Improved titers of retroviral vectors from the human FLYRD18 packaging cell line in serum- and protein-free medium

被引:26
作者
Gerin, PA
Gilligan, MG
Searle, PF
Al-Rubeai, M [1 ]
机构
[1] Univ Birmingham, Sch Chem Engn, Birmingham B15 2TT, W Midlands, England
[2] Univ Birmingham, Inst Canc Studies, Birmingham B15 2TT, W Midlands, England
关键词
D O I
10.1089/10430349950017329
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
The influence of serum on the production of retroviral vectors by the HT1080 human fibrosarcoma-derived packaging cell line FLYRD18 was investigated. A fourfold increase in virus titer was observed under serum-free conditions, as compared with medium supplemented with 10% fetal calf serum. A similar improvement was also seen for bulk transduction efficiency. Serum had a negative and dose-dependent effect on titer without affecting cell growth, virus stability, or infectivity, In contrast to virus from NIH 3T3-derived packaging cells [Hanenberg, H., et al, (1996), Nature Med, 2, 876-882], the FLPRD18-derived virus did not adhere to fibronectin or serum proteins adsorbed at the surface of culture flasks. Electron microscopy supports the conclusion that the effect of serum is at the level of virus production by the cells, Addition of soybean trypsin inhibitor had an inhibitory effect on virus production, while pretreatment of serum with trypsin was found to enhance the retroviral titer, These results suggest that protease inhibitors present in serum may be responsible for the inhibition of virus production. The exact mechanism remains, however, to be determined. As compared with medium supplemented with 10% serum, the combination of increased virus titer and absence of exogenous protein under serum-free conditions resulted in a 300-fold increase in the virus:total protein ratio in the supernatants harvested from the FLYRD18 packaging line. This improvement enhances prospects for further concentration and purification of the virus.
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页码:1965 / 1974
页数:10
相关论文
共 25 条
[1]   Coupled effects of polybrene and calf serum on the efficiency of retroviral transduction and the stability of retroviral vectors [J].
Andreadis, S ;
Palsson, BO .
HUMAN GENE THERAPY, 1997, 8 (03) :285-291
[2]   Moloney murine leukemia virus-derived retroviral vectors decay intracellularly with a half-life in the range of 5.5 to 7.5 hours [J].
Andreadis, ST ;
Brott, D ;
Fuller, AO ;
Palsson, BO .
JOURNAL OF VIROLOGY, 1997, 71 (10) :7541-7548
[3]  
[Anonymous], 1990, Fields Virology
[4]  
BEYNON RJ, 1990, PROTEOLYTIC ENZYMES, P241
[5]  
CARTWRIGHT T, 1994, BASIC CELL CULTURE P, P57
[6]  
Choi JH, 1997, BIOPROCESS ENG, V17, P349
[7]   HIGH-TITER PACKAGING CELLS PRODUCING RECOMBINANT RETROVIRUSES RESISTANT TO HUMAN SERUM [J].
COSSET, FL ;
TAKEUCHI, Y ;
BATTINI, JL ;
WEISS, RA ;
COLLINS, MKL .
JOURNAL OF VIROLOGY, 1995, 69 (12) :7430-7436
[8]  
FREEMAN GJ, 1989, J IMMUNOL, V143, P2714
[9]   Adenoviral delivery of B7-1 (CD80) increases the immunogenicity of human ovarian and cervical carcinoma cells [J].
Gilligan, MG ;
Knox, P ;
Weedon, S ;
Barton, R ;
Kerr, DJ ;
Searle, P ;
Young, LS .
GENE THERAPY, 1998, 5 (07) :965-974
[10]   Efficient serum-free retroviral gene transfer into primitive human hematopoietic progenitor cells by a defined, high-titer, nonconcentrated vector-containing medium [J].
Glimm, H ;
Flügge, K ;
Möbest, D ;
Hofmann, VM ;
Postmus, J ;
Henschler, R ;
Lange, W ;
Finke, J ;
Kiem, HP ;
Schulz, G ;
Rosenthal, F ;
Mertelsmann, R ;
von Kalle, C .
HUMAN GENE THERAPY, 1998, 9 (06) :771-778