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    • 4. 发明授权
    • Prevention of primary and metastatic neoplastic diseases with hsp70-peptide complexes
    • 用hsp70肽复合物预防原发性和转移性肿瘤疾病
    • US06455048B1
    • 2002-09-24
    • US09440173
    • 1999-11-15
    • Pramod K. SrivastavaRajiv Y. Chandawarkar
    • Pramod K. SrivastavaRajiv Y. Chandawarkar
    • A61K39385
    • A61K39/0011A61K2039/6043A61K2039/622Y02A50/466
    • The present invention relates to methods and compositions for eliciting an immune response and the prevention and treatment of primary and metastatic neoplastic diseases and infectious diseases. The methods of the invention comprise administering a composition comprising an effective amount of a complex, in which the complex consists essentially of a heat shock protein (hsp) noncovalently bound to an antigenic molecule. Optionally, the methods further comprise administering antigen presenting cells sensitized with complexes of hsps noncovalently bound to an antigenic molecule. “Antigenic molecule” as used herein refers to the peptides with which the hsps are endogenously associated in vivo as well as exogenous antigens/immunogens (i.e., with which the hsps are not complexed in vivo) or antigenic/immunogenic fragments and derivatives thereof. In a preferred embodiment, the complex is autologous to the individual. In a specific embodiment, the effective amounts of the complex are in the range of 0.1 to 9.0 micrograms for complexes comprising hsp70, 5 to 49 micrograms for hsp90, and 0.1 to 9.0 micrograms for gp96.
    • 本发明涉及引发免疫应答和预防和治疗原发性和转移性肿瘤性疾病和传染病的方法和组合物。 本发明的方法包括施用包含有效量的复合物的组合物,其中复合物基本上由非共价结合于抗原分子的热休克蛋白(hsp)组成。 任选地,所述方法还包括施用用非共价结合于抗原分子的hsps复合物致敏的抗原呈递细胞。 本文所用的“抗原分子”是指hsps与体内内源性相关的肽以及外源性抗原/免疫原(即hsps在体内不复合)或其抗原/免疫原性片段及其衍生物。 在优选的实施方案中,复合物是个体自体的。 在一个具体实施方案中,对于包含hsp70,5-449微克对于hsp90和对于gp96为0.1至9.0微克的复合物,复合物的有效量在0.1至9.0微克范围内。
    • 5. 发明授权
    • Prevention of infectious diseases with hsp70-peptide complexes
    • 用hsp70肽复合物预防传染病
    • US06399069B1
    • 2002-06-04
    • US09439684
    • 1999-11-15
    • Pramod K. SrivastavaRajiv Y. Chandawarkar
    • Pramod K. SrivastavaRajiv Y. Chandawarkar
    • A61K39385
    • A61K39/0011A61K2039/6043A61K2039/622Y02A50/466
    • The present invention relates to methods and compositions for eliciting an immune response and the prevention and treatment of primary and metastatic neoplastic diseases and infectious diseases. The methods of the invention comprise administering a composition comprising an effective amount of a complex, in which the complex consists essentially of a heat shock protein (hsp) noncovalently bound to an antigenic molecule. Optionally, the methods further comprise administering antigen presenting cells sensitized with complexes of hsps noncovalently bound to an antigenic molecule. “Antigenic molecule” as used herein refers to the peptides with which the hsps are endogenously associated in vivo as well as exogenous antigens/immunogens (i.e., with which the hsps are not complexed in vivo) or antigenic/immunogenic fragments and derivatives thereof. In a preferred embodiment, the complex is autologous to the individual. In a specific embodiment, the effective amounts of the complex are in the range of 0.1 to 9.0 micrograms for complexes comprising hsp70, 5 to 49 micrograms for hsp90, and 0.1 to 9.0 micrograms for gp96.
