GALACTOSAMINOGALACTAN COMPRISING alpha-1-4 LINKED GALACTOSE AND alpha-1-4 LINKED N-ACETYLGALACTOSAMINE FOR USE IN THE TREATMENT OF AT LEAST ONE INFLAMMATORY DISEASE
    41.
    发明申请
    GALACTOSAMINOGALACTAN COMPRISING alpha-1-4 LINKED GALACTOSE AND alpha-1-4 LINKED N-ACETYLGALACTOSAMINE FOR USE IN THE TREATMENT OF AT LEAST ONE INFLAMMATORY DISEASE 审中-公开
    包含α-1-4连接的胶质糖和α-1-4连接的N-乙酰胆碱酯酶用于治疗至少一种炎症性疾病的糖皮质激素

    公开(公告)号:US20160008391A1

    公开(公告)日:2016-01-14

    申请号:US14760604

    申请日:2014-01-14

    CPC classification number: A61K31/715 A61K31/726 A61K45/06

    Abstract: A first object of the invention is galactosaminogalactan comprising α1-4 linked galactose, α1-4 linked N-acetylgalactosamine, and optionally α1-4 linked galactosamine, for use in the treatment of at least one inflammatory disease. Another object of the invention is a pharmaceutical composition comprising a galactosaminogalactan comprising α1-4 linked galactose, α1-4 linked N-acetylgalactosamine, and optionally α1-4 linked galactosamine, as defined herein, and optionally a pharmaceutically acceptable carrier. Another object of the invention is a pharmaceutical composition according to the invention, for use in the treatment of at least one inflammatory disease. Another object of the invention is an inhibitor of IL-1RA for use in the treatment of human fungal diseases. Another object of the invention is a pharmaceutical composition comprising an inhibitor of IL-1RA, and optionally a pharmaceutically acceptable carrier.

    Abstract translation: 本发明的第一个目的是包含α1-4连接的半乳​​糖,α1-4连接的N-乙酰半乳糖胺和任选α1-4连接的半乳​​糖胺的半乳糖胺半乳聚糖,用于治疗至少一种炎性疾病。 本发明的另一个目的是一种药物组合物,其包含含有α1-4连接的半乳​​糖,α1-4连接的N-乙酰半乳糖胺和任选地α1-4连接的半乳​​糖胺,如本文所定义的任选的药物可接受载体的半乳糖胺半乳聚糖。 本发明的另一个目的是根据本发明的药物组合物,用于治疗至少一种炎性疾病。 本发明的另一个目的是用于治疗人类真菌疾病的IL-1RA抑制剂。 本发明的另一个目的是一种药物组合物,其包含IL-1RA的抑制剂和任选的药学上可接受的载体。

    METHODS FOR THE TREATMENT OR PREVENTION OF SYSTEMIC SCLEROSIS
    42.
    发明申请
    METHODS FOR THE TREATMENT OR PREVENTION OF SYSTEMIC SCLEROSIS 有权
    治疗或预防系统性溃疡的方法

    公开(公告)号:US20130287794A1

    公开(公告)日:2013-10-31

    申请号:US13928557

    申请日:2013-06-27

    Abstract: The invention is in the field of molecular immunology, more in particular, in the field of the prevention or treatment of autoimmune diseases, more in particular, systemic sclerosis or scleroderma. The invention is based on the observation that SSC patients have an elevated plasma level of CXCL4. This was found to contribute to the pathogenesis of SSc, in particular, fibrosis. When CXCL4 was neutralized in in vitro experiments, the fibrotic effects could be neutralized. This led us to conclude that SSc may be cured by reducing the plasma level of CXCL4. The invention, therefore, relates to a method for treatment or prevention of fibrosis in patients with scleroderma, wherein the plasma level of CXCL4 is reduced.

    Abstract translation: 本发明涉及分子免疫学领域,特别是在预防或治疗自身免疫性疾病领域,特别是系统性硬化症或硬皮病领域。 本发明是基于SSC患者血浆CXCL4水平升高的观察。 这被发现有助于SSc的发病机制,特别是纤维化。 当CXCL4在体外实验中被中和时,可以中和纤维化作用。 这导致我们得出结论,通过降低CXCL4的血浆水平可以治愈SSc。 因此,本发明涉及用于治疗或预防硬皮病患者纤维化的方法,其中CXCL4的血浆水平降低。

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