Synthetic analogs of sphingolipids
    2.
    发明授权
    Synthetic analogs of sphingolipids 有权
    鞘脂的合成类似物

    公开(公告)号:US08962891B2

    公开(公告)日:2015-02-24

    申请号:US12742045

    申请日:2008-11-09

    Abstract: The present invention provides new ceramide analogs indicated as the compounds of formula (II). These novel analogs exhibit a significant anti cancerous effect and are therefore provided as a pharmaceutical composition for treating cell proliferative diseases, neurodegenerative disorders, metabolism-associated conditions, infectious diseases, and immune-related disorders. The invention further provides combined compositions and kits combining the novel ceramide analogs of formula (II) with an additional therapeutic agent.

    Abstract translation: 本发明提供了新的表示为式(II)化合物的神经酰胺类似物。 这些新型类似物表现出显着的抗癌作用,因此作为治疗细胞增殖性疾病,神经变性疾病,代谢相关病症,感染性疾病和免疫相关疾病的药物组合物提供。 本发明还提供组合的组合物和试剂盒,其将式(II)的新型神经酰胺类似物与另外的治疗剂组合。

    METHODS, SYSTEMS, AND COMPOSITIONS FOR NEURONAL DIFFERENTIATION OF MULTIPOTENT STROMAL CELLS
    3.
    发明申请
    METHODS, SYSTEMS, AND COMPOSITIONS FOR NEURONAL DIFFERENTIATION OF MULTIPOTENT STROMAL CELLS 有权
    用于多重结构细胞神经元分化的方法,系统和组合物

    公开(公告)号:US20120148550A1

    公开(公告)日:2012-06-14

    申请号:US13377558

    申请日:2010-06-10

    Abstract: Some embodiments of the invention comprise methods, systems, and compositions to selectively induce, whether in vitro or in vivo, the neuronal differentiation of multipotent stromal cells through the application of microRNAs, including but not limited to miRNA-124, miRNA-137 and/or miRNA-9* expression products of those miRNAs, and molecules and compositions containing functional elements of those miRNAs. Some embodiments of the invention also comprise the therapeutic administration and use of such induced cells to treat mammalian injuries and diseases, including but not limited to, nervous system injuries or diseases that may otherwise result in decreased cell or system function.

    Abstract translation: 本发明的一些实施方案包括方法,系统和组合物,其通过应用微小RNA(包括但不限于miRNA-124,miRNA-137和/或核糖体)选择性地诱导多潜能基质细胞的体外或体内神经元分化, 或miRNA-9 *表达产物,以及含有这些miRNA功能元件的分子和组合物。 本发明的一些实施方案还包括治疗性施用和使用这种诱导的细胞来治疗哺乳动物的损伤和疾病,包括但不限于神经系统损伤或可能导致细胞或系统功能降低的疾病。

    Non-myeloablative tolerogenic treatment

    公开(公告)号:US06447767B1

    公开(公告)日:2002-09-10

    申请号:US09506082

    申请日:2000-02-16

    Abstract: The present invention features a method of inducing donor-specific tolerance in a host. Tolerogenic treatments of the present invention may be administered to a host prior to transplantation of donor-derived materials. The tolerogenic treatment involves (1) administering an immunosuppressive agent to a host mammal in a non-myeloablative regimen sufficient to decrease, but not necessarily to eliminate, the host mammal's functional T lymphocyte population; (2) infusing donor antigens from a non-syngeneic donor into the host mammal; (3) eliminating those host T lymphocytes responding to the infused donor antigens using a non-myeloablative dose of lymphocytotoxic or tolerizing agent; and (4) administering donor hematopoietic cells to the host mammal. Donor lymphoid cells used for cell therapy of a host mammal can be depleted of host specific immunological reactivity by methods essentially similar to those use for tolerizing a host mammal prior to transplantation.

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