Purposeful movement of human migratory cells away from an agent source
    1.
    发明授权
    Purposeful movement of human migratory cells away from an agent source 有权
    人类迁徙细胞有目的地移动远离代理来源

    公开(公告)号:US07775469B2

    公开(公告)日:2010-08-17

    申请号:US11407477

    申请日:2006-04-20

    IPC分类号: A61K39/00 A61K45/00

    摘要: This invention relates to methods and compositions for modulating movement of eukaryotic cells with migratory capacity. More specifically, the invention relates to methods and compositions for modulating movement of cells of hematopoietic, neural, epithelial, or mesenchymal origin, in a specific site in a subject. The foregoing are useful, inter alia, in the treatment of conditions characterized by a need to modulate migratory-cell movement associated with specific sites in a subject. More specifically, specific sites include sites of inflammation and modulation of migratory-cell movement is movement away from an agent source, or repulsion. Other sites include tumor sites, sites of pathogenic infection, and germ cell bearing sites.

    摘要翻译: 本发明涉及用迁移能力调节真核细胞运动的方法和组合物。 更具体地,本发明涉及用于调节受试者的特定部位中造血,神经,上皮或间质来源的细胞运动的方法和组合物。 前述内容尤其可用于治疗特征在于需要调节与受试者中特定部位相关的迁移细胞运动的病症。 更具体地,特定部位包括炎症部位和迁移细胞运动的调节是远离药剂来源的运动或排斥。 其他部位包括肿瘤部位,病原体感染部位和生殖细胞承载部位。

    Nucleic acid encoding eotaxin
    3.
    发明授权
    Nucleic acid encoding eotaxin 失效
    编码嗜酸性粒细胞趋化因子的核酸

    公开(公告)号:US06403782B1

    公开(公告)日:2002-06-11

    申请号:US09366887

    申请日:1999-08-04

    IPC分类号: C12N1519

    CPC分类号: C07K14/523 A61K38/00

    摘要: Disclosed is substantially pure eotaxin DNA sequence and eotaxin polypeptide, and methods of using such DNA and polypeptide to direct chemotaxis of eosinophils. Methods are provided for the treatment diseases and disorders such as inflammation and tumorigenesis.

    摘要翻译: 公开了基本上纯的嗜酸性粒细胞趋化嗜热性嗜酸细胞活化趋化因子DNA序列和嗜酸细胞活化趋化因子多肽,以及使用这种DNA和多肽来指导嗜酸性粒细胞趋化性的方法。 提供了治疗诸如炎症和肿瘤发生的疾病和病症的方法。

    Nucleic acid encoding monocyte chemotactic protein 4
    4.
    发明授权
    Nucleic acid encoding monocyte chemotactic protein 4 失效
    核酸编码单核细胞趋化蛋白4

    公开(公告)号:US06673915B1

    公开(公告)日:2004-01-06

    申请号:US09545894

    申请日:2000-04-07

    IPC分类号: C12N1519

    摘要: Substantially pure nucleic acid molecules encoding the monocyte chemotactic proteins MCP-4 and MCP-5. These molecules and the polypeptides they encode are useful in treating diseases or conditions that: (1) are exacerbated by a local immune response, (2) would benefit from a local immune response, or (3) are caused by infectious agents that gain entry to mammalian cells via the chemokine receptors bound by MCP-4 or MCP-5.

    摘要翻译: 编码单核细胞趋化蛋白MCP-4和MCP-5的基本纯的核酸分子。 这些分子及其编码的多肽可用于治疗以下疾病或病症:(1)由局部免疫应答加剧,(2)将受益于局部免疫应答,或(3)由获得进入的感染因子引起 通过MCP-4或MCP-5结合的趋化因子受体与哺乳动物细胞接触。

    Eotaxin: an eosinophil chemoattractant
    5.
    发明授权
    Eotaxin: an eosinophil chemoattractant 失效
    嗜酸性粒细胞趋化因子:嗜酸性粒细胞趋化因子

    公开(公告)号:US06780973B1

    公开(公告)日:2004-08-24

    申请号:US09517204

    申请日:2000-03-02

    IPC分类号: C07K1452

    CPC分类号: C07K14/523 A61K38/00

    摘要: Disclosed is substantially pure eotaxin DNA sequence and eotaxin polypeptide, and methods of using such DNA and polypeptide to direct chemotaxis of eosinophils. Methods are provided for the treatment diseases and disorders such as inflammation and tumorigenesis.

    摘要翻译: 公开了基本上纯的嗜酸性粒细胞趋化嗜热性嗜酸细胞活化趋化因子DNA序列和嗜酸细胞活化趋化因子多肽,以及使用这种DNA和多肽来指导嗜酸性粒细胞趋化性的方法。 提供了治疗诸如炎症和肿瘤发生的疾病和病症的方法。

    LYSOPHOSPHATIDIC ACID RECEPTOR TARGETING FOR LUNG DISEASE
    8.
    发明申请
    LYSOPHOSPHATIDIC ACID RECEPTOR TARGETING FOR LUNG DISEASE 审中-公开
    LOSOPHOSPHATIDIC酸受体靶向肺病

    公开(公告)号:US20100143381A1

    公开(公告)日:2010-06-10

    申请号:US12450051

    申请日:2008-03-11

    CPC分类号: C07K14/705

    摘要: The present invention contemplates that lysophosphatidic acid (LPA) may be induced by lung injury and may be responsible for aberrant wound-healing responses. For example, in a bleomycin model of pulmonary fibrosis LPAi deficient mice are protected from pulmonary fibrosis and mortality. Specifically, chemotactic-induced fibroblast responses, lung fibroblast accumulation, and vascular permeability increases were all attenuated. In contrast, however, bleomycin-induced leukocyte recruitment was preserved. These results demonstrate that LPAi activity may link pulmonary fibrosis with lung injury by mediating fibroblast recruitment and vascular leak. The present invention therefore represents LPAi as a new target to treat lung diseases including, but not limited to, fibrosis, idiopathic pulmonary fibrosis, and acute respiratory distress syndrome.

    摘要翻译: 本发明考虑到溶血磷脂酸(LPA)可能由肺损伤引起,并且可能导致异常的伤口愈合反应。 例如,在肺纤维化的博来霉素模型中,LPAi缺陷小鼠被保护免于肺纤维化和死亡。 具体来说,趋化性诱导的成纤维细胞反应,肺成纤维细胞的积累和血管通透性的增加都被减弱。 然而,相比之下,博来霉素诱导的白细胞募集被保留。 这些结果表明LPAi活性可能通过介导成纤维细胞募集和血管渗漏而将肺纤维化与肺损伤联系起来。 因此,本发明代表LPAi作为治疗肺部疾病的新靶标,包括但不限于纤维化,特发性肺纤维化和急性呼吸窘迫综合征。