Large-scale processing of recombinant retroviruses for gene therapy

被引:69
作者
Andreadis, ST
Roth, CM
Le Doux, JM
Morgan, JR
Yarmush, ML
机构
[1] Harvard Univ, Ctr Engn Med, Sch Med, Massachusetts Gen Hosp, Boston, MA 02114 USA
[2] Harvard Univ, Surg Serv, Sch Med, Massachusetts Gen Hosp, Boston, MA 02114 USA
[3] Shriners Burns Hosp, Boston, MA 02114 USA
关键词
D O I
10.1021/bp980106m
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
Gene therapy is a new therapeutic modality with the potential of treating inherited and acquired diseases. Several viral and physicochemical vehicles have been used for the transfer of genes to mammalian cells, but recombinant retroviruses are used in the majority of gene therapy clinical trials today. In this communication, we review the major concerns associated with the large-scale production and processing of retroviral particles. While some of the current processes for manufacturing recombinant proteins will be applicable to recombinant retroviruses, the instability, sensitivity to inhibitors, complexity, and size of retroviral particles require that new technologies be designed and evaluated. Here, we examine those issues critical to the design of strategies for production, concentration, and purification as well as formulation and storage of recombinant retroviruses. Processes for large-scale manufacturing of recombinant retroviruses that can produce high gene transfer efficiencies will have significant impact on the clinical implementation of gene therapy.
引用
收藏
页码:1 / 11
页数:11
相关论文
共 85 条
[1]   RAPID PURIFICATION OF EXTRACELLULAR AND INTRACELLULAR MOLONEY MURINE LEUKEMIA-VIRUS [J].
ABOUD, M ;
WOLFSON, M ;
HASSAN, Y ;
HULEIHEL, M .
ARCHIVES OF VIROLOGY, 1982, 71 (03) :185-195
[2]   HUMAN GENE-THERAPY [J].
ANDERSON, WF .
SCIENCE, 1992, 256 (5058) :808-813
[3]   Kinetics of retrovirus mediated gene transfer: The importance of intracellular half-life of retroviruses [J].
Andreadis, ST ;
Palsson, BO .
JOURNAL OF THEORETICAL BIOLOGY, 1996, 182 (01) :1-20
[4]   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
[5]  
[Anonymous], 1996, B MED ETHICS
[6]  
[Anonymous], 1978, General Virology
[7]   Stabilization of active recombinant retroviruses in an amorphous dry state with trehalose [J].
Bieganski, RM ;
Fowler, A ;
Morgan, JR ;
Toner, M .
BIOTECHNOLOGY PROGRESS, 1998, 14 (04) :615-620
[8]   CONVECTION-ENHANCED DELIVERY OF MACROMOLECULES IN THE BRAIN [J].
BOBO, RH ;
LASKE, DW ;
AKBASAK, A ;
MORRISON, PF ;
DEDRICK, RL ;
OLDFIELD, EH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (06) :2076-2080
[9]  
Braas G, 1996, BIOSEPARATION, V6, P211
[10]   VESICULAR STOMATITIS-VIRUS G GLYCOPROTEIN PSEUDOTYPED RETROVIRAL VECTORS - CONCENTRATION TO VERY HIGH-TITER AND EFFICIENT GENE-TRANSFER INTO MAMMALIAN AND NONMAMMALIAN CELLS [J].
BURNS, JC ;
FRIEDMANN, T ;
DRIEVER, W ;
BURRASCANO, M ;
YEE, JK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (17) :8033-8037