Immunomodulator
    2.
    发明申请
    Immunomodulator 审中-公开

    公开(公告)号:US20060252700A1

    公开(公告)日:2006-11-09

    申请号:US11484605

    申请日:2006-07-12

    摘要: An immunomodulator is provided which is capable of oral intake for improvement, treatment and prevention of human immunological diseases and which is used to treat, improve and prevent human immunological diseases, especially, autoimmune diseases and allergic diseases such as hepatic cirrhosis, hepatitis, diabetes, inflammatory bowel diseases, chronic rheumatoid arthritis, asthma and cutaneous atopy, allergic diseases and cancers by a new method that can control the redox state of macrophages or monocytes, and can be incorporated into a drug, a food, a nutrient, and an infusion. The contents of oxidative glutathione and reductive glutathione in macrophages are monitored, and the ratio of oxidative glutathione and reductive glutathione is examined, whereby macrophages are classified into oxidative macrophages and reductive macrophages having different functions. The degree of progression of various autoimmune diseases is analyzed from this standpoint. On the basis of the results, an immunomodulator capable of oral intake which contains a substance having an activity of changing a content of reductive glutathione in macrophages to solve the above-mentioned problem and which is intended to treat, improve and prevent human immune diseases is provided.

    .gamma.-chain humaninterleukin-2 receptor polypeptide and method of
making
    4.
    发明授权
    .gamma.-chain humaninterleukin-2 receptor polypeptide and method of making 失效
    γ链人类白细胞介素-2受体多肽及其制备方法

    公开(公告)号:US5856140A

    公开(公告)日:1999-01-05

    申请号:US636936

    申请日:1996-04-24

    摘要: A polypeptide which specifically binds to the .gamma.-chain of the human interleukin-2 receptor and selectively inhibits the binding of the .gamma.-chain of human interleukin-2 receptor to the .beta.-chain of the same is provided. The polypeptide has an activity of blocking the human interleukin-2 response. Also provided are an immunosuppressant containing the polypeptide, a DNA gene coding for the polypeptide, a recombinant DNA having the gene, a transformant having the recombinant DNA, and a method for producing the intended polypeptide by incubating the transformant. The novel polypeptide can be used independently, or with substances capable of inhibiting the binding of interleukin-2 to the interleukin-2 receptor, as a medicine for preventing the rejection of grafts after transplantation and also for curing inflammatory diseases such as allergic diseases and autoimmune diseases.

    摘要翻译: 提供了特异性结合人白细胞介素-2受体的γ-链的多肽,并选择性地抑制人白细胞介素-2受体的γ-链与β-链的结合。 该多肽具有阻断人白介素-2应答的活性。 还提供了含有多肽的免疫抑制剂,编码该多肽的DNA基因,具有该基因的重组DNA,具有该重组DNA的转化体,以及通过温育该转化体来制备该多肽的方法。 该新型多肽可以独立使用,也可以与能够抑制白介素-2与白细胞介素-2受体结合的物质用作防止移植后移植物排斥的药物,还可用于治疗炎性疾病如过敏性疾病和自身免疫性 疾病

    Method and reagent detecting human disorders
    5.
    发明授权
    Method and reagent detecting human disorders 失效
    用于检测人类疾病的方法和试剂

    公开(公告)号:US5801003A

    公开(公告)日:1998-09-01

    申请号:US568427

    申请日:1995-12-06

    CPC分类号: C07K16/2866 G01N33/6869

    摘要: The invention provides a method for detecting (1) leukemia, (2) cancer, (3) autoimmune disorder, (4) inflammatory disorder, (5) allergic disorder or (6) viral infection, characterized by measuring soluble, human interleukin-2 receptor .gamma.-chain molecules existing in a human body fluid by an immunochemical method using an antibody/antibodies specifically reacting with human interleukin-2 receptor .gamma.-chain molecule, and a reagent for the detection.

    摘要翻译: 本发明提供一种检测白血病,(2)癌症,(3)自身免疫性疾病,(4)炎症性疾病,(5)过敏性疾病或(6)病毒感染的方法,其特征在于测量可溶性人白介素-2 通过使用与人白细胞介素-2受体γ链分子特异性反应的抗体/抗体的免疫化学方法和用于检测的试剂,存在于人体液中的受体γ链分子。

    Ligand for the neu gene product
    8.
    发明授权
    Ligand for the neu gene product 失效
    配体为neu基因产物

    公开(公告)号:US5464751A

    公开(公告)日:1995-11-07

    申请号:US927422

    申请日:1992-09-24

    摘要: A purified proteinaceous substance bindable with p185, the translation product of the neu oncogene is disclosed. The purified proteinaceous substance may be characterized in that it increases the activity of the tyrosine kinase contained in the neu oncogene product but does not increase the activity of tyrosine kinase of epidermal growth factor receptor; induces p185 dimerization and internalization; affects the growth of cells which express p185 in a dose dependent manner; is heat stable from about 56.degree. C. to about 100.degree. C.; is degradable by protease; and has a molecular weight of from about 7,000 to about 14,000 daltons in its smallest active form as determined by gel filtration and ultrafiltration membrane analysis. Methods of detecting p185 on the surfaces of tumor cells are also disclosed.

    摘要翻译: PCT No.PCT / US91 / 02331 Sec。 371日期:1992年9月24日 102(e)日期1992年9月24日PCT 1991年4月4日PCT PCT。 出版物WO91 / 15230 PCT 日期为1991年10月17日。公开了一种与p185结合的纯化蛋白质物质,即neu致癌基因的翻译产物。 纯化的蛋白质物质的特征在于其增加neu致癌基因产物中所含的酪氨酸激酶的活性,但不增加表皮生长因子受体酪氨酸激酶的活性; 诱导p185二聚化和内化; 以剂量依赖的方式影响表达p185的细胞的生长; 从约56℃至约100℃是热稳定的。 可通过蛋白酶降解; 并且通过凝胶过滤和超滤膜分析测定,其最小活性形式的分子量为约7,000至约14,000道尔顿。 还公开了在肿瘤细胞表面检测p185的方法。