PCA3, PCA3 Genes, and Methods of Use
    59.
    发明申请
    PCA3, PCA3 Genes, and Methods of Use 审中-公开
    PCA3,PCA3基因和使用方法

    公开(公告)号:US20170073776A1

    公开(公告)日:2017-03-16

    申请号:US15364962

    申请日:2016-11-30

    Abstract: The present invention relates, in general, to a prostate-specific antigen, PCA3. In particular, the present invention relates to nucleic acid molecules coding for the PCA3 protein; purified PCA3 proteins and polypeptides; recombinant nucleic acid molecules; cells containing the recombinant nucleic acid molecules; antibodies having binding affinity specifically to PCA3 proteins and polypeptides; hybridomas containing the antibodies; nucleic acid probes for the detection of nucleic acids encoding PCA3 proteins; a method of detecting nucleic acids encoding PCA3 proteins or polypeptides in a sample; kits containing nucleic acid probes or antibodies; bioassays using the nucleic acid sequence, protein or antibodies of this invention to diagnose, assess, or prognose a mammal afflicted with prostate cancer; therapeutic uses; and methods of preventing prostate cancer in an animal.

    Abstract translation: 本发明一般涉及前列腺特异性抗原PCA3。 特别地,本发明涉及编码PCA3蛋白的核酸分子; 纯化的PCA3蛋白和多肽; 重组核酸分子; 含有重组核酸分子的细胞; 具有与PCA3蛋白和多肽特异性结合亲和力的抗体; 含有抗体的杂交瘤; 用于检测编码PCA3蛋白质的核酸的核酸探针; 检测样品中编码PCA3蛋白或多肽的核酸的方法; 含有核酸探针或抗体的试剂盒; 使用本发明的核酸序列,蛋白质或抗体的生物测定来诊断,评估或预测患有前列腺癌的哺乳动物; 治疗用途; 以及预防动物中前列腺癌的方法。

    Methods for the treatment or prevention of systemic sclerosis
    60.
    发明授权
    Methods for the treatment or prevention of systemic sclerosis 有权
    治疗或预防系统性硬化症的方法

    公开(公告)号:US09259466B2

    公开(公告)日:2016-02-16

    申请号:US14471968

    申请日:2014-08-28

    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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