A new packaging cell line for SV40 vectors that eliminates the generation of T-antigen-positive, replication-competent recombinants

被引:12
作者
Arad, U
Ben-Nun-Shaul, O
Abd El-Latif, M
Nissim, O
Oppenheim, A
机构
[1] Hadassah Univ Hosp, Dept Hematol, IL-91120 Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Hadassah Med Sch, Dept Hematol, IL-91010 Jerusalem, Israel
基金
以色列科学基金会;
关键词
SV40; gene therapy; packaging cell line; recombination;
D O I
10.1006/viro.2002.1791
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Simian virus 40 (SV40) vectors are efficient vehicles for gene delivery to hematopoietic and hepatic cells. To ensure their replication incompetence and because of safety considerations, it is critical that the vectors do not contain T-antigen sequences. Available packaging cell lines for T-antigen replacement vectors, COS and CMT4, contain considerable sequence identity with the vectors, leading to homologous recombination and reacquisition of the T-antigen gene. We constructed a packaging cell line, COT18, with minimal sequence identity to the vector. Vector stocks produced by passaging on COT18 had high transducing activity and undetectable levels of T-antigen-positive, replication-competent contaminants. This cell line provides a means for the preparation of safe SV40 vector stocks. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:155 / 159
页数:5
相关论文
共 20 条
[1]   Identification and elimination of replication-competent adeno-associated virus (AAV) that can arise by nonhomologous recombination during AAV vector production [J].
Allen, JM ;
Debelak, DJ ;
Reynolds, TC ;
Miller, AD .
JOURNAL OF VIROLOGY, 1997, 71 (09) :6816-6822
[2]   A replication-competent retrovirus arising from a split-function packaging cell line was generated by recombination events between the vector, one of the packaging constructs, and endogenous retroviral sequences [J].
Chong, H ;
Starkey, W ;
Vile, RG .
JOURNAL OF VIROLOGY, 1998, 72 (04) :2663-2670
[3]   Expression of β-globin in primary erythroid progenitors of β-thalassemia patients using an SV40-based gene delivery system [J].
Dalyot-Herman, N ;
Rund, D ;
Oppenheim, A .
JOURNAL OF HEMATOTHERAPY & STEM CELL RESEARCH, 1999, 8 (06) :593-599
[4]   The simian virus 40 packaging signal ses is composed of redundant DNA elements which are partly interchangeable [J].
DalyotHerman, N ;
BennunShaul, O ;
GordonShaag, A ;
Oppenheim, A .
JOURNAL OF MOLECULAR BIOLOGY, 1996, 259 (01) :69-80
[5]   Who's afraid of replication-competent adenoviruses? [J].
Fallaux, FJ ;
van der Eb, AJ ;
Hoeben, RC .
GENE THERAPY, 1999, 6 (05) :709-712
[6]   SV40-TRANSFORMED SIMIAN CELLS SUPPORT THE REPLICATION OF EARLY SV40 MUTANTS [J].
GLUZMAN, Y .
CELL, 1981, 23 (01) :175-182
[7]   HIGH-FREQUENCY OF HOMOLOGOUS RECOMBINATION IN MAMMALIAN-CELLS BETWEEN ENDOGENOUS AND INTRODUCED SV40 GENOMES [J].
JASIN, M ;
DEVILLIERS, J ;
WEBER, F ;
SCHAFFNER, W .
CELL, 1985, 43 (03) :695-703
[8]  
LISKAY RM, 1987, GENETICS, V115, P161
[9]  
MILLER AD, 1989, BIOTECHNIQUES, V7, P980
[10]   HELPERS FOR EFFICIENT ENCAPSIDATION OF SV40 PSEUDOVIRIONS [J].
OPPENHEIM, A ;
PELEG, A .
GENE, 1989, 77 (01) :79-86