发明公开
EP0832980A1 Recombinant therapies for infection and hyperproliferative disorders
失效
用于感染和过度增殖性疾病的重组疗法
- 专利标题: Recombinant therapies for infection and hyperproliferative disorders
- 专利标题(中): 用于感染和过度增殖性疾病的重组疗法
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申请号: EP97113730.2申请日: 1990-01-22
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公开(公告)号: EP0832980A1公开(公告)日: 1998-04-01
- 发明人: Goldsmith, Mark A. , Ralston, Robert O.
- 申请人: CHIRON CORPORATION
- 申请人地址: 4560 Horton Street Emeryville, California 94608 US
- 专利权人: CHIRON CORPORATION
- 当前专利权人: CHIRON CORPORATION
- 当前专利权人地址: 4560 Horton Street Emeryville, California 94608 US
- 代理机构: Irvine, Jonquil Claire
- 优先权: US300637 19890123; US461461 19900117
- 主分类号: C12N15/85
- IPC分类号: C12N15/85 ; A61K39/12 ; C07H15/12 ; C12N15/00 ; C12N5/10 ; C12N7/00 ; A61K48/00
摘要:
The present invention provides polynucleotide constructs, e.g. recombinant viral vectors, for treating a host cell for a hyperproliferative disorder or infection by an infectious agent, said infection or hyperproliferative disorder being characterised by a human disease-associated trans-acting regulatory factor capable of regulating expression of genes. In particular, the present invention provides such constructs comprising:
(i) at least two tandem copies of a cis-acting regulatory sequence which are controllable by said trans-acting regulatory factor; and
(ii) an effector gene under the control of said cis-acting regulatory sequence the expression of which renders said cell susceptible to protection or destruction, said effector gene encoding a gene product which is capable of converting a prodrug into its active drug form.
(i) at least two tandem copies of a cis-acting regulatory sequence which are controllable by said trans-acting regulatory factor; and
(ii) an effector gene under the control of said cis-acting regulatory sequence the expression of which renders said cell susceptible to protection or destruction, said effector gene encoding a gene product which is capable of converting a prodrug into its active drug form.
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