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    • 6. 发明申请
    • REDIRECTED, GENETICALLY-ENGINEERED T REGULATORY CELLS AND THEIR USE IN SUPPRESSION OF AUTOIMMUNE AND INFLAMMATORY DISEASE
    • 重定向,遗传工程化的T细胞及其在抑制自身免疫和炎症疾病中的应用
    • US20100135974A1
    • 2010-06-03
    • US12525270
    • 2008-01-31
    • Zelig EshharEran Elinav
    • Zelig EshharEran Elinav
    • A61K35/12C12N5/10C07H21/04C07K16/00A61P29/00A61P37/00
    • C12N5/0636A61K39/0008A61K39/0011
    • A redirected Treg cell is endowed with specificity toward a selected target antigen or ligand. The cell contains a chimeric receptor polypeptide that is expressed in a single, continuous chain, with an extracellular recognition region displayed on the surface of the cell, a transmembrane region and an intracellular signaling region. The extracellular recognition region is specific for the selected target antigen or ligand. The intracellular signaling region includes a combination of T-cell signaling polypeptide moieties, which combination, upon binding of the extracellular recognition region to the selected target antigen or ligand, triggers activation of the redirected Treg cells to cause suppression of T-cell mediated immunity. Such redirected Treg cells may be used to suppress undesired activity of T effector cells thereby mediating an immune or inflammatory response. They are particularly useful in treating T effector cell-mediated diseases, such as inflammatory bowel disease, transplant rejection and GVH disease.
    • 重定向的Treg细胞被赋予对所选靶抗原或配体的特异性。 细胞含有在单个连续链中表达的嵌合受体多肽,细胞外识别区域显示在细胞表面,跨膜区和胞内信号传导区。 细胞外识别区域对于所选择的靶抗原或配体是特异性的。 细胞内信号传导区域包括T细胞信号传导多肽部分的组合,当细胞外识别区域与所选择的靶抗原或配体结合时,其组合触发重定向的Treg细胞的激活以引起T细胞介导的免疫的抑制。 这种重定向的Treg细胞可以用于抑制T效应细胞的不期望的活性,从而介导免疫或炎症反应。 它们特别可用于治疗T效应细胞介导的疾病,例如炎症性肠病,移植排斥和GVH疾病。
    • 7. 发明授权
    • Detection of small molecules by use of a piezoelectric sensor
    • 通过使用压电传感器检测小分子
    • US07135295B1
    • 2006-11-14
    • US09889936
    • 2000-01-25
    • Itamar WillnerZelig Eshhar
    • Itamar WillnerZelig Eshhar
    • G01N33/53
    • C07K16/00G01N33/54373
    • A protein comprising an antigen-binding portion formed by two cooperating peptide sequences of FIGS. 3A and 3B of the application. The protein may alternatively comprise an altered antigen-binding portion where at least one of the peptide sequences is an altered sequence, an altered sequence being a sequence of FIG. 3A or 3B in which one or more of an amino acid residue has been added, deleted or replaced by another amino acid residue. The altered antigen-binding portion retains substantially the same antigen-binding specificity as said antigen-binding portion. Also disclosed are apparatus, systems and methods for detecting small assayed molecules in a sample using the protein.
    • 包含由图1和2的两个协同肽序列形成的抗原结合部分的蛋白质。 3 A和3 B的应用程序。 蛋白质可以可选地包含改变的抗原结合部分,其中至少一个肽序列是改变的序列,改变的序列是图1的序列。 3 A或3 B,其中一个或多个氨基酸残基已经被另一个氨基酸残基加入,缺失或替换。 改变的抗原结合部分保持与所述抗原结合部分基本相同的抗原结合特异性。 还公开了用于使用蛋白质检测样品中的小测定分子的装置,系统和方法。
    • 8. 发明授权
    • Endowing lymphocytes with antibody specificity
    • 赋予淋巴细胞抗体特异性
    • US5906936A
    • 1999-05-25
    • US55396
    • 1993-05-04
    • Zelig EshharGideon GrossTova Waks
    • Zelig EshharGideon GrossTova Waks
    • C07K14/725C07K16/44C12N15/13C07H21/04C07K16/46
    • C07K14/7051C07K16/44C07K2317/56C07K2319/00C07K2319/02
    • There are produced recombinant gene pairs which endow mononuclear cells, mainly various lymphocyte type cells, with antibody-type specificity. In specific gene pairs the rearranged gene pairs code for a binding site of an antibody molecule from the same species, of the T-cell receptor gene, or another species. Gene pairs of the invention code, for example, for antibodies specific towards tumor-specific antigens, viral antigens, modified self antigens, bacterial or fungal antigens, autoimmune type disease antigens and the like. The invention further relates to expression vectors for the effective transfection of such cell types comprising such a recombinant gene pair, to methods for producing same and to pharmaceutical compositions comprising as active ingredient an effective quantity of lymphocytes transfected with such gene pairs.
    • 产生了具有抗体型特异性的单核细胞,主要是各种淋巴细胞型细胞的重组基因对。 在特定基因对中,重排的基因对编码来自相同物种,T细胞受体基因或其他物种的抗体分子的结合位点。 本发明的基因对编码例如针对肿瘤特异性抗原特异性抗体,病毒抗原,修饰的自身抗原,细菌或真菌抗原,自身免疫型疾病抗原等。 本发明进一步涉及用于有效转染包含这种重组基因对的这种细胞类型的表达载体,其生产方法和包含作为活性成分的有效量的用这种基因对转染的淋巴细胞的药物组合物。