Method for identifying immune response modulators
    2.
    发明授权
    Method for identifying immune response modulators 有权
    识别免疫反应调节剂的方法

    公开(公告)号:US08846308B2

    公开(公告)日:2014-09-30

    申请号:US12663635

    申请日:2008-06-06

    CPC classification number: G01N33/6872 G01N2500/00

    Abstract: Methods of identifying immune response modulators are disclosed. Some methods comprise identifying chemical candidates that modulate oligomerization of FOXP3 and/or fragments thereof comprising the Zinc-LeuZip domains. Some methods comprise identifying chemical candidates that modulate the hetero-oligomerization of FOXP1 with FOXP3 and/or fragments thereof comprising the Zinc-LeuZip domains. Some methods comprise identifying chemical candidates that modulate interaction of IL-2 promoter with FOXP3 and/or fragments thereof comprising the Zinc-LeuZip domains. Method of treating individuals who have or are suspected of having autoimmune disease, inflammatory disease, cell, tissue or organ transplantation, or coronary artery disease, and methods of treating individuals who have or are suspected of having infectious disease, cancer, or who are immunocompromised or undergoing vaccination are disclosed.

    Abstract translation: 公开了鉴定免疫应答调节剂的方法。 一些方法包括鉴定调节FOXP3和/或其包含Z-LeuZip结构域的片段的寡聚化的化学候选物。 一些方法包括鉴定用FOXP3调节FOXP1的异源寡聚化的化学候选物和/或其包含Z-LeuZip结构域的片段。 一些方法包括鉴定调节IL-2启动子与FOXP3和/或其包含Zinc-LeuZip结构域的片段的相互作用的化学候选物。 治疗患有或怀疑患有自身免疫疾病,炎性疾病,细胞,组织或器官移植或冠状动脉疾病的个体的方法,以及治疗患有或怀疑患有感染性疾病,癌症或免疫受损的个体的方法 或接受疫苗接种。

    FOXP3 OLIGOMERIZATION AND INTERMOLECULAR INTERACTIONS
    4.
    发明申请
    FOXP3 OLIGOMERIZATION AND INTERMOLECULAR INTERACTIONS 有权
    FOXP3低分子化和分子间相互作用

    公开(公告)号:US20110124560A1

    公开(公告)日:2011-05-26

    申请号:US12663635

    申请日:2008-06-06

    CPC classification number: G01N33/6872 G01N2500/00

    Abstract: Methods of identifying immune response modulators are disclosed. Some methods comprise identifying chemical candidates that modulate oligomerization of FOXP3 and/or fragments thereof comprising the Zinc-LeuZip domains. Some methods comprise identifying chemical candidates that modulate the hetero-oligomerization of FOXP1 with FOXP3 and/or fragments thereof comprising the Zinc-LeuZip domains. Some methods comprise identifying chemical candidates that modulate interaction of IL-2 promoter with FOXP3 and/or fragments thereof comprising the Zinc-LeuZip domains. Method of treating individuals who have or are suspected of having autoimmune disease, inflammatory disease, cell, tissue or organ transplantation, or coronary artery disease, and methods of treating individuals who have or are suspected of having infectious disease, cancer, or who are immunocompromised or undergoing vaccination are disclosed.

    Abstract translation: 公开了鉴定免疫应答调节剂的方法。 一些方法包括鉴定调节FOXP3和/或其包含Z-LeuZip结构域的片段的寡聚化的化学候选物。 一些方法包括鉴定用FOXP3调节FOXP1的异源寡聚化的化学候选物和/或其包含Z-LeuZip结构域的片段。 一些方法包括鉴定调节IL-2启动子与FOXP3和/或其包含Zinc-LeuZip结构域的片段的相互作用的化学候选物。 治疗患有或怀疑患有自身免疫性疾病,炎症性疾病,细胞,组织或器官移植或冠状动脉疾病的个体的方法,以及治疗患有或怀疑患有感染性疾病,癌症或免疫受损的个体的方法 或接受疫苗接种。

    FAS PEPTIDE MIMETICS AND USES THEREOF
    8.
    发明申请
    FAS PEPTIDE MIMETICS AND USES THEREOF 有权
    FAS PEPTIDE MIME及其用途

    公开(公告)号:US20120245081A1

    公开(公告)日:2012-09-27

    申请号:US13210117

    申请日:2011-08-15

    CPC classification number: C07K14/70578 A61K38/00

    Abstract: Exocyclic peptide mimetics that disable Fas were developed. A three dimensional model of the Fas receptor-ligand complex was constructed and structurally predicted regions of the receptor that were relevant to binding ligand were used to create constrained peptide mimetics. Exocyclic anti-Fas peptide mimetics were identified that block Fas receptor-ligand interactions, and modulate Fas biological activity both in vitro and in vivo. The mimetics are useful, e.g., for treating Fas-related pathologies.

    Abstract translation: 开发了禁用Fas的外来肽模拟物。 构建了Fas受体 - 配体复合物的三维模型,并且结构上预测与结合配体相关的受体区域用于产生约束肽模拟物。 鉴定了外环抗Fas肽模拟物阻断Fas受体 - 配体相互作用,并在体外和体内调节Fas生物活性。 模拟物可用于例如治疗Fas相关病理学。

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