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    • 2. 发明申请
    • IL-16 ANTAGONISTS
    • IL-16拮抗剂
    • WO0110891A3
    • 2001-08-16
    • PCT/US0021228
    • 2000-08-04
    • RES CORP TECHNOLOGIES INC
    • CRUICKSHANK WILLIAM WKORNFELD HARRYCENTER DAVID M
    • A61K38/00A61K38/08C07K5/103C07K7/06C07K14/73C07K14/705A61K38/17A61P29/00C07K16/28C12N15/13
    • C07K7/06A61K38/00C07K5/1013C07K14/70514
    • In accordance with the present invention, novel IL-16 antagonists, preferably peptides derived from CD4, have been isolated and synthesized. These peptides possess IL-16 antagonistic properties including the ability to selectively bind to IL-16 and inhibit IL-16-mediated biological activity. The peptides comprise specific portions of the native human CD4 receptor and variations thereof and therefore are non-immunogenic when administered to humans. The present invention also provides compositions containing at least one IL-16 antagonist peptide which can inhibit, suppress or cause the cessation of at least one IL-16-mediated biological activity in mammals, including humans. The present invention provides a method and composition for treating inflammation associated with disease states such as asthma, rheumatoid arthritis, inflammatory bowel disease (IBD) and systemic lupus (SLE) in mammals such as, for example, humans.
    • 根据本发明,已经分离并合成了新的IL-16拮抗剂,优选来源于CD4的肽。 这些肽具有IL-16拮抗特性,包括选择性结合IL-16和抑制IL-16介导的生物学活性的能力。 肽包含天然人CD4受体的特定部分及其变体,因此当给予人时是非免疫原性的。 本发明还提供了包含至少一种IL-16拮抗剂肽的组合物,其可抑制,抑制或引起哺乳动物(包括人)中至少一种IL-16介导的生物学活性的停止。 本发明提供了用于在哺乳动物例如人中治疗与疾病状态相关的炎症例如哮喘,类风湿性关节炎,炎性肠病(IBD)和系统性红斑狼疮(SLE)的方法和组合物。