TYPE 1 INTEFERON DIAGNOSTIC
    1.
    发明申请
    TYPE 1 INTEFERON DIAGNOSTIC 审中-公开
    类型1 INTEFERON诊断

    公开(公告)号:US20120251546A1

    公开(公告)日:2012-10-04

    申请号:US13393616

    申请日:2010-09-02

    摘要: The present disclosure encompasses type-I IFN and IFNα-induced PD marker expression profiles, kits, and methods for identifying such IFNα-induced PD marker expression profiles. The type-I IFN and IFNα-induced PD marker expression profiles may also be used in, for example, methods of treating patients having a type-I IFN or IFNα-mediated disorder, methods of monitoring disease progression of patients receiving treatment with a therapeutic agent that modulates type 1 interferon activity, identifying patients as candidates to receive a therapeutic that binds to and neutralizes IFNα activity, and in diagnosing or providing a prognosis to patients having IFNα-induced disorders.

    摘要翻译: 本公开内容涵盖I型IFN和IFNα诱导的PD标志物表达谱,试剂盒和用于鉴定这种IFNα诱导的PD标志物表达谱的方法。 I型IFN和IFNα诱导的PD标志物表达谱也可用于例如治疗患有I型IFN或IFNα介导的病症的患者的方法,监测接受治疗的患者的疾病进展的方法 调节1型干扰素活性的试剂,鉴定患者作为接受结合并中和IFNα活性的治疗剂的候选物,以及诊断或提供具有IFNα诱导的病症的患者的预后。

    Therapeutic targeting of PARC/CCL18 and its signaling in pulmonary fibrosis
    4.
    发明申请
    Therapeutic targeting of PARC/CCL18 and its signaling in pulmonary fibrosis 审中-公开
    PARC / CCL18的治疗靶向及其在肺纤维化中的信号传导

    公开(公告)号:US20060009452A1

    公开(公告)日:2006-01-12

    申请号:US11143707

    申请日:2005-06-03

    IPC分类号: A61K31/5377

    摘要: The present invention relates to methods of treating, preventing or preventing the progression of fibrosis comprising inhibiting the actions of pulmonary and activation-regulated chemokine (PARC) or at least one of its downstream effector molecules, such as Sp1 transcription factor and protein kinase C-alpha (PKCα). The present invention also relates to methods of screening and/or identifying compounds useful for the treatment of fibrosis comprising contacting PARC or its downstream effector molecules, such as Sp1 or PKCα, with a substance and subsequently determining the effects of the substance on the activity of PARC or Sp1 or PKCα. The present invention also relates to methods of screening and/or identifying compounds that prevent or inhibit collagen deposition comprising contacting PARC or its downstream effector molecules, such as Sp1 or PKCα, with a substance and subsequently determining the effects of the substance on the activity of PARC or Sp1 or PKCα.

    摘要翻译: 本发明涉及治疗,预防或预防纤维化进展的方法,包括抑制肺和活化调节的趋化因子(PARC)或其至少一种下游效应分子如Sp1转录因子和蛋白激酶C- α(PKCalpha)。 本发明还涉及筛选和/或鉴定可用于治疗纤维化的化合物的方法,包括将PARC或其下游效应分子如Sp1或PKCα与物质接触,随后确定物质对活性的影响 PARC或Sp1或PKCalpha。 本发明还涉及筛选和/或鉴定预防或抑制胶原蛋白沉积的化合物的方法,其包括将PARC或其下游效应分子如Sp1或PKCα与物质接触,随后确定物质对活性的影响 PARC或Sp1或PKCalpha。

    INTERFERON ALPHA-INDUCED PHARMACODYNAMIC MARKERS
    5.
    发明申请
    INTERFERON ALPHA-INDUCED PHARMACODYNAMIC MARKERS 审中-公开
    干扰素诱导的药物动力学标记

    公开(公告)号:US20110287022A1

    公开(公告)日:2011-11-24

    申请号:US12999626

    申请日:2009-06-19

    摘要: The present invention encompasses type-I IFN and IFNα-induced PD marker expression profiles, kits, and methods for identifying such IFNα-induced PD marker expression profiles. The type-I IFN and IFNα-induced PD marker expression profiles may also be used in, for example, methods of treating patients having a type-I IFN or IFNα-mediated disorder, methods of monitoring disease progression of patients receiving treatment with a therapeutic agent that binds to and modulates IFNα activity, identifying patients as candidates to receive a therapeutic that binds to and neutralizes IFNα activity, and in diagnosing or providing a prognoses to patients having IFNα-induced disorders.

    摘要翻译: 本发明包括I型IFN和IFNα诱导的PD标志物表达谱,试剂盒和用于鉴定这种IFNα诱导的PD标志物表达谱的方法。 I型IFN和IFNα诱导的PD标志物表达谱也可用于例如治疗患有I型IFN或IFNα介导的病症的患者的方法,监测接受治疗的患者的疾病进展的方法 结合并调节IFNα活性的试剂,鉴定患者作为接受结合并中和IFNα活性的治疗剂的候选物,以及诊断或提供具有IFNα诱导的病症的患者的预后。

    Methods of reducing eosinophil levels
    6.
    发明授权
    Methods of reducing eosinophil levels 有权
    减少嗜酸性粒细胞水平的方法

    公开(公告)号:US08501176B2

    公开(公告)日:2013-08-06

    申请号:US13177221

    申请日:2011-07-06

    IPC分类号: A61K39/395 C07K16/28

    摘要: The present invention relates to a method of reducing the numbers of eosinophils in a human subject comprising administration to a subject an IL-5R binding molecule that comprises (a) a region that specifically binds to the IL-5R and (b) an immunoglobulin Fc region. In a specific embodiment, a method of the invention reduces the number of eosinophils in blood, bone marrow, gastrointestinal tract (e.g. esophagus, stomach, small intestine and colon), or lung.

    摘要翻译: 本发明涉及一种减少人受试者嗜酸性粒细胞数量的方法,包括向受试者施用包含(a)特异性结合IL-5R的区域和(b)免疫球蛋白Fc的IL-5R结合分子 地区。 在具体实施方案中,本发明的方法减少血液,骨髓,胃肠道(例如食道,胃,小肠和结肠)或肺中嗜酸性粒细胞的数量。

    METHODS OF REDUCING EOSINOPHIL LEVELS
    7.
    发明申请
    METHODS OF REDUCING EOSINOPHIL LEVELS 审中-公开
    降低雌激素水平的方法

    公开(公告)号:US20100291073A1

    公开(公告)日:2010-11-18

    申请号:US12600017

    申请日:2008-05-14

    摘要: The present invention relates to a method of reducing the numbers of eosinophils in a human subject comprising administration to a subject an IL-5R binding molecule that comprises (a) a region that specifically binds to the IL-5R and (b) an immunoglobulin Fc region. In a specific embodiment, a method of the invention reduces the number of eosinophils in blood, bone marrow, gastrointestinal tract (e g, esophagus, stomach, small intestine and colon), or lung.

    摘要翻译: 本发明涉及一种减少人受试者嗜酸性粒细胞数量的方法,包括向受试者施用包含(a)特异性结合IL-5R的区域和(b)免疫球蛋白Fc的IL-5R结合分子 地区。 在具体实施方案中,本发明的方法减少血液,骨髓,胃肠道(例如食道,胃,小肠和结肠)或肺中嗜酸性粒细胞的数量。