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PHARMACODYNAMIC MARKERS INDUCED BY ALPHA INTERFERON2009125616 12/06/2006

机译:ALPHA干扰素诱导的药代动力学标记2009125616 12/06/2006

摘要

1. A method of treating a patient with a disease or disorder mediated by interferon type I (IFN type I) or interferon alpha (IFNα), comprising: introducing an agent that binds and modulates the action of IFN type I or IFNα, wherein the patient includes an expression profile of PD markers, induced IFN type I or IFNα; and said agent neutralizes the expression profile of PD markers induced by IFN type I or IFNα in a patient. 2. The method of claim 1, further comprising detecting a neutralization of the expression profile of PD markers induced by type I IFN or IFNα in a patient. The method of claim 1, wherein the expression profile of the PD markers induced by IFN type I or IFNα includes upregulating the expression or action of the MX1, LY6E, IFI27, OAS1 IFIT1, IFI6, IFI44L, ISG15, LAMP3, OASL, RSAD2 and IFI44 genes. four. The method of claim 1, wherein the agent is a biological agent. The method of claim 4, wherein the agent is an antibody. The method of claim 5, wherein the antibody is a MEDI-545.7 antibody. The method of claim 5, wherein the antibody is specific for one or more IFN type I or IFNα subtypes, but is not a MEDI-545.8 antibody. The method of claim 1, wherein administering the agent alleviates one or more symptoms of the disease or disorder. The method of claim 5, wherein the antibody is administered at a dose of about 0.03-30 mg / kg. The method of claim 9, wherein the antibody is administered at a dose of about 0.3-3 mg / kg. The method of claim 10, wherein the antibody is administered at a dose of 0.03-1 mg / kg. The method according to one of paragraphs. 9-11, in which the agent neutralizes the expression profile of PD markers induced by type I IFN or IFNα in a patient by at least 10% .13. The method of claim 12, wherein the agent neutralizes the expression profile of PD markers induced by type I IFN or IF�
机译:1.一种治疗由I型干扰素(I型干扰素)或α干扰素(IFNα)介导的疾病或病症的患者的方法,其包括:引入结合并调节I型干扰素或IFNα作用的药剂,其中患者包括PD标志物,诱导的I型IFN或IFNα的表达谱;所述药物中和患者中由I型IFN或IFNα诱导的PD标志物的表达谱。 2.根据权利要求1所述的方法,其进一步包括检测患者中由I型IFN或IFNα诱导的PD标志物的表达谱的中和。 2.根据权利要求1所述的方法,其中,由I型IFN或IFNα诱导的PD标志物的表达谱包括上调MX1,LY6E,IFI27,OAS1,IFIT1,IFI6,IFI44L,ISG15,LAMP3,OASL,RSAD2和IFI44基因。四。 2.根据权利要求1所述的方法,其中,所述试剂是生物试剂。 5.根据权利要求4所述的方法,其中,所述试剂是抗体。 6.根据权利要求5所述的方法,其中所述抗体是MEDI-545.7抗体。 6.根据权利要求5所述的方法,其中所述抗体对一种或多种I型IFN或IFNα亚型具有特异性,但不是MEDI-545.8抗体。 2.根据权利要求1所述的方法,其中施用所述试剂减轻所述疾病或病症的一种或多种症状。 6.权利要求5的方法,其中所述抗体以约0.03-30mg / kg的剂量施用。 10.根据权利要求9所述的方法,其中以约0.3-3mg / kg的剂量施用所述抗体。 11.根据权利要求10所述的方法,其中以0.03-1mg / kg的剂量施用所述抗体。根据段落之一的方法。 9-11,其中该药物中和患者中由I型IFN或IFNα诱导的PD标志物的表达谱至少10%.13。 13.根据权利要求12所述的方法,其中所述试剂中和由I型IFN或IF诱导的PD标志物的表达谱。

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