VECTEURS ADENOVIRAUX RECOMBINANTS COMPRENANT UNE SEQUENCE D'EPISSAGE
    4.
    发明公开
    VECTEURS ADENOVIRAUX RECOMBINANTS COMPRENANT UNE SEQUENCE D'EPISSAGE 失效
    重组腺病毒载体甲SPLEISSEQUENZ CONTAIN

    公开(公告)号:EP0988391A2

    公开(公告)日:2000-03-29

    申请号:EP98928412.0

    申请日:1998-06-02

    申请人: TRANSGENE S.A.

    摘要: The invention concerns a recombinant adenoviral vector driving from an adenovirus genome at least by deleting all or part of the E1 region, said adenoviral vector comprising an expression cassette of a gene of interest placed under the control of elements necessary for its expression in a host cell or a host organism, said elements required for its expression including at least a splicing sequence. The invention is characterised in that said splicing sequence is derived from a eukaryotic nuclear gene selected among the ovalbumen genes, α or β-globine, collagen and factor VIII of mammals or a synthetic splicing sequence. The invention also concerns a host cell and an infectious viral particle comprising such a vector, a method for preparing such a particle and their therapeutic or prophylactic use. The invention further concerns a pharmaceutical composition containing said adenoviral vector, said host cell or said viral particle.

    VECTEURS ADENOVIRAUX RECOMBINANTS COMPRENANT UNE SEQUENCE D'EPISSAGE
    5.
    发明授权
    VECTEURS ADENOVIRAUX RECOMBINANTS COMPRENANT UNE SEQUENCE D'EPISSAGE 失效
    重组腺病毒载体甲SPLEISSEQUENZ CONTAIN

    公开(公告)号:EP0988391B1

    公开(公告)日:2004-12-15

    申请号:EP98928412.0

    申请日:1998-06-02

    申请人: TRANSGENE S.A.

    摘要: The invention concerns a recombinant adenoviral vector driving from an adenovirus genome at least by deleting all or part of the E1 region, said adenoviral vector comprising an expression cassette of a gene of interest placed under the control of elements necessary for its expression in a host cell or a host organism, said elements required for its expression including at least a splicing sequence. The invention is characterised in that said splicing sequence is derived from a eukaryotic nuclear gene selected among the ovalbumen genes, α or β-globine, collagen and factor VIII of mammals or a synthetic splicing sequence. The invention also concerns a host cell and an infectious viral particle comprising such a vector, a method for preparing such a particle and their therapeutic or prophylactic use. The invention further concerns a pharmaceutical composition containing said adenoviral vector, said host cell or said viral particle.