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    • 71. 发明申请
    • POLYNUCLEOTIDE THERAPY
    • 多核苷酸治疗
    • US20090264515A1
    • 2009-10-22
    • US12467866
    • 2009-05-18
    • Paulo FontouraHideki GarrenWilliam H. RobinsonLawrence SteinmanPedro Jose RuizPaul J. Utz
    • Paulo FontouraHideki GarrenWilliam H. RobinsonLawrence SteinmanPedro Jose RuizPaul J. Utz
    • A61K31/7088A61P21/00
    • A61K39/001A61K38/2026A61K39/0007A61K39/0008A61K48/00A61K2039/53A61K2039/55522A61K2039/55561C07K2319/30
    • This invention provides a method of treating or preventing a disease in an animal associated with one or more self-protein(s), -polypeptide(s), or -peptide(s) that is present or involved in a non-physiologic process in the animal comprising administering to the animal a self-vector comprising a polynucleotide encoding the self-protein(s), -polypeptide(s) or -peptide(s) associated with the disease. Administration of the self-vector comprising a polynucleotide encoding the self-protein(s), -polypeptide(s) or -peptide(s) modulates an immune response to the self-protein(s), -polypeptide(s) or -peptide(s) expressed from administration of the self-vector. The invention also provides a composition comprising a polynucleotide encoding one or more self-protein(s), -polypeptide(s), or -peptide(s) that is present non-physiologically in a treated animal useful in treating or preventing a disease associated with the self-protein(s), -polypeptide(s), or -peptide(s) present in and/or the target of a non-physiologic process in the animal.
    • 本发明提供了一种治疗或预​​防与一种或多种自身蛋白,多肽或肽存在或参与非生理过程的一种或多种自身相关的动物疾病的方法, 所述动物包括向所述动物施用包含编码与所述疾病相关的自身蛋白质多肽或多肽的多核苷酸的自身载体。 施用包含编码自身蛋白,多肽或多肽的多核苷酸的自身载体调节对自身蛋白质的多肽或肽的免疫应答 (s)表示自我向量的管理。 本发明还提供了一种组合物,其包含编码一种或多种自身蛋白质,多肽或多肽或多肽的多核苷酸,所述多肽或多肽在治疗动物中非生理性地存在,可用于治疗或预防相关疾病 其中存在于动物的非生理过程的和/或靶中的自身蛋白质,多肽或多肽。
    • 74. 发明授权
    • Methods of inducing T-cell non-responsiveness with anti-gp39 24-31 antibodies
    • 用抗gp39 24-31抗体诱导T细胞非反应性的方法
    • US07501124B2
    • 2009-03-10
    • US10962033
    • 2004-10-07
    • Randolph J. NoelleFiona H. DurieDavid C. ParkerMichael C. AppelNancy E. PhillipsJohn P. MordesDale L. GrenierAldo A. Rossini
    • Randolph J. NoelleFiona H. DurieDavid C. ParkerMichael C. AppelNancy E. PhillipsJohn P. MordesDale L. GrenierAldo A. Rossini
    • A61K39/395A61K35/26A61K35/28C07K16/28
    • A61K39/001A61K35/17A61K35/39A61K38/00A61K2039/505C07K14/705C07K16/2875C07K2317/73Y10S514/885A61K2300/00
    • Methods for inducing T cell tolerance to a tissue or organ graft in a transplant recipeint are disclosed. The methods involve administering to a subject: 1) an allogeneic or xenogeneic cell which expresses donor antigens and which has a ligand on the cell surface which interacts with a receptor on the surface of a recipient T cell which mediates contact-dependent helper effector function; and 2) an antagonist of the receptor which inhibits interaction of the ligand with the receptor. In a preferred embodiment, the allogeneic or xenogeneic cell is a B cell, preferably a resting B cell, and the molecule on the surface of the T cell which mediates contact-dependent helper effector function is gp39. A preferred gp39 antagonist is an anti-gp39 antibody. The allogeneic or xenogeneic cell and the gp39 antagonist are typically administered to a transplant recipient prior to transplantation of the tissue or organ. The methods of the invention can be used to induce T cell tolerance to transplants such as liver, kidney, heart, lung, skin, muscle, neuronal tissue, stomach and intestine. A method for treating diabetes comprising administering to a subject allogeneic or xenogeneic cells expressing donor antigens, a gp39 antagonist and pancreatic islets is also disclosed.
    • 公开了在移植食谱中诱导T细胞对组织或器官移植物的耐受性的方法。 所述方法包括对受试者施用:1)同种异体或异种细胞,其表达供体抗原,并且其在细胞表面上具有与介导接触依赖性辅助效应子功能的受体T细胞表面上的受体相互作用的配体; 和2)抑制配体与受体相互作用的受体拮抗剂。 在一个优选的实施方案中,同种异体或异种细胞是B细胞,优选静止的B细胞,并且介导接触依赖性辅助效应子功能的T细胞表面上的分子是gp39。 优选的gp39拮抗剂是抗gp39抗体。 同种异体或异种细胞和gp39拮抗剂通常在移植组织或器官之前给予移植受体。 本发明的方法可用于诱导移植物如肝,肾,心脏,肺,皮肤,肌肉,神经元组织,胃和肠的T细胞耐受性。 还公开了一种用于治疗糖尿病的方法,其包括向受试者施用表达供体抗原的同种异体或异种细胞,gp39拮抗剂和胰岛。