Monoclonal antibodies produced by muscle after plasmid injection and electroporation

被引:55
|
作者
Tjelle, TE
Corthay, A
Lunde, E
Sandlie, I
Michaelsen, TE
Mathiesen, I
Bogen, B
机构
[1] Inovio AS, N-0373 Oslo, Norway
[2] Univ Oslo, Rikshosp, Inst Immunol, N-0316 Oslo, Norway
[3] Univ Oslo, Dept Biol, N-0316 Oslo, Norway
[4] Norwegian Inst Publ Hlth, Oslo, Norway
[5] Univ Oslo, Inst Pharm, N-0316 Oslo, Norway
关键词
antibody therapy; electroporation; nonviral DNA delivery;
D O I
10.1016/j.ymthe.2003.12.007
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
Antibodies are useful for the treatment of a variety of diseases. We here demonstrate that mouse muscle produced monoclonal antibodies (mAb) after a single injection of immunoglobulin genes as plasmid DNA. In vivo electroporation of muscle greatly enhanced antibody production. For chimeric antibodies, levels of 50-200 ng mAb/ml serum were obtained but levels declined after 7-14 days due to an immune response against the xenogeneic parts of the antibody. By contrast, fully mouse antibodies persisted in serum for at least 7 months. mAb produced by the muscle had correct structure, specificity, and biological effector functions. The findings were extended to a larger animal, the sheep, in which mAb serum levels of 30-50 ng/ml were obtained. Sustained levels of serum mAb, induced by single injection of Ig genes and electroporation of muscle cells, may offer significant advantages in the treatment of human diseases.
引用
收藏
页码:328 / 336
页数:9
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