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    • 4. 发明申请
    • SYNERGISTIC COMPOSITIONS OF SOLUBLE COMPLEMENT RECEPTORS AND COMPOUNDS THAT INHIBIT COMPLEMENT AND/OR SUPPRESS IMMUNE ACTIVITY
    • 可溶性补体受体的协同组合物和禁止补充和/或抑制免疫活性的化合物
    • WO1992010205A1
    • 1992-06-25
    • PCT/US1991009300
    • 1991-12-06
    • T CELL SCIENCES, INC.MARSH, Henry, C., Jr.KUNG, Patrick, C.
    • T CELL SCIENCES, INC.
    • A61K37/48
    • C07K14/705A61K31/343A61K31/41A61K38/166A61K38/1709A61K38/177A61K38/482A61K38/49A61K45/06A61K2300/00
    • The present invention relates to synergistic therapeutic compositions of synergistic combinations of organic and biological compounds which inhibit complement and/or possess immunosuppressive activity, and the therapeutic uses thereof. The organic compounds of the invention are compounds which exhibit immunosuppressive and/or anti-inflammatory activity. Such organic compounds include but are not limited to K-76, K-76 COOH and derivatives and synthetic analogs thereof, antimetabolites, antimitotic drugs, cyclosporine, steroids, and non-steroidal anti-inflammatory agents. In a particular aspect, the organic compounds of the invention include substituted dihydrobenzofurans, substituted and unsubstituted spirobenzofuran-2(3H)-cycloalkanes, and their open chain intermediates which exhibit such inhibitory ativities. The biological compounds of the invention are complement receptors or fragments thereof and soluble members of the complement receptor family that contain the conserved SCR motif and that are able to inhibit complement activity. The biological compounds exhibit at least one of the functions associated with complement receptors and/or SCR containing proteins. The invention relates to the use of mixtures of these compounds for therapy of immune and/or inflammatory disorders.
    • 本发明涉及抑制补体和/或具有免疫抑制活性的有机和生物化合物的协同组合的协同治疗组合物及其治疗用途。 本发明的有机化合物是具有免疫抑制和/或抗炎活性的化合物。 这些有机化合物包括但不限于K-76,K-76 COOH及其衍生物和合成类似物,抗代谢物,抗有丝分裂药物,环孢霉素,类固醇和非甾体抗炎剂。 在一个具体方面,本发明的有机化合物包括取代的二氢苯并呋喃,取代和未取代的螺苯并呋喃-2(3H) - 环烷烃及其开链中间体,其表现出这种抑制活性。 本发明的生物化合物是补体受体或其片段和补体受体家族的可溶性成员,其含有保守的SCR基序并能够抑制补体活性。 生物化合物显示与补体受体和/或含SCR蛋白相关的功能中的至少一个。 本发明涉及这些化合物的混合物用于治疗免疫和/或炎性疾病的用途。
    • 6. 发明申请
    • DIAGNOSIS AND THERAPY OF SARCOIDOSIS
    • 诊断和治疗SARCOIDOSIS
    • WO1994014067A1
    • 1994-06-23
    • PCT/US1992010779
    • 1992-12-14
    • T CELL SCIENCES, INC.WIGZELL, HansGRÜNEWALD, JohannJONSON, Carl-HaraldJONES, Nancy
    • T CELL SCIENCES, INC.
    • G01N33/53
    • C07K14/7051A61K38/00C07K16/2809C12Q1/6883C12Q2600/156C12Q2600/158C12Q2600/172G01N33/56972G01N2800/52
    • Sarcoidosis is associated with CD4 T lymphocytes which express the T cell receptor V alpha 2.3 chain. Thus, a method for diagnosing sarcoidosis is provided which comprises contacting cells of a subject with a first monoclonal antibody, or an antigen-binding fragment or derivative, specific for an epitope of the variable region of the T cell receptor V alpha 2.3 chain and detecting the binding of the antibody. Also provided is a method for treating sarcoidosis in which a monoclonal antibody, or an antigen-binding fragment or derivative thereof, specific for an epitope of the variable region of the T cell receptor V alpha 2.3 chain is administered. Sarcoidosis is also treated by administering a therapeutically effective amount of a protein or a peptide comprising an amino acid sequence of the variable region of the T cell receptor V alpha 2.3 chain, or a functional derivative of the protein or peptide, or an antisense oligonucleotide which is complementary to the T cell receptor V alpha 2.3 mRNA.
    • 结节病与表达T细胞受体Vα2链的CD4 + T淋巴细胞有关。 因此,提供了一种用于诊断结节病的方法,其包括使受试者的细胞与特异于T细胞受体Vα2链的可变区的表位的第一单克隆抗体或抗原结合片段或衍生物接触并检测 抗体的结合。 还提供了治疗结节病的方法,其中施用特异于T细胞受体Vα2链的可变区的表位的单克隆抗体或其抗原结合片段或衍生物。 还可以通过施用治疗有效量的蛋白质或包含T细胞受体Vα2链的可变区的氨基酸序列或蛋白质或肽的功能性衍生物的肽或反义寡核苷酸来治疗结节病, 与T细胞受体Vα2.3mRNA互补。