Effect of refeed strategies and non-ammoniagenic medium on adenovirus production at high cell densities

被引:44
作者
Ferreira, TB
Ferreira, AL
Carrondo, MJT
Alves, PM
机构
[1] Inst Tecnol Quim & Biol, Inst Biol Expt & Tecnol, P-2781901 Oeiras, Portugal
[2] Univ Nova Lisboa, Engn Bioquim Lab, Fac Ciencias & Tecnol, P-2825114 Monte De Caparica, Portugal
关键词
adenovirus; high cell densities; refeed; non-ammoniagenic medium;
D O I
10.1016/j.jbiotec.2005.03.009
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Recombinant adenoviruses became one of the vectors of choice for delivery and expression of foreign proteins for gene therapy and vaccination purposes. Nevertheless, the production of adenovirus is currently limited by the so-called "cell density effect", i.e., a drop in cell specific productivity concomitant with increased cell concentration at infection (CCI). This work describes the characterisation and optimisation of the infection process in order to improve recombinant adenovirus type 5 yields at high cell densities. For that purpose, 293 cells adapted to suspension were grown in 21 bioreactors and infected at different cell concentrations, using different refeed strategies, while evaluating cell metabolism. The consumption of amino acids is enhanced during infection, although no amino acid limitation was detected for cells infected at concentrations in the range of 2 X 10(6) cell/ml, for which the highest volumetric productivity was obtained in batch mode. Conversely, infecting at cell concentrations in the range of 3 x 10(6) cell/ml led to complete depletion of glucose, glutamine and threonine before the optimal harvesting time, a significant decrease in volumetric productivity being observed; the effect of amino acids and glucose addition at infection time on cell specific and volumetric productivity of adenovirus was assessed, no improvement on adenovirus production being achieved. The effect of ammonia, present in high concentrations at 3 x 10(6) cell/ml, was evaluated and seem to be detrimental; an 1.8-fold increase on adenovirus volumetric productivity was obtained for infections performed at 3 x 10(6) cell/ml when non-ammoniagenic medium was used. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:272 / 280
页数:9
相关论文
共 25 条
[11]   PURIFICATION OF A TYPE-5 RECOMBINANT ADENOVIRUS ENCODING HUMAN P53 BY COLUMN CHROMATOGRAPHY [J].
HUYGHE, BG ;
LIU, XD ;
SUTJIPTO, S ;
SUGARMAN, BJ ;
HORN, MT ;
SHEPARD, HM ;
SCANDELLA, CJ ;
SHABRAM, P .
HUMAN GENE THERAPY, 1995, 6 (11) :1403-1416
[12]   Comparison of manufacturing techniques for adenovirus production [J].
Iyer, P ;
Ostrove, JM ;
Vacante, D .
CYTOTECHNOLOGY, 1999, 30 (1-3) :169-172
[13]   pH, pCO2, and temperature effect on R-adenovirus production [J].
Jardon, M ;
Garnier, A .
BIOTECHNOLOGY PROGRESS, 2003, 19 (01) :202-208
[14]   Development and optimization of an adenovirus production process [J].
Kamen, A ;
Henry, O .
JOURNAL OF GENE MEDICINE, 2004, 6 :S184-S192
[15]  
MATSUDAIRA P, 1990, METHODS ENZYMOLOGY
[16]  
MCQUEEN A, 1991, BIOPROCESS ENG, V6, P49
[17]   Gene therapy: the first decade [J].
Mountain, A .
TRENDS IN BIOTECHNOLOGY, 2000, 18 (03) :119-128
[18]  
Nadeau I, 1996, BIOTECHNOL BIOENG, V51, P613, DOI 10.1002/(SICI)1097-0290(19960920)51:6<613::AID-BIT1>3.0.CO
[19]  
2-K
[20]   Production of adenovirus vector for gene therapy [J].
Nadeau, I ;
Kamen, A .
BIOTECHNOLOGY ADVANCES, 2003, 20 (7-8) :475-489