). Both strategies (high and low MOI) were compared at a cell density of 1.0 × 10 6 cells/ml in shake‐flask experiments. To increase the rAAV titer, a low MOI combined with an initial cell density at infection of 5.0 × 10 6 cells/ml, in fed‐batch mode, was evaluated. Subsequently, the production strategy was validated in 3‐l bioreactor runs. Results An increase of 210% in the rAAV titer (4.7 × 10 11 enhanced transduction units/l) was observed when using low MOI, an effect primarily caused by the increase in cell density. The fed‐batch approach resulted in a seven‐fold increase of rAAV yield. Controlled operations in bioreactor contributed to further increase the rAAV yield (2.8 × 10 14 vector genomes/l) by 25% in comparison to the shake flask results. Conclusions This high yield production process using low MOIs and a feeding strategy successfully addresses several limitations of current rAAV production in insect cells and contributes to position the BEVS system as one of the most efficient for large‐scale manufacturing of rAAV vectors. Copyright © 2010 John Wiley & Sons, Ltd. The copyright in Jimmy A. Mena's, Johnny Montes', Parminder S. Chahal's and Amine A. Kamen's contributions belongs to the Crown in right of Canada and such copyright material is reproduced with the permission of the Research Council of Canada.