Patents by Inventor Yasuhiko Masuho

Yasuhiko Masuho has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).

  • Patent number: 5506111
    Abstract: A method of immunologically assaying intact human osteocalcin in a human assay sample is provided by using an antibody having an epitope in a region of an amino acid sequence 1 to 20 on the N-terminal side of human osteocalcin and an antibody having an epitope in a region of an amino acid sequence 36 to 49 on the C-terminal side of human osteocalcin. A reagent and a kit therefor are provided. Furthermore, a method of immunologically assaying the total amount of human intact osteocalcin in a human assay sample, and a reagent and a kit therefor are also provided. A monoclonal antibody and a polyclonal antibody are used for the assay. A process for producing these antibodies, and utilization of these antibodies is described.
    Type: Grant
    Filed: October 3, 1994
    Date of Patent: April 9, 1996
    Assignee: Teijin Limited
    Inventors: Kenji Hosoda, Hitomi Honda, Takaharu Kubota, Yasuhiko Masuho
  • Patent number: 5445960
    Abstract: Human IgG1 monoclonal antibodies are produced by hybridoma ATCC HB10074 and bind to gp120 of HIV.
    Type: Grant
    Filed: May 24, 1993
    Date of Patent: August 29, 1995
    Assignees: The Arizona Board of Regents on behalf of the University of Arizona, Teijin Limited
    Inventors: Yasuhiko Masuho, Toru Sugano, Yoh-Ichi Matsumoto, Evan M. Hersh, Eskild A. Petersen, Douglas Lake, Takashi Kawamura
  • Patent number: 5298393
    Abstract: A monoclonal antibody for human acid glutathion S-transferase. This monoclonal antibody can be utilized as a diagnostic for cancers such as cancer of liver, gastric cancer, and cancer of the blood.
    Type: Grant
    Filed: September 16, 1991
    Date of Patent: March 29, 1994
    Assignee: Teijin Limited
    Inventors: Ichiro Urushizaki, Yoshiro Niitsu, Hiroshi Maruyama, Hideaki Suzuki, Kenji Hosoda, Hitomi Honda, Yasuhiko Masuho
  • Patent number: 5298419
    Abstract: The invention is directed to the human hybridoma designated MCA 86 and having A.T.C.C. Accession No. HB 9669 and human monoclonal antibodies produced by hybridoma MCA 86. Human monoclonal antibodies produced by hybridoma MCA 86 immunologically binds to both gp41 and gp120 envelope glycoproteins of Human Immunodeficiency Virus (HIV). These monoclonal antibodies are useful in the diagnosis of HIV infection.
    Type: Grant
    Filed: March 31, 1988
    Date of Patent: March 29, 1994
    Assignees: The Arizona Board of Regents on behalf of the University of Arizona, Teijin Limited
    Inventors: Yasuhiko Masuho, Toru Sugano, Yoh-ichi Matsumoto, Evan M. Hersh, Eskild A. Peterson
  • Patent number: 5089262
    Abstract: P. aeruginosa E87Ag antigen comprising polysaccharide fraction with molecular weight of about 27,000 which is contained in lipopolysaccharide of P. aeruginosa; anti-P. aeruginosa human or mouse monoclonal antibody which recognizes said E87Ag antigen; and mouse-human or mouse-mouse hybridoma which produces said monoclonal antibody.The monoclonal antibody can be used for making diagnosis and therapy of infections with P. aeruginosa.
    Type: Grant
    Filed: June 13, 1990
    Date of Patent: February 18, 1992
    Assignee: Teijin Limited
    Inventors: Shuzo Sawada, Takashi Kawamura, Yasuhiko Masuho, Katsuhiko Tomibe
  • Patent number: 5043281
    Abstract: Human monoclonal antibodies against cytomegalovirus. These antibodies can be advantageously used as a diagnostic, or preventive and remedy for cytomegalovirus infectious diseases.
    Type: Grant
    Filed: September 27, 1990
    Date of Patent: August 27, 1991
    Assignee: Teijin Ltd.
    Inventors: Yasuhiko Masuho, Toru Sugano, Yoh-ichi Matsumoto, Shigeki Fujinaga
  • Patent number: 4950595
    Abstract: Mouse-human hybridoma, which produces monoclonal antivirus-human antibody reactive to herpes simplex virus, varicella zoster virus, and cytomegalo virus, obtained by allowing a human antibody cell, which is sensitized to virus or protein or glycoprotein arising from virus, to fuse with a mouse myeloma cell in the presence of mitogen in vitro.