    • 本发明涉及引发免疫应答和预防和治疗原发性和转移性肿瘤性疾病和传染病的方法和组合物。 本发明的方法包括施用包含有效量的复合物的组合物,其中复合物基本上由非共价结合于抗原分子的热休克蛋白(hsp)组成。 任选地,所述方法还包括施用用非共价结合于抗原分子的hsps复合物致敏的抗原呈递细胞。 本文所用的“抗原分子”是指hsps与体内内源性相关的肽以及外源性抗原/免疫原(即hsps在体内不复合)或其抗原/免疫原性片段及其衍生物。 在优选的实施方案中,复合物是个体自体的。 在一个具体实施方案中,对于包含hsp70,5-449微克对于hsp90和对于gp96为0.1至9.0微克的复合物,复合物的有效量在0.1至9.0微克范围内。
    • 6. 发明授权
    • Methods and compositions for eliciting an immune response with hsp70-peptide complexes
    • 用hsp70-肽复合物引发免疫应答的方法和组合物
    • US06383493B1
    • 2002-05-07
    • US09440171
    • 1999-11-15
    • Pramod K. SrivastavaRajiv Y. Chandawarkar
    • Pramod K. SrivastavaRajiv Y. Chandawarkar
    • A61K39385
    • A61K39/0011A61K2039/6043A61K2039/622Y02A50/466
    • The present invention relates to methods and compositions for eliciting an immune response and the prevention-and treatment of primary and metastatic neoplastic diseases and infectious diseases. The methods of the invention comprise administering a composition comprising an effective amount of a complex, in which the complex consists essentially of a heat shock protein (hsp) noncovalently bound to an antigenic molecule. Optionally, the methods further comprise administering antigen presenting cells sensitized with complexes-of hsps noncovalently bound to an antigenic molecule. “Antigenic molecule” as used herein refers to the peptides with which the hsps are endogenously associated in vivo as well as exogenous antigens/immunogens (i.e., with which the hsps are not complexed in vivo) or antigenic/immunogenic fragments and derivatives thereof. In a preferred embodiment, the complex is autologous to the individual. In a specific embodiment, the effective amounts of the complex are in the range of 0.1 to 9.0 micrograms for complexes comprising hsp70, 5 to 49 micrograms for hsp90, and 0.1 to 9.0 micrograms for gp96.
    • 本发明涉及引发免疫应答的方法和组合物以及预防和治疗原发性和转移性肿瘤性疾病和感染性疾病。 本发明的方法包括施用包含有效量的复合物的组合物,其中复合物基本上由非共价结合于抗原分子的热休克蛋白(hsp)组成。 任选地,所述方法还包括施用用非共价结合到抗原分子的hsps复合物敏化的抗原呈递细胞。 本文所用的“抗原分子”是指hsps与体内内源性相关的肽以及外源性抗原/免疫原(即hsps在体内不复合)或其抗原/免疫原性片段及其衍生物。 在优选的实施方案中,复合物是个体自体的。 在一个具体实施方案中,对于包含hsp70,5-449微克对于hsp90和对于gp96为0.1至9.0微克的复合物,复合物的有效量在0.1至9.0微克范围内。
    • 7. 发明授权
    • Prevention of infectious diseases with gp96-peptide complexes
    • 用gp96肽复合物预防传染病
    • US06379672B1
    • 2002-04-30
    • US09439683
    • 1999-11-15
    • Pramod K. SrivastavaRajiv Y. Chandawarkar
    • Pramod K. SrivastavaRajiv Y. Chandawarkar
    • A61K39385
    • A61K39/0011A61K2039/6043A61K2039/622Y02A50/466
    • The present invention relates to methods and compositions for eliciting an immune response and the prevention and treatment of primary and metastatic neoplastic diseases and infectious diseases. The methods of the invention comprise administering a composition comprising an effective amount of a complex, in which the complex consists essentially of a heat shock protein (hsp) noncovalently bound to an antigenic molecule. Optionally, the methods further comprise administering antigen presenting cells sensitized with complexes of hsps noncovalently bound to an antigenic molecule. “Antigenic molecule” as used herein refers to the peptides with which the hsps are endogenously associated in vivo as well as exogenous antigens/immunogens (i.e., with which the hsps are not complexed in vivo) or antigenic/immunogenic fragments and derivatives thereof. In a preferred embodiment, the complex is autologous to the individual. In a specific embodiment, the effective amounts of the complex are in the range of 0.1 to 9.0 micrograms for complexes comprising hsp70, 5 to 49 micrograms for hsp90, and 0.1 to 9.0 micrograms for gp96.
    • 本发明涉及引发免疫应答和预防和治疗原发性和转移性肿瘤性疾病和传染病的方法和组合物。 本发明的方法包括施用包含有效量的复合物的组合物,其中复合物基本上由非共价结合于抗原分子的热休克蛋白(hsp)组成。 任选地,所述方法还包括施用用非共价结合于抗原分子的hsps复合物致敏的抗原呈递细胞。 本文所用的“抗原分子”是指hsps与体内内源性相关的肽以及外源性抗原/免疫原(即hsps在体内不复合)或其抗原性/免疫原性片段及其衍生物。 在优选的实施方案中,复合物是个体自体的。 在一个具体实施方案中,对于包含hsp70,5-449微克对于hsp90和对于gp96为0.1至9.0微克的复合物,复合物的有效量在0.1至9.0微克范围内。