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    • 46. 发明申请
    • Hepatitis C virus gene products
    • 丙型肝炎病毒基因产物
    • US20020076415A1
    • 2002-06-20
    • US09736959
    • 2000-12-14
    • Jing-Hsiung OuZhenming Xu
    • A61K039/29C12Q001/70C07H021/04C07K014/01C07K016/08
    • C07K14/005A61K39/00A61K2039/53C07K16/109C12N2770/24222
    • The present invention provides heretofore unidentified proteins and smaller peptides of HCV, which are produced by translation of the HCV core RNA through a frameshifting mechanism. In one embodiment the invention provides a protein that is about 125 to about 161 amino acids long depending on the HCV genotypes. The smaller peptides of the invention range in length from about 13 amino acids to over 50 amino acids. The invention also includes DNA sequences that encode the polypeptides of the invention, antibodies directed against the polypeptides of the invention, and therapeutic compositions including vaccines and anti-viral compositions. Additionally, the invention provides for methods for diagnosing, preventing and treating hepatitis C using the compounds and compositions of the invention.
    • 本发明提供了迄今为止未知的蛋白质和较小的HCV肽,其通过通过移码机制翻译HCV核心RNA产生。 在一个实施方案中,本发明提供了约125至约161个氨基酸长度的蛋白质,这取决于HCV基因型。 本发明较小的肽的长度范围为约13个氨基酸至超过50个氨基酸。 本发明还包括编码本发明多肽的DNA序列,针对本发明多肽的抗体,以及包括疫苗和抗病毒组合物的治疗组合物。 此外,本发明提供了使用本发明的化合物和组合物诊断,预防和治疗丙型肝炎的方法。
    • 50. 发明申请
    • Superantigen enhancement of specific immune responses
    • 超抗原增强特异性免疫反应
    • US20010046501A1
    • 2001-11-29
    • US09808718
    • 2001-03-15
    • Howard M. JohnsonBarbara A. TorresKominsky L. Scott
    • A61K039/21A61K039/29A61K039/00
    • A61K39/0011A61K2039/5152A61K2039/55544A61K2039/57
    • The invention relates to superantigen mediated expansion of antigen-specific T cells for cancer and infectious agent treatment/prophylaxis. Mice were injected with inactivated B16F10 mouse melanoma cells, followed by injection with a combined SEA/SEB injection or a sham injection on days 3 and 6, followed by day 4 challenge with live melanoma cells. The SEA/SEB recipient mice survived longer post-challenge and had a higher CTLs against tumor cells than did the sham injected mice. SEA/SEB TCR activation has been reported to be independent of antigen specificity of TCRs. This invention provides a method whereby a combination of Staphylococcal enterotoxin superantigens is used to enhance specific immune responses to activating antigens to enhance immune responses against cancers and infectious agents.
    • 本发明涉及抗原特异性T细胞用于癌症和感染剂治疗/预防的超抗原介导的扩增。 向小鼠注射灭活的B16F10小鼠黑素瘤细胞,随后在第3天和第6天用SEA / SEB联合注射或假注射注射,随后用活黑素瘤细胞进行第4天的攻击。 SEA / SEB受体小鼠在攻击后存活时间更长,与假注射的小鼠相比,肿瘤细胞的CTLs更高。 据报道SEA / SEB TCR活化与TCR的抗原特异性无关。 本发明提供了一种方法,其中葡萄球菌肠毒素超抗原的组合用于增强对活化抗原的特异性免疫应答,以增强针对癌症和感染因子的免疫应答。