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    • 3. 发明申请
    • PIKE-A ENHANCES INFECTION BY MYXOMA VIRUS
    • PIKE-A通过MYXOMA病毒增强感染
    • WO2007143538A3
    • 2008-02-21
    • PCT/US2007070199
    • 2007-06-01
    • ROBARTS RES INSTMCFADDEN GRANTWERDEN STEVEN
    • MCFADDEN GRANTWERDEN STEVEN
    • C12N15/00
    • A61K35/76A61K38/46C12Y306/05A61K2300/00
    • Cellular Akt activation is increased by transducing an Akt-containing cell with a vector that expresses exogenous PIKE-A (PIl 3 -kinase enhancer activating Akt) in the cell. Expression of PIKE-A increases the susceptibility of cancer cells to myxoma virus infection. Cancer is treated by administering a vector that infects cancer cells and expresses exogenous PIKE-A; and a myxoma virus. Cancer is treated by taking cancer cells from a subject, transducing them ex vivo with a vector that expresses exogenous PIKE-A in the cells, treating the transduced cells with a myxoma virus, and then returning the transduced cells to the subject. Alternatively, myxoma virus can be administered to the patient after the transduced cells have been returned to the patient. The susceptibility of cells to infection with a myxoma virus can be determined by assaying for PIKE-A expression. Cellular expression of PIKE-A in the cell indicates susceptibility to myxoma virus infection.
    • 通过用表达外源PIKE-A(PI3-3激酶增强子激活Akt)的载体转导含Akt的细胞来增加细胞Akt活化。 PIKE-A的表达增加了癌细胞对粘液瘤病毒感染的敏感性。 通过施用感染癌细胞并表达外源性PIKE-A的载体来治疗癌症; 和粘液瘤病毒。 通过从受试者中摄取癌细胞来治疗癌症,用在细胞中表达外源性PIKE-A的载体离体转染它们,用粘液瘤病毒处理转导的细胞,然后将转导的细胞返回到受试者。 或者,在转导的细胞已经返回到患者之后,可以向患者施用粘液瘤病毒。 可以通过测定PIKE-A表达来确定细胞对粘液瘤病毒感染的易感性。 细胞中PIKE-A的细胞表达表明对粘液瘤病毒感染的敏感性。
    • 6. 发明申请
    • M11L DERIVED PEPTIDES AND THERAPEUTIC USE THEREOF
    • M11L衍生的肽及其治疗用途
    • WO2004106370A1
    • 2004-12-09
    • PCT/EP2004/006581
    • 2004-05-28
    • THERAPTOSIS SAROBARTS RESEARCH INSTITUTEJACOTOT, EtienneMCFADDEN, Grant
    • JACOTOT, EtienneMCFADDEN, Grant
    • C07K14/47
    • C07K14/005A61K38/00C07K2319/00C12N2710/24022
    • This invention relates to a novel chimeric peptide derived from M11L protein of myxoma poxvirus capable of inhibiting apoptosis and its use as a cytoprotective molecule, as well as to pharmaceutical compositions containing the M11L derived chimeric peptides. Also provided are nucleic acid molecules that encode the chimeric anti-apoptotic peptides, and methods for using the proteins and nucleic acid molecules as cytoprotective molecules. The present invention further relates to a M11L fusion peptide possessing an uptake action and/or a targeted moiety into and to a cell and its use as apoptosis inhibitor. The M11L derived peptides and fusions peptides are useful for treating AIDS, neurodegenerative diseases, osteomyelodysplasia, ischemic diseases, infectious multiple organ failure, hepatitis, ischemic reperfusion disorders, diabetes and the like.
    • 本发明涉及能够抑制凋亡的粘液瘤痘病毒的M11L蛋白的新型嵌合肽及其作为细胞保护分子的用途,以及含有M11L衍生的嵌合肽的药物组合物。 还提供编码嵌合抗凋亡肽的核酸分子,以及使用蛋白质和核酸分子作为细胞保护分子的方法。 本发明还涉及具有吸收作用和/或靶向部分进入细胞和细胞的M11L融合肽及其作为细胞凋亡抑制剂的用途。 M11L衍生肽和融合肽可用于治疗AIDS,神经变性疾病,骨髓发育不良,缺血性疾病,感染性多器官功能衰竭,肝炎,缺血再灌注障碍,糖尿病等。
    • 8. 发明申请
    • VIRAL SERPIN REGULATION OF INFLAMATION
    • VIRAL SERPIN调节爆发
    • WO2004039391A1
    • 2004-05-13
    • PCT/CA2003/001682
    • 2003-10-31
    • LUCAS, Alexandra, R.MCFADDEN, Grant, D.
    • LUCAS, Alexandra, R.MCFADDEN, Grant, D.
    • A61K38/03
    • A61K38/55
    • The present invention provides for a pharmaceutical composition containing at least one compound that promotes intracellular signalling via the human urokinase plasminogen activator receptor. The compound binds the human urokinase plasminogen activator receptor, the compound binds one or more intracellular protein(s) directly or indirectly associated with intracellular signalling via human urokinase plasminogen activator receptor, and the compound binds one or more intracellular protein(s) that are modulated by urokinase plasminogen activator receptor activity. The compound is an organic or inorganic compound with a molecular weight less than 1kDa, compound is a peptide between 2 and 20 amino acids in length, and the compound is a polypeptide greater than 20 amino acids in length. The compound is an antibody or fragment thereof, the compound is a nucleic acid, and the compound is administered to humans in vivo , and to human cells ex vivo . The composition includes a pharmaceutically acceptable carrier, and the composition is administered to a human individual for the treatment of an inflamatory condition.
    • 本发明提供含有至少一种通过人尿激酶纤溶酶原激活物受体促进细胞内信号传导的化合物的药物组合物。 该化合物结合人尿激酶纤溶酶原激活物受体,该化合物通过人尿激酶纤溶酶原激活物受体直接或间接地与细胞内信号传导相关联的一种或多种细胞内蛋白质,并且该化合物结合调节的一种或多种细胞内蛋白质 通过尿激酶纤溶酶原激活物受体活性。 该化合物是分子量小于1kDa的有机或无机化合物,化合物是长度在2至20个氨基酸之间的肽,并且化合物是长度大于20个氨基酸的多肽。 化合物是抗体或其片段,化合物是核酸,并且化合物在体内施用于人体,并且离体施用于人类细胞。 组合物包括药学上可接受的载体,并且将组合物施用于人个体以治疗炎症状况。