Compositions and methods for the abrogation of cellular proliferation utilizing the human immunodeficiency virus VPR protein
    6.
    发明授权
    Compositions and methods for the abrogation of cellular proliferation utilizing the human immunodeficiency virus VPR protein 失效
    使用人类免疫缺陷病毒VPR蛋白消除细胞增殖的组合物和方法

    公开(公告)号:US06667157B1

    公开(公告)日:2003-12-23

    申请号:US08809186

    申请日:1997-06-24

    IPC分类号: G01N33567

    摘要: Method of inhibiting proliferation of cells using vpr protein or nucleotide sequences that encode vpr are disclosed. Method of preventing lymphocyte activation using vpr protein or nucleotide sequences that encode vpr are disclosed. Methods of treating an individual diagnosed with or suspected of suffering from autoimmune disease, diseases characterized by proliferating cells and graft versus host disease by administering vpr protein or a functional fragment thereof, or a nucleic acid molecule that comprises a nucleotide sequence that encodes vpr protein or a functional fragment thereof are disclosed. Conjugated compositions for delivery of active agents to the nucleus of cells are disclosed.

    摘要翻译: 公开了使用vpr蛋白抑制细胞增殖的方法或编码vpr的核苷酸序列。 公开了使用vpr蛋白或编码vpr的核苷酸序列预防淋巴细胞活化的方法。 治疗患有或怀疑患有自身免疫疾病的个体的方法,通过施用vpr蛋白或其功能片段或包含编码vpr蛋白的核苷酸序列的核酸分子的核酸分子,或者包含编码vpr蛋白的核苷酸序列的核酸分子, 公开了其功能片段。 公开了将活性剂递送至细胞核的共轭组合物。

    Compositions and methods for delivery of genetic material
    8.
    发明授权
    Compositions and methods for delivery of genetic material 失效
    用于遗传物质传递的组合物和方法

    公开(公告)号:US5981505A

    公开(公告)日:1999-11-09

    申请号:US979385

    申请日:1997-11-26

    摘要: Methods of inducing genetic material into cells of an individual and compositions and kits for practicing the same are disclosed. The methods comprise the steps of contacting cells of an individual with a polynucleotide function enhancer and administering to the cells, a nucleic acid molecule that is free of retroviral particles. The nucleic acid molecule comprises a nucleotide sequence that encodes a protein that comprises at least one epitope that is identical or substantially similar to an epitope of a pathogen antigen or an antigen associated with a hyperproliferative or autoimmune disease, a protein otherwise missing from the individual due to a missing, non-functional or partially functioning gene, or a protein that produces a therapeutic effect on an individual. Methods of prophylactically and therapeutically immunizing an individual against HIV are disclosed. Pharmaceutical compositions and kits for practicing methods of the present invention are disclosed.

    摘要翻译: PCT No.PCT / US94 / 00899 Sec。 371日期:1995年8月28日 102(e)日期1995年8月28日PCT 1994年1月26日PCT PCT。 公开号WO94 / 16737 日期1994年8月4日公开了将遗传物质诱导入个体细胞的方法和用于实施其的组合物和试剂盒。 所述方法包括使个体的细胞与多核苷酸功能增强子接触并向细胞施用不含逆转录病毒颗粒的核酸分子的步骤。 核酸分子包含编码蛋白质的核苷酸序列,该蛋白质包含与病原体抗原或与过度增殖或自身免疫疾病相关的抗原的表位相同或基本相似的至少一个表位, 涉及缺失的,非功能的或部分功能的基因或对个体产生治疗作用的蛋白质。 公开了预防和治疗个体免受HIV感染的方法。 公开了用于本发明的实践方法的药物组合物和试剂盒。

    Compositions and methods for delivery of genetic material
    10.
    发明授权
    Compositions and methods for delivery of genetic material 有权
    用于遗传物质传递的组合物和方法

    公开(公告)号:US07001759B1

    公开(公告)日:2006-02-21

    申请号:US09359975

    申请日:1999-07-23

    摘要: Methods of introducing genetic material into cells of an individual and compositions and kits for practicing the same are disclosed. The methods comprise the steps of contacting cells of an individual with a polynucleotide function enhancer and administering to the cells, a nucleic acid molecule that is free of retroviral particles. The nucleic acid molecule comprises a nucleotide sequence that encodes a protein that comprises at least one epitope that is identical or substantially similar to an epitope of a pathogen antigen or an antigen associated with a hyperproliferative or autoimmune disease, a protein otherwise missing from the individual due to a missing, non-functional, or partially functioning gene, or a protein that produces a therapeutic effect on an individual. Methods of prophylactically and therapeutically immunizing an individual against pathogens are disclosed. Pharmaceutical compositions and kits for practicing methods of the present invention are disclosed.

    摘要翻译: 公开了将遗传物质引入个体细胞的方法和用于实施其的组合物和试剂盒。 所述方法包括使个体的细胞与多核苷酸功能增强子接触并向细胞施用不含逆转录病毒颗粒的核酸分子的步骤。 核酸分子包含编码蛋白质的核苷酸序列,该蛋白质包含与病原体抗原或与过度增殖或自身免疫疾病相关的抗原的表位相同或基本相似的至少一个表位, 涉及一种缺失的,非功能的或部分功能的基因或对个体产生治疗作用的蛋白质。 公开了预防和治疗个体免受病原体的方法。 公开了用于本发明的实践方法的药物组合物和试剂盒。