VACUNA BIOLOGICA AUTOLOGA CONTRA EL CANCER
    62.
    发明申请
    VACUNA BIOLOGICA AUTOLOGA CONTRA EL CANCER 审中-公开
    自动生物癌症疫苗

    公开(公告)号:WO2011135393A1

    公开(公告)日:2011-11-03

    申请号:PCT/IB2010/000977

    申请日:2010-04-27

    IPC分类号: A61K39/00 A61P35/00 A61K39/23

    摘要: La presente invención se relaciona con una vacuna biológica autóloga contra el cáncer y su método de preparación. La vacuna de Ia presente solicitud es una vacuna biológica obtenida a partir de las proteínas sobreexpresadas en el suero de los pacientes con cáncer, a las que se ha agregado adyuvantes inmunológicos tales como un virus ADN atenuado y aminoácidos con el fin de provocar una respuesta inmune, bloqueando las células tumorales. Su método de preparación comprende Ia obtención del antígeno asociado al tumor así como del preparado vacunal con virus ADN atenuado, Ia mezcla de los componentes bajo condiciones que han sido determinadas por experimentación, filtración y refrigeración.

    摘要翻译: 本发明涉及自体生物癌疫苗及其制备方法。 本申请的疫苗是从癌症患者的血清中的过表达蛋白获得的生物疫苗,已经加入免疫佐剂如减毒病毒DNA和氨基酸的蛋白质,以引起免疫应答,阻断肿瘤细胞。 制备方法包括获得与肿瘤相关的抗原以及具有减毒病毒DNA的疫苗制剂,在通过实验,过滤和制冷测定的条件下将组分组合。

    HYDROGELS FOR COMBINATORIAL DELIVERY OF IMMUNE-MODULATING BIOMOLECULES
    68.
    发明申请
    HYDROGELS FOR COMBINATORIAL DELIVERY OF IMMUNE-MODULATING BIOMOLECULES 审中-公开
    用于组合输送免疫调节生物分子的HYDROGEL

    公开(公告)号:WO2010123971A3

    公开(公告)日:2011-03-03

    申请号:PCT/US2010031866

    申请日:2010-04-21

    摘要: One embodiment of the current disclosure relates to an immune-modulating composition comprising a hydrogel-forming polymer, an immune-modulating biomolecule operable to recruit or retain an immune cell, and an antigen-related biomolecule. Another embodiment of the current disclosure relates to a method of providing an antigen to an antigen presenting cell in an animal by administering to the animal at an administration site an immune-modulating composition as described above. Next, one forms a hydrogel in-situ from the hydrogel-forming polymer, then recruits at least one antigen presenting cell to the administration site using the immune-modulating biomolecule, and finally inducing phagocytosis of the at least one antigen- related biomolecule by the antigen presenting cell.

    摘要翻译: 本公开的一个实施方案涉及包含水凝胶形成聚合物,可操作以募集或保留免疫细胞的免疫调节生物分子和抗原相关生物分子的免疫调节组合物。 本公开的另一个实施方案涉及通过在给药部位向动物施用如上所述的免疫调节组合物来向动物中的抗原呈递细胞提供抗原的方法。 接下来,从形成水凝胶的聚合物原位形成水凝胶,然后使用免疫调节生物分子将至少一种抗原呈递细胞募集到给药部位,最后通过所述免疫调节生物分子诱导至少一种与抗原相关的生物分子的吞噬作用 抗原呈递细胞。

    MODULATION OF SGK1 EXPRESSION IN TH17 CELLS TO MODULATE TH17-MEDIATED IMMUNE RESPONSES
    69.
    发明申请
    MODULATION OF SGK1 EXPRESSION IN TH17 CELLS TO MODULATE TH17-MEDIATED IMMUNE RESPONSES 审中-公开
    TH17细胞中SGK1表达的调节以调节TH17介导的免疫应答

    公开(公告)号:WO2011014775A1

    公开(公告)日:2011-02-03

    申请号:PCT/US2010/043907

    申请日:2010-07-30

    摘要: The inventors have made the surprising discovery that SGK1, a serine/threonine kinase previously described as being involved in regulation of cellular sodium homeostasis, has a novel and unexpected function in the differentiation and function of a specific subset of CD4 T cells, the TH17 lineage. Described herein are methods and compositions for modulation of TH17 cell differentiation, proliferation, and/or function that rely upon modulating the activity or expression of SGK1. Such methods and compositions are useful in the treatment of disorders including autoimmune diseases, chronic inflammatory conditions, infectious diseases, and cancer.

    摘要翻译: 本发明人已经令人惊奇地发现,SGK1(丝氨酸/苏氨酸激酶以前被描述为参与细胞钠稳态调节)在CD4T细胞的特定子集的分化和功能中具有新颖和意想不到的功能,TH17谱系 。 本文描述了用于调节依赖于调节SGK1的活性或表达的TH17细胞分化,增殖和/或功能的方法和组合物。 这些方法和组合物可用于治疗包括自身免疫性疾病,慢性炎性病症,感染性疾病和癌症的病症。

    SCHISTOSOMIASIS VACCINE COMPOSITIONS AND METHODS OF USE
    70.
    发明申请
    SCHISTOSOMIASIS VACCINE COMPOSITIONS AND METHODS OF USE 审中-公开
    血吸虫病疫苗组合物和使用方法

    公开(公告)号:WO2011005593A2

    公开(公告)日:2011-01-13

    申请号:PCT/US2010039707

    申请日:2010-06-23

    摘要: No effective vaccine exists for the devastating parasitic disease of Schistosomiasis. The present invention focuses on Sm-p80, a functionally important antigen of Schistosoma mansoni that plays a pivotal role in the schistosome immune evasion process. When used in a novel vaccine formulation, Sm-p80 demonstrates consistent immunogenicity, protective potential, and antifecundity effects. Two novel DNA constructs were made for immunization purposes. Sm- p80 coding sequence was cloned into VR 1020. Additionally, Sm-p80 coding sequence was cloned into pcDNA3.1 with flanking CpG motifs on each end of the Sm-p80 sequence. When used in different vaccine formulations, both of the constructs demonstrate the superior antifecundity and anti-worm effects of Sm-p80, which has great potential as an important vaccine candidate for the reduction of the morbidity associated with schistosome infection.

    摘要翻译: 对于血吸虫病的破坏性寄生虫病没有有效的疫苗。 本发明集中于在血吸虫免疫逃避过程中起关键作用的曼氏血吸虫的功能重要抗原Sm-p80。 当用于新型疫苗制剂时,Sm-p80表现出一致的免疫原性,保护潜力和抗真菌作用。 为了免疫目的制造了两种新型DNA构建体。 将Sm-p80编码序列克隆到VR1020中。另外,将Sm-p80编码序列克隆到在Sm-p80序列的每一端具有侧翼CpG基序的pcDNA3.1中。 当用于不同的疫苗制剂时,两种构建体均表现出Sm-p80的优异的抗真菌和抗蠕虫效果,其作为降低与血吸虫感染相关的发病率的重要候选疫苗具有巨大潜力。