Lentiviral-mediated growth factor gene therapy for neurodegenerative diseases
    3.
    发明授权
    Lentiviral-mediated growth factor gene therapy for neurodegenerative diseases 失效
    慢病毒介导的神经变性疾病生长因子基因治疗

    公开(公告)号:US06800281B2

    公开(公告)日:2004-10-05

    申请号:US10008610

    申请日:2001-11-08

    CPC classification number: C12N15/86 A61K48/00 C07K14/4756 C12N2740/15043

    Abstract: Disclosed and claimed are methods for treating or preventing neurodegenerative diseases, conditions or maladies or symptoms or physiology associated therewith, such as treating or preventing Parkinson's disease or symptoms or physiology associated therewith such as motor deficits or nigrostriatal degeneration; or, for inducing nigrostriatal regeneration. Advantageously, the methods involve administering a lentiviral vector that expresses GDNF, such as human GDNF, or a variant, homolog, analog or derivative thereof.

    Abstract translation: 公开并要求保护的是用于治疗或预防神经变性疾病,病症或疾病或症状或与之相关的生理学的方法,例如治疗或预防帕金森病或与之相关的症状或生理学,例如运动缺陷或黑质纹状体变性; 或用于诱导黑质纹状体再生。 有利地,所述方法包括施用表达GDNF的慢病毒载体,例如人GDNF,或其变体,同系物,类似物或衍生物。

    Retroviral vectors
    4.
    发明授权
    Retroviral vectors 有权
    逆转录病毒载体

    公开(公告)号:US06312682B1

    公开(公告)日:2001-11-06

    申请号:US09224014

    申请日:1998-12-28

    CPC classification number: C12N15/86 A61K48/00 C12N2740/16043 C12N2740/16052

    Abstract: Retroviral vector production systems for producing lentivirus-based vector particles which are capable of infecting and transducing non-dividing target cells, wherein one or more of the auxiliary genes such as vpr, vif, tat, and nef in the case of HIV-1 are absent from the system. The systems and resulting retrovirus vector particles have improved safety over existing systems and vectors.

    Abstract translation: 用于产生能够感染和转导不分裂靶细胞的慢病毒载体颗粒的逆转录病毒载体生产系统,其中在HIV-1的情况下,一种或多种辅助基因如vpr,vif,tat和nef是 缺席系统。 系统和产生的逆转录病毒载体颗粒具有比现有系统和载体更好的安全性。

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