TARGETED AND HIGHLY EFFICIENT GENE-TRANSFER INTO CD4+ CELLS BY A RECOMBINANT HUMAN-IMMUNODEFICIENCY-VIRUS RETROVIRAL VECTOR

被引:85
|
作者
SHIMADA, T [1 ]
FUJII, H [1 ]
MITSUYA, H [1 ]
NIENHUIS, AW [1 ]
机构
[1] NCI,CLIN ONCOL PROGRAM,BETHESDA,MD 20892
来源
JOURNAL OF CLINICAL INVESTIGATION | 1991年 / 88卷 / 03期
关键词
GENE TRANSFER; GENE THERAPY; AIDS; INTRACELLULAR IMMUNIZATION; COS CELLS;
D O I
10.1172/JCI115365
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
We have established a recombinant HIV gene transfer system based on transient expression of the HIV packaging functions and a recombinant vector genome in monkey kidney Cos cells. The recombinant HIV retroviral vector introduced the neo(R) gene into CD4+ cells with high efficiency, comparable to that achieved with the highest titer amphotropic murine recombinant retrovirus. Vector preparations were devoid of replication competent, infectious HIV. Gene transfer was dependent on CD4 expression, as shown by expression of the CD4 gene in HeLa cells, and could be inhibited by soluble CD4. This specific and efficient gene transfer system may be useful for development of gene therapy for which T cells are the desired targets.
引用
收藏
页码:1043 / 1047
页数:5
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