    Type: Grant
    Filed: May 28, 1986
    Date of Patent: August 21, 1990
    Assignee: Teijin Limited
    Inventors: Yasuhiko Masuho, Yoh-ichi Matsumoto, Toru Sugano, Katsuhiko Tomibe
  • Patent number: 4638049
    Abstract: Antitumor protein hybrid, composed of a moiety which is substantially the fragment Fab of an antitumor immunoglobulin and a moiety which is substantially the fragment A of a diphtheria toxin, which is expressed by the following formula (I):Fab--S.sub.1 --(X).sub.n --S.sub.2 --FA).sub.m (I)(where Fab indicates a moiety which is substantially the fragment Fab of an antitumor immunoglobulin; FA indicates a moiety which is substantially the fragment A of a diphtheria toxin; X indicates a divalent organic radical; S.sub.1 and S.sub.2 are both sulfur atoms, S.sub.1 indicating a sulfur atom arising from the disulfide bond (--S--S-- bond) in an immunoglobulin and S.sub.2 a sulfur atom arising from the disulfide bond in a diphtheria toxin; n stands for 0 to 1 and m stands for an integer of 1 to 5). This antitumor protein hybrid has remarkable and specific cytotoxicity against tumor cells, e.g., in mice.
    Type: Grant
    Filed: April 4, 1980
    Date of Patent: January 20, 1987
    Assignee: Teijin Limited
    Inventors: Yasuhiko Masuho, Takeshi Hara, Teruhisa Noguchi
  • Patent number: 4450154
    Abstract: Antitumor protein hybrid, composed of a moiety which is substantially the fragment Fab of an antitumor immunogloblin and a moiety which is the subunit A of ricin, which is expressed by the following formula (I):Fab-S.sub.1 --(X).sub.n --S.sub.2 --RA).sub.m . . . (I)(where Fab indicates a moiety which is substantially the fragment Fab of an antitumor immunogloblin; RA indicates a moiety which is the subunit A of ricin; X indicates a divalent organic radical; S.sub.1 and S.sub.2 are both sulfur atoms, S.sub.1 indicating a sulfur atom arising from the disulfide bond (--S--S-- bond) in an immunoglobulin and S.sub.2 a sulfur atom arising from the disulfide bond in ricin; n stands for 0 or 1 and m stands for an integer of 1 to 5). This antitumor protein hybrid has remarkable and specific cytotoxicity against tumor cells.
    Type: Grant
    Filed: December 21, 1981
    Date of Patent: May 22, 1984
    Assignee: Teijin Limited
    Inventors: Yasuhiko Masuho, Takeshi Hara
  • Patent number: 4379145
    Abstract: Antitumor protein hybrid, having a moiety consisting of the antitumor immunoglobulin and a moiety substantially consisting of the fragment A of a diphtheria toxin, which is expressed by the following formula (I):Ab(NHCO--X--S.sub.1 --S.sub.2 --FA).sub.n (I)(where Ab indicates a moiety consisting of the antitumor immunoglobulin and FA indicates a moiety substantially consisting of the fragment A of a diphtheria toxin; X is an alkylene group or phenylene group which either has or does not have a branching of 1 to 5 carbon atoms. N in the amido bond is a nitrogen atom arising from the amino group in the antitumor immunoglobulin; S.sub.1 and S.sub.2 are both sulfur atoms, S.sub.2 indicating a sulfur atom arising from the disulfide bond in a diphtheria toxin; n stands for an integer of 1 to 5).This antitumor protein hybrid has remarkable and specific citotoxicity against tumor cells.
    Type: Grant
    Filed: December 15, 1980
    Date of Patent: April 5, 1983
    Assignees: Teijin Limited, Hidematsu Hirai
    Inventors: Yasuhiko Masuho, Naoji Umemoto, Takeshi Hara, Hidematsu Hirai
  • Patent number: 4368149
    Abstract: A protein hybrid having cytotoxicity obtained by covalently bonding an immunoglobulin or its fragment, which is capable of binding selectively to an antigen possessed by a cell to be destroyed, to a protein, which is obtained from Momordica charantia and has an activity to terminate protein synthesis. This protein hybrid displays remarkable cytotoxicity against targel cells.
    Type: Grant
    Filed: December 16, 1981
    Date of Patent: January 11, 1983
    Assignee: Teijin Limited
    Inventors: Yasuhiko Masuho, Takeshi Hara
  • Patent number: 4363758
    Abstract: A cytotoxic protein hybrid obtained by covalently bonding an immunoglobulin or its fragment, which is capable of linking selectively with an antigen possessed by a cell to be destroyed, to a protein, which is obtained from Phytolacca americana and has an activity to terminate protein synthesis. This protein hybrid displays remarkable cytotoxicity against target cells.
