DIRECT GENE-TRANSFER INTO MUSCLE

被引:92
作者
DANKO, I
WOLFF, JA
机构
[1] UNIV WISCONSIN,WAISMAN CTR,DEPT MED GENET,MADISON,WI 53705
[2] UNIV WISCONSIN,WAISMAN CTR,DEPT NEUROL,MADISON,WI 53705
关键词
PLASMID DNA; GENE TRANSFER; GENE EXPRESSION; GENE THERAPY; LUCIFERASE; BETA-GALACTOSIDASE; VACCINATION;
D O I
10.1016/0264-410X(94)90072-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Gene therapy has great promise for the treatment and the prevention of a broad range of inherited and acquired diseases. Gene transfer methods currently explored include the use of viral vectors and physical-chemical methods. Plasmid DNA can be taken up by skeletal muscle cells in vivo without any special delivery mechanism and persist long-term in an extrachromosomal, non-replicative circular form. Thus, foreign genes can be expressed permanently in skeletal muscle. Ar present the efficiency of gene transfer is not high enough to treat genetic muscle diseases. However, even at the relatively low efficiency of expression we are able to achieve at present, plasmid DNA transfer seems to be a very promising way of programming cells in vivo to secrete proteins for immunization purposes.
引用
收藏
页码:1499 / 1502
页数:4
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