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    • 1. 发明申请
    • TRPM2-specfic inhibitors
    • TRPM2特异性抑制剂
    • US20080114079A1
    • 2008-05-15
    • US11652265
    • 2007-01-10
    • Frances E. LundSantiago Partida-SanchezTim Walseth
    • Frances E. LundSantiago Partida-SanchezTim Walseth
    • A61K47/00C12N5/06C12Q1/02A61P9/00A61P1/00A61P19/00
    • C07K14/705A61K31/365G01N33/6872G01N2500/04
    • The present invention relates to methods and compositions for modulating ADPR-mediated migratory activity of cells through regulation of the TRPM2 cation channel. Such methods and compositions may be used for the treatment of disorders including, but not limited to, inflammation, ischemia, atherosclerosis, asthma, autoimmune disease, diabetes, arthritis, allergies, and transplant rejection. Such cells include, for example, neutrophils, lymphocytes, eosinophils, macrophages, monocytes and dendritic cells. The invention further relates to specific inhibition of TRPM2 by blocking the activity of ADPR. The invention also relates to drug screening assays designed to identify compounds that regulate TRPM2 and thereby also function to modulate ADPR-mediated cell migration. The invention is based on the discovery that, 8Br-ADPR, which specifically inhibits activation of TRPM2, acts to inhibit ADPR-mediated cell migration.
    • 本发明涉及通过调节TRPM2阳离子通道调节ADPR介导的细胞迁移活性的方法和组合物。 这些方法和组合物可用于治疗疾病,包括但不限于炎症,缺血,动脉粥样硬化,哮喘,自身免疫性疾病,糖尿病,关节炎,过敏反应和移植排斥。 这样的细胞包括例如嗜中性粒细胞,淋巴细胞,嗜酸性粒细胞,巨噬细胞,单核细胞和树突状细胞。 本发明还涉及通过阻断ADPR的活性而对TRPM2的特异性抑制。 本发明还涉及设计用于鉴定调节TRPM2的化合物并由此也可用于调节ADPR介导的细胞迁移的药物筛选测定。 本发明基于以下发现:特异性抑制TRPM2激活的8Br-ADPR起抑制ADPR介导的细胞迁移的作用。
    • 3. 发明授权
    • SM38 nucleic acid molecules
    • SM38核酸分子
    • US07695933B2
    • 2010-04-13
    • US11058924
    • 2005-02-15
    • Frances E. LundTroy D. RandallSantiago Partida-Sanchez
    • Frances E. LundTroy D. RandallSantiago Partida-Sanchez
    • C12P21/06C12N1/20C12N15/63C07H21/04
    • C07K14/4354C12N9/2497C12Y302/02005
    • The present invention relates to methods for modulating the migratory activity of cells expressing CD38 for the treatment of disorders including, but not limited to, inflammation, ischemia, asthma, autoimmune disease, diabetes, arthritis, allergies, infection with pathogenic organisms, such as parasites, and transplant rejection. Such cells include, for example, neutrophils, lymphocytes, eosinophils, macrophages and dentritic cells. The invention further relates to drug screening assays designed to identify compounds that modulate the ADP-ribosyl cyclase activity of CD38 and the use of such compounds in the treatment of disorders involving CD38 modulated cell migration. Additionally, the invention relates to the isolation and characterization of a CD38 homologue from the parasitic flatworm, Schistosoma mansoni.
