Method of targeted gene delivery using viral vectors
    1.
    发明授权
    Method of targeted gene delivery using viral vectors 有权
    使用病毒载体的靶向基因递送方法

    公开(公告)号:US08821856B2

    公开(公告)日:2014-09-02

    申请号:US13041115

    申请日:2011-03-04

    摘要: Methods and compositions are provided for delivering a polynucleotide encoding a gene of interest to a target cell using a virus. The virus envelope comprises a cell-specific binding determinant that recognizes and binds to a component on the target cell surface, leading to endocytosis of the virus. A separate fusogenic molecule is also present on the envelope and facilitates delivery of the polynucleotide across the membrane and into the cytosol of the target cell. The methods and related compositions can be used for treating patients having suffering from a wide range of conditions, including infection, such as HIV; cancers, such as non-Hodgkin's lymphoma and breast cancer; and hematological disorders, such as severe combined immunodeficiency.

    摘要翻译: 提供了使用病毒将编码目标基因的多核苷酸递送至靶细胞的方法和组合物。 病毒包膜包含识别和结合靶细胞表面上的组分的细胞特异性结合决定簇,导致病毒的内吞。 单独的融合分子也存在于包膜上并促进多核苷酸穿过膜并进入靶细胞的胞质溶胶。 方法和相关组合物可用于治疗患有广泛病症(包括HIV感染)的患者; 癌症,如非霍奇金淋巴瘤和乳腺癌; 和血液学疾病,如严重的联合免疫缺陷。

    METHOD OF TARGETED GENE DELIVERY USING VIRAL VECTORS
    6.
    发明申请
    METHOD OF TARGETED GENE DELIVERY USING VIRAL VECTORS 有权
    使用病毒载体的目标基因传递方法

    公开(公告)号:US20110212530A1

    公开(公告)日:2011-09-01

    申请号:US13041115

    申请日:2011-03-04

    IPC分类号: C12N15/63

    摘要: Methods and compositions are provided for delivering a polynucleotide encoding a gene of interest to a target cell using a virus. The virus envelope comprises a cell-specific binding determinant that recognizes and binds to a component on the target cell surface, leading to endocytosis of the virus. A separate fusogenic molecule is also present on the envelope and facilitates delivery of the polynucleotide across the membrane and into the cytosol of the target cell. The methods and related compositions can be used for treating patients having suffering from a wide range of conditions, including infection, such as HIV; cancers, such as non-Hodgkin's lymphoma and breast cancer; and hematological disorders, such as severe combined immunodeficiency.

    摘要翻译: 提供了使用病毒将编码目标基因的多核苷酸递送至靶细胞的方法和组合物。 病毒包膜包含识别和结合靶细胞表面上的组分的细胞特异性结合决定簇,导致病毒的内吞。 单独的融合分子也存在于包膜上并促进多核苷酸穿过膜并进入靶细胞的胞质溶胶。 方法和相关组合物可用于治疗患有广泛病症(包括HIV感染)的患者; 癌症,如非霍奇金淋巴瘤和乳腺癌; 和血液学疾病,如严重的联合免疫缺陷。