JCV NEUTRALIZING ANTIBODIES
    72.
    发明申请
    JCV NEUTRALIZING ANTIBODIES 有权
    JCV中和抗体

    公开(公告)号:US20150050271A1

    公开(公告)日:2015-02-19

    申请号:US14386262

    申请日:2013-03-15

    Abstract: In one aspect, the disclosure provides neutralizing antibodies against JCV and methods for the treatment of PML. In some embodiments, aspects of the invention relate to an isolated JC-vims neutralizing monoclonal antibody against JCV capsid protein VPI (JCV-VP1). In some embodiments, the antibody suppresses infectivity of the JC-vims. In some embodiments, the antibody binds the sialic acid binding pocket of JCV-VP1.

    Abstract translation: 一方面,本公开提供了针对JCV的中和抗体和用于治疗PML的方法。 在一些实施方案中,本发明的方面涉及针对JCV衣壳蛋白VPI(JCV-VP1)的分离的JC-vim中和单克隆抗体。 在一些实施方案中,抗体抑制JC-vims的感染性。 在一些实施方案中,抗体结合JCV-VP1的唾液酸结合口袋。

    Neuroprotection in Demyelinating Diseases
    73.
    发明申请
    Neuroprotection in Demyelinating Diseases 审中-公开
    神经保护脱髓鞘疾病

    公开(公告)号:US20140323570A1

    公开(公告)日:2014-10-30

    申请号:US14264653

    申请日:2014-04-29

    Inventor: Ralf GOLD

    CPC classification number: A61K31/225

    Abstract: Methods of treating neurological disorders characterized by extensive demyelination and/or axonal loss are provided. Examples of such disorders include secondary progressive multiple sclerosis and Devic's disease. The disclosed methods include administering to a subject having such a disorder a therapeutically effective amount of, for example, dimethyl fumarate or monomethyl fumarate.

    Abstract translation: 提供治疗以广泛脱髓鞘和/或轴突损失为特征的神经障碍的方法。 这种病症的实例包括继发性进行性多发性硬化症和Devic氏病。 所公开的方法包括向具有这种病症的受试者施用治疗有效量的例如富马酸二甲酯或富马酸单甲酯。

    Sp35 Antibodies and Uses Thereof
    76.
    发明申请
    Sp35 Antibodies and Uses Thereof 有权
    Sp35抗体及其用途

    公开(公告)号:US20130336991A1

    公开(公告)日:2013-12-19

    申请号:US13841351

    申请日:2013-03-15

    Abstract: Endogenous Sp35 is a negative regulator for neuronal survival, axon regeneration, oligodendrocyte differentiation and myelination (Negative Regulator). Molecules that block endogenous Sp35 function, such anti-Sp35 antibodies can be used as therapeutics for the treatment of neuron and oligodendrocyte dysfunction. The present invention provides antibodies specific for Sp35, and methods of using such antibodies as antagonists of endogenous Sp35 function. The invention further provides specific hybridoma and phage library-derived monoclonal antibodies, nucleic acids encoding these antibodies, and vectors and host cells comprising these antibodies. The invention further provides methods of promoting oligodendrocyte survival and myelination in a vertebrate, comprising administering to a vertebrate in need of such treatment an effective amount of an anti-Sp35 antibody

    Abstract translation: 内源性Sp35是神经元存活,轴突再生,少突胶质细胞分化和髓鞘形成(负调节因子)的负调节因子。 阻断内源性Sp35功能的分子,这种抗Sp35抗体可以用作治疗神经元和少突胶质细胞功能障碍的治疗剂。 本发明提供对Sp35特异性的抗体,以及使用抗体作为内源性Sp35功能拮抗剂的方法。 本发明还提供特异性杂交瘤和源自噬菌体文库的单克隆抗体,编码这些抗体的核酸,以及包含这些抗体的载体和宿主细胞。 本发明进一步提供了在脊椎动物中促进少突胶质细胞存活和髓鞘形成的方法,包括向需要这种治疗的脊椎动物施用有效量的抗Sp35抗体

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