    • 本发明涉及调节表达CD38的细胞的迁移活性的方法,用于治疗疾病,包括但不限于炎症,局部缺血,哮喘,自身免疫疾病,糖尿病,关节炎,过敏,病原体感染等寄生虫 ,移植排斥。 这样的细胞包括例如嗜中性粒细胞,淋巴细胞,嗜酸性粒细胞,巨噬细胞和牙髓细胞。 本发明还涉及设计用于鉴定调节CD38的ADP-核糖基环化酶活性的化合物的药物筛选试验,以及这些化合物在治疗涉及CD38调节的细胞迁移的疾病中的用途。 此外,本发明涉及从寄生扁丝虫曼氏血吸虫分离和表征CD38同系物。
    • 4. 发明授权
    • CD38 modulated chemotaxis
    • CD38调节趋化性
    • US08084035B2
    • 2011-12-27
    • US12703062
    • 2010-02-09
    • Frances E. LundTroy D. RandallSantiago Partida-Sanchez
    • Frances E. LundTroy D. RandallSantiago Partida-Sanchez
    • A61K39/00A61K39/385G01N33/53C07K14/52
    • C07K14/4354C12N9/2497C12Y302/02005
    • The present invention relates to methods for modulating the migratory activity of cells expressing CD38 for the treatment of disorders including, but not limited to, inflammation, ischemia, asthma, autoimmune disease, diabetes, arthritis, allergies, infection with pathogenic organisms, such as parasites, and transplant rejection. Such cells include, for example, neutrophils, lymphocytes, eosinophils, macrophages and dentritic cells. The invention further relates to drug screening assays designed to identify compounds that modulate the ADP-ribosyl cyclase activity of CD38 and the use of such. compounds in the treatment of disorders involving CD38 modulated cell migration. Additionally, the invention relates to the isolation and characterization of a CD38 homologue from the parasitic flatworm, Schistosoma mansoni.
    • 本发明涉及调节表达CD38的细胞的迁移活性的方法,用于治疗疾病,包括但不限于炎症,局部缺血,哮喘,自身免疫疾病,糖尿病,关节炎,过敏,病原体感染等寄生虫 ,移植排斥。 这样的细胞包括例如嗜中性粒细胞,淋巴细胞,嗜酸性粒细胞,巨噬细胞和牙髓细胞。 本发明还涉及设计用于鉴定调节CD38的ADP-核糖基环化酶活性的化合物的药物筛选测定及其用途。 治疗涉及CD38调节细胞迁移的疾病的化合物。 此外,本发明涉及从寄生扁丝虫曼氏血吸虫分离和表征CD38同系物。
    • 6. 发明授权
    • Methods for identifying compounds that inhibit CD38 activity
    • 鉴定抑制CD38活性的化合物的方法
    • US06955884B2
    • 2005-10-18
    • US09982616
    • 2001-10-17
    • Frances E. LundTroy D. RandallSantiago Partida-Sánchez
    • Frances E. LundTroy D. RandallSantiago Partida-Sánchez
    • G01N33/50C07K14/435C07K16/40C12N1/15C12N1/19C12N1/21C12N5/10C12N9/00C12N9/24C12N15/09C12Q1/02C12Q1/25G01N33/15G01N33/53G01N33/566G01N33/573C12N5/00C12N5/02
    • C07K14/4354C12N9/2497C12Y302/02005
    • The present invention relates to methods for modulating the migratory activity of cells expressing CD38 for the treatment of disorders including, but not limited to, inflammation, ischemia, asthma, autoimmune disease, diabetes, arthritis, allergies, infection with pathogenic organisms and transplant rejection. Such cells include, for example, neutrophils, lymphocytes, eosinophils, macrophages and dentritic cells. The invention further relates to drug screening assays designed to identify compounds that modulate the ADP-ribosyl cyclase activity of CD38 and the use of such compounds in the treatment of disorders involving CD38 modulated cell migration. The invention is based on the discovery that CD38 ADP-ribosyl cyclase activity is required for chemotaxis. Furthermore, the invention relates to methods for identifying compounds that modulate the enzyme activity of the S. mansoni CD38 homologue and using those compounds in the treatment of pathologic disorders caused by helminth infection. This is based on the discovery that helminths such as S. mansoni express CD38 homologues.
    • 本发明涉及调节表达CD38的细胞的迁移活性的方法,用于治疗疾病,包括但不限于炎症,局部缺血,哮喘,自身免疫疾病,糖尿病,关节炎,过敏,病原体感染和移植排斥。 这样的细胞包括例如嗜中性粒细胞,淋巴细胞,嗜酸性粒细胞,巨噬细胞和牙髓细胞。 本发明还涉及设计用于鉴定调节CD38的ADP-核糖基环化酶活性的化合物的药物筛选试验,以及这些化合物在治疗涉及CD38调节的细胞迁移的疾病中的用途。 本发明基于发现趋化性所需的CD38 ADP-核糖基环化酶活性。 此外,本发明涉及用于鉴定调节曼氏血清CD38同源物的酶活性并使用这些化合物治疗由蠕虫感染引起的病理性疾病的化合物的方法。 这是基于以下发现:蠕虫如曼氏男性表达CD38同源物。