Optimized conditions for the production of recombinant amphotropic retroviral vector preparations

被引:40
作者
Kaptein, LCM
Greijer, AE
Valerio, D
vanBeusechem, VW
机构
[1] LEIDEN UNIV,GENE THERAPY SECT,DEPT BIOCHEM MED,NL-2280 GG RIJSWIJK,NETHERLANDS
[2] INTROGENE BV,RIJSWIJK,NETHERLANDS
关键词
retroviral vector titer; retroviral vector stability; gene therapy;
D O I
10.1038/sj.gt.3300373
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The production and stability of recombinant retroviral vectors was examined at various temperatures. The two studied recombinant retroviral vectors, based on different packaging cell lines, exhibited a four-fold increased half-life at 32 degrees C as compared to 37 degrees C. Surprisingly this increased stability, at 32 degrees C was only observed within a very narrow temperature window. At 30 degrees C and 34 degrees C, retroviral vector half-lives were quite similar to that at 37 degrees C. Regardless of the vector half-life, retroviral vectors accumulated in the culture medium for a period of 48 h before an equilibrium was reached between retroviral vector production and decay. Maximal accumulated recombinant retroviral titers were five- to ten-fold increased after a medium incubation, at 32 degrees C as compared to 37 degrees C. Furthermore, multiple cycles of freezing and thawing of retroviral vector supernatants hardly affected the recombinant retroviral vector titer, independent of the presence of serum. This knowledge on characteristics of recombinant retroviral vectors has practical implications for the manufacturing of these viruses for clinical gene therapy protocols.
引用
收藏
页码:172 / 176
页数:5
相关论文
共 17 条
[1]   EFFECT OF INTERNAL VIRAL SEQUENCES ON THE UTILITY OF RETROVIRAL VECTORS [J].
ARMENTANO, D ;
YU, SF ;
KANTOFF, PW ;
VONRUDEN, T ;
ANDERSON, WF ;
GILBOA, E .
JOURNAL OF VIROLOGY, 1987, 61 (05) :1647-1650
[2]   HIGH-EFFICIENCY TRANSFORMATION OF MAMMALIAN-CELLS BY PLASMID DNA [J].
CHEN, C ;
OKAYAMA, H .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (08) :2745-2752
[3]  
CORRELL PH, 1994, BLOOD, V84, P1812
[4]  
Forestell SP, 1995, GENE THER, V2, P723
[5]   IMPROVED METHODS OF RETROVIRAL VECTOR TRANSDUCTION AND PRODUCTION FOR GENE-THERAPY [J].
KOTANI, H ;
NEWTON, PB ;
ZHANG, SY ;
CHIANG, YWL ;
OTTO, E ;
WEAVER, L ;
BLAESE, RM ;
ANDERSON, WF ;
MCGARRITY, GJ .
HUMAN GENE THERAPY, 1994, 5 (01) :19-28
[6]   PING-PONG AMPLIFICATION OF A RETROVIRAL VECTOR ACHIEVES HIGH-LEVEL GENE-EXPRESSION - HUMAN GROWTH-HORMONE PRODUCTION [J].
KOZAK, SL ;
KABAT, D .
JOURNAL OF VIROLOGY, 1990, 64 (07) :3500-3508
[7]   QUANTIFYING THE INFECTIVITY OF HUMAN IMMUNODEFICIENCY VIRUS [J].
LAYNE, SP ;
SPOUGE, JL ;
DEMBO, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (12) :4644-4648
[8]   INCREASE OF RETROVIRAL INFECTION INVITRO BY THE BINDING OF ANTIRETROVIRAL ANTIBODIES [J].
LEGRAIN, P ;
GOUD, B ;
BUTTIN, G .
JOURNAL OF VIROLOGY, 1986, 60 (03) :1141-1144
[9]   PRODUCTION OF HIGH-TITER HELPER VIRUS-FREE RETROVIRAL VECTORS BY COCULTIVATION OF PACKAGING CELLS WITH DIFFERENT HOST RANGES [J].
LYNCH, CM ;
MILLER, AD .
JOURNAL OF VIROLOGY, 1991, 65 (07) :3887-3890
[10]   RETROVIRAL VECTORS CONTAINING PUTATIVE INTERNAL RIBOSOME ENTRY SITES - DEVELOPMENT OF A POLYCISTRONIC GENE-TRANSFER SYSTEM AND APPLICATIONS TO HUMAN GENE-THERAPY [J].
MORGAN, RA ;
COUTURE, L ;
ELROYSTEIN, O ;
RAGHEB, J ;
MOSS, B ;
ANDERSON, WF .
NUCLEIC ACIDS RESEARCH, 1992, 20 (06) :1293-1299