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    • 1. 发明授权
    • IL-16 antagonists
    • IL-16拮抗剂
    • US07232801B2
    • 2007-06-19
    • US11167710
    • 2005-06-27
    • David M. CenterWilliam W. CruikshankHardy Kornfeld
    • David M. CenterWilliam W. CruikshankHardy Kornfeld
    • A61K38/08A61K38/04A61K38/00A61K45/00C07K7/06
    • 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,优选衍生自CD4的肽。 这些肽具有IL-16拮抗性质,包括选择性结合IL-16并抑制IL-16介导的生物活性的能力。 肽包含天然人CD4受体的特定部分及其变体,因此在给予人时是非免疫原性的。 本发明还提供含有至少一种IL-16拮抗剂肽的组合物,其可以抑制,抑制或引起包括人在内的哺乳动物中至少一种IL-16介导的生物活性的停止。 本发明提供了用于治疗与诸如例如人类的哺乳动物中的疾病状态如哮喘,类风湿性关节炎,炎症性肠病(IBD)和系统性红斑狼疮(SLE)相关的炎症的方法和组合物。
    • 2. 发明授权
    • IL-16 antagonists
    • IL-16拮抗剂
    • US06723697B2
    • 2004-04-20
    • US09929922
    • 2001-08-15
    • David M. CenterWilliam W. CruikshankHardy Kornfeld
    • David M. CenterWilliam W. CruikshankHardy Kornfeld
    • A61K3800
    • 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,优选衍生自CD4的肽。 这些肽具有IL-16拮抗性质,包括选择性结合IL-16并抑制IL-16介导的生物活性的能力。 肽包含天然人CD4受体的特定部分及其变体,因此在给予人时是非免疫原性的。 本发明还提供含有至少一种IL-16拮抗剂肽的组合物,其可以抑制,抑制或引起包括人在内的哺乳动物中至少一种IL-16介导的生物活性的停止。 本发明提供了用于治疗与诸如例如人类的哺乳动物中的疾病状态如哮喘,类风湿性关节炎,炎症性肠病(IBD)和系统性红斑狼疮(SLE)相关的炎症的方法和组合物。