    Type: Grant
    Filed: December 16, 1981
    Date of Patent: December 14, 1982
    Assignee: Teijin Limited
    Inventors: Yasuhiko Masuho, Kazuo Kishida, Takeshi Hara
  • Patent number: 4357273
    Abstract: Antitumor protein hybrid, composed of a moiety which is substantially the fragment Fab of an anti-.alpha.-fetoprotein antibody and a moiety which is substantially the fragment A of a diphtheria toxin, which is expressed by the following formula (I):Fab--(S.sub.1 --(X).sub.n --S.sub.2 --FA).sub.m (I)(where Fab indicates a moiety which is substantially the fragment Fab of an anti-.alpha.-fetoprotein antibody; FA indicates a moiety which is substantially the fragment A of diphtheria toxin; X indicates a divalent organic radical; S.sub.1 and S.sub.2 are both sulfur atoms, S.sub.1 indicating a sulfur atom arising from the disulfide bond (--S--S--bond) in an anti-.alpha.-fetoprotein antibody and S.sub.2 a sulfur atom arising from the disulfide bond in a diphtheria toxin; n stands for 0 or 1 and m stands for an integer of 1 to 5). This antitumor protein hybrid has remarkable and specific citotoxicity against tumor cells.
    Type: Grant
    Filed: July 21, 1980
    Date of Patent: November 2, 1982
    Assignees: Teijin Limited, Hidematsu Hirai
    Inventors: Yasuhiko Masuho, Naoji Umemoto, Takeshi Hara, Hidematsu Hirai
  • Patent number: 4356173
    Abstract: IgM derivatives into which acyl groups expressed by the following formula (I) are introduced to make their anticomplement activity weak by acylating the free amino groups existing in IgM up to 1-90% (acylation percentage)--COR (I)where R indicates an alkyl group having 1 to 4 carbon atoms, or a carboxylated alkyl group expressed by --(CH.sub.2)mCOOH (m is 2 or 3) or --CH.dbd.CHCOOH.These IgM derivatives can be used for making immunoglobulin preparations for intravenous injection use.
    Type: Grant
    Filed: April 17, 1981
    Date of Patent: October 26, 1982
    Assignee: Teijin Limited
    Inventors: Shuzi Miura, Tsunemasa Yoshida, Shoji Ono, Yasuhiko Masuho, Shuzo Sawada
  • Patent number: 4350626
    Abstract: Antitumor protein hybrid, composed of a moiety which is substantially the fragment Fab of an antitumor immunogloblin and a moiety which is the subunit A of ricin, which is expressed by the following formula (I):Fab(S.sub.1 -(X).sub.n -S.sub.2 -RA).sub.m (I)(where Fab indicates a moiety which is substantially the fragment Fab of an antitumor immunogloblin; RA indicates a moiety which is the subunit A of ricin; X indicates a divalent organic radical; S.sub.1 and S.sub.2 are both sulfur atoms, S.sub.1 indicating a sulfur atom arising from the disulfide bond (--S--S-- bond) in an immunoglobulin and S.sub.2 a sulfur atom arising from the disulfide bond in ricin; n stands for 0 or 1 and m stands for an integer of 1 to 5). This antitumor protein hybrid has remarkable and specific cytotoxicity against tumor cells.
    Type: Grant
    Filed: July 21, 1980
    Date of Patent: September 21, 1982
    Assignee: Teijin Limited
    Inventors: Yasuhiko Masuho, Takeshi Hara
  • Patent number: 4059571
    Abstract: Novel immunoglobulin derivatives which are characterized in that in which the interchain disulfide bonds of immunoglobulin are predominantly cleaved, on the average 3 to 5 of the interchain disulfide bonds or the inter- and intra-chain disulfide bonds being cleaved, and so produced sulfur atoms (S-) are S-sulfonated (--S-SO.sub.3). The above immunoglobulin derivatives are prepared by reacting native immunoglobulin withA. a compound capable of forming tetrathionate ion, andB. a compound capable of forming in water, sulfite ion whereby cleaving on the average 3 to 5 inter-chain disulfide bonds, or inter- and intra-chain disulfide bonds, of the native immunoglobulin, and S-sulfonating (S-SO.sub.3) the so formed sulfur atoms. This invention also provides a water-soluble composition for injection containing said immunoglobulin derivative having the titre of anti-diphtheria of at least 1.0 I.U./ml at its concentration of 10.
    Type: Grant
    Filed: March 4, 1975
    Date of Patent: November 22, 1977
    Assignee: Teijin Limited
    Inventors: Katsuhiko Tomibe, Yasuhiko Masuho, Kimihiko Matsuzawa, Sachio Ishimoto, Kazuo Satake, Tsuneo Watanabe