Modulation of T cell differentiation for the treatment of T helper cell mediated diseases
    8.
    发明授权
    Modulation of T cell differentiation for the treatment of T helper cell mediated diseases 有权
    调节T细胞分化治疗T辅助细胞介导的疾病

    公开(公告)号:US07393532B1

    公开(公告)日:2008-07-01

    申请号:US10088950

    申请日:2000-10-18

    IPC分类号: A61K39/395 A61K39/00

    摘要: The present invention relates to methods for the treatment and diagnosis of immune related diseases, including those mediated by cytokines released primarily either Th1 or Th2 cells in response to antigenic stimulation. The present invention further relates to methods for biasing the differentiation of T-cells in either the Th1 subtype or the Th2 subtype, based on the relative expression levels of the gene TCCR, and its agonists or antagonists. The present invention further relates to a method of diagnosing Th1- and Th2-mediated diseases.

    摘要翻译: 本发明涉及用于治疗和诊断免疫相关疾病的方法,包括由主要以Th1或Th2细胞响应于抗原刺激释放的细胞因子介导的那些。 本发明还涉及基于TCCR及其激动剂或拮抗剂的相对表达水平来偏置Th1亚型或Th2亚型中T细胞分化的方法。 本发明还涉及诊断Th1-和Th2介导的疾病的方法。

    Engineered TAA antibody-TNFSF member ligand fusion molecules
    10.
    发明授权
    Engineered TAA antibody-TNFSF member ligand fusion molecules 有权
    工程TAA抗体-TNFSF成员配体融合分子

    公开(公告)号:US09534056B2

    公开(公告)日:2017-01-03

    申请号:US14124565

    申请日:2012-06-06

    摘要: The field of the present invention relates to genetically engineered fusion molecules, methods of making said fusion molecules, and uses thereof in anti-tumor immunotherapies. More specifically, the present invention relates to engineered fusion molecules comprising an antibody (Ab) which can target tumor cells (e.g., RITUXIN®), fused to one or more biologic moieties capable of inducing apoptosis in tumor cells, e.g., tumor necrosis factor super family (TNFSF) member ligands such as TNF-α, CD40L, CD95L (also “FasL/Apo-1L”) and TRAIL/Apo-2L. Importantly, the engineered fusion molecules of the present invention retain the death-inducing properties of the biologic moiety at optimum concentrations and with reduced systemic toxicities.

    摘要翻译: 本发明的领域涉及基因工程融合分子,制备所述融合分子的方法及其在抗肿瘤免疫治疗中的用途。 更具体地,本发明涉及包含能够靶向肿瘤细胞的抗体(Ab)的工程化融合分子,所述抗体(例如RITUXIN?)与一个或多个能诱导肿瘤细胞凋亡的生物部分融合,例如肿瘤坏死因子超级 家族(TNFSF)成员配体如TNF-α,CD40L,CD95L(也称为“FasL / Apo-1L”)和TRAIL / Apo-2L。 重要的是,本发明的工程改造的融合分子将生物部位的死亡诱导性质保持在最佳浓度和降低的全身毒性。