Patents by Inventor Kazumasa Ogasawara

Kazumasa Ogasawara 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).

  • Publication number: 20230174586
    Abstract: Provided are: a recombinant vaccinia virus which is effective for the prevention of the development of a disease by the infection by H7 avian influenza virus and has high safety; and a vaccine against H7 avian influenza virus, which comprises the recombinant vaccinia virus. The recombinant vaccinia virus according to the present invention is a recombinant vaccinia virus having such a structure that an expression promoter and the full length or a part of cDNA encoding hemagglutinin protein of H7 avian influenza virus are contained in the genome for vaccinia virus strain DIs.
    Type: Application
    Filed: November 14, 2019
    Publication date: June 8, 2023
    Applicants: TOKYO METROPOLITAN INSTITUTE OF MEDICAL SCIENCE, SHIGA UNIVERSITY OF MEDICAL SCIENCE
    Inventors: Fumihiko YASUI, Michinori KOHARA, Kenzaburo YAMAJI, Yasushi ITOH, Kazumasa OGASAWARA, Koji ISHII
  • Patent number: 11633716
    Abstract: An objective of the present disclosure is to provide an adsorption material that has a carrier material with retained physical strength, and efficiently adsorbs an immunosuppressive protein. The present disclosure provides an adsorption material for immunosuppressive protein. The adsorption material includes a water-insoluble carrier to which at least one nitrogen-containing compound selected from a polyamine represented by a predetermined formula and aliphatic amines represented by predetermined formulae is bound. A total content of amino groups on the water-insoluble carrier is more than 0 ?mol and 2500 ?mol or less per 1 g, and a content of primary amino groups on the water-insoluble carrier is 450 ?mol or less per 1 g.
    Type: Grant
    Filed: September 7, 2018
    Date of Patent: April 25, 2023
    Assignees: TORAY INDUSTRIES, INC., NATIONAL UNIVERSITY CORPORATION SHIGA UNIVERSITY OF MEDICAL SCIENCE
    Inventors: Junichi Kasuya, Ryo Matsunaga, Yoshiyuki Ueno, Yuji Ueda, Kazuo Teramoto, Kazumasa Ogasawara
  • Publication number: 20200246776
    Abstract: An objective of the present disclosure is to provide an adsorption material that has a carrier material with retained physical strength, and efficiently adsorbs an immunosuppressive protein. The present disclosure provides an adsorption material for immunosuppressive protein. The adsorption material includes a water-insoluble carrier to which at least one nitrogen-containing compound selected from a polyamine represented by a predetermined formula and aliphatic amines represented by predetermined formulae is bound. A total content of amino groups on the water-insoluble carrier is more than 0 ?mol and 2500 ?mol or less per 1 g, and a content of primary amino groups on the water-insoluble carrier is 450 ?mol or less per 1 g.
    Type: Application
    Filed: September 7, 2018
    Publication date: August 6, 2020
    Applicants: TORAY INDUSTRIES, INC., NATIONAL UNIVERSITY CORPORATION SHIGA UNIVERSITY OF MEDICAL SCIENCE
    Inventors: Junichi KASUYA, Ryo MATSUNAGA, Yoshiyuki UENO, Yuji UEDA, Kazuo TERAMOTO, Kazumasa OGASAWARA
  • Publication number: 20200215253
    Abstract: An objective of the present disclosure is to provide an adsorption material that can selectively adsorb immunosuppressive leukocyte. The present disclosure provides an adsorption material for immunosuppressive leukocyte. The adsorption material includes a water-insoluble carrier to which at least one nitrogen-containing compound selected from a polyamine represented by a predetermined formula and aliphatic amines represented by predetermined formulae are bound. A form of the water-insoluble carrier is a fiber or a particle, a diameter of the fiber or the particle is 15 to 50 ?m, and an arithmetic mean roughness of a surface of the water-insoluble carrier is 0.1 to 3.0 ?m.
    Type: Application
    Filed: September 7, 2018
    Publication date: July 9, 2020
    Applicants: TORAY INDUSTRIES, INC., NATIONAL UNIVERSITY CORPORATION SHIGA UNIVERSITY OF MEDICAL SCIENCE
    Inventors: Yoshiyuki UENO, Junichi KASUYA, Toru ARAKANE, Ryo MATSUNAGA, Yumiko SEKIYA, Yuji UEDA, Kazuo TERAMOTO, Kazumasa OGASAWARA
  • Patent number: 9127250
    Abstract: This invention discloses an immunosuppressive cell-capturing material comprising a molded body that includes: a readily hydrolyzable condensation polymer having an amino group; a poorly hydrolyzable polymer coating the readily hydrolyzable condensation polymer; and a ligand-conjugated poorly hydrolyzable polymer coating the poorly hydrolyzable polymer, wherein the ligand is at least one selected from the group consisting of a NH2 group, a secondary amino group, a tertiary amino group, a polyamine residue, a basic cyclic polypeptide residue, an aminoglycosidic compound residue, chloroquine, primaquine, mefloquine, imiquimod, and nystatin, and wherein the content of the amino group in the molded body is 150 ?mol/g or less. The invention also discloses an immunosuppressive cell-capturing column filled with the capturing material.
    Type: Grant
    Filed: March 27, 2012
    Date of Patent: September 8, 2015
    Assignee: Shiga University of Medical Science
    Inventors: Kazumasa Ogasawara, Kazuo Teramoto, Yuji Ueda, Yasushi Itoh, Hirohito Ishigaki
  • Publication number: 20140017667
    Abstract: This invention discloses an immunosuppressive cell-capturing material comprising a molded body that includes: a readily hydrolyzable condensation polymer having an amino group; a poorly hydrolyzable polymer coating the readily hydrolyzable condensation polymer; and a ligand-conjugated poorly hydrolyzable polymer coating the poorly hydrolyzable polymer, wherein the ligand is at least one selected from the group consisting of a NH2 group, a secondary amino group, a tertiary amino group, a polyamine residue, a basic cyclic polypeptide residue, an aminoglycosidic compound residue, chloroquine, primaquine, mefloquine, imiquimod, and nystatin, and wherein the content of the amino group in the molded body is 150 ?mol/g or less. The invention also discloses an immunosuppressive cell-capturing column filled with the capturing material.
    Type: Application
    Filed: March 27, 2012
    Publication date: January 16, 2014
    Applicant: SHIGA UNIVERSITY OF MEDICAL SCIENCE
    Inventors: Kazumasa Ogasawara, Kazuo Teramoto, Yuji Ueda, Yasushi Itoh, Hirohito Ishigaki
  • Publication number: 20080044391
    Abstract: It is intended to provide expired dendritic cells having characteristics of the following (E1) to (E3): (E1) not shifting into a mature type due to an action of a natural immune stimulant or a permanent immune potentiator; (E2) having the same shape as immature DC; and (E3) expressing IL-10. It is intended to provide Permanently activated dendritic cells having the following characteristics: (M2-1) having projecting dendrites and forming aggregation clusters; (M2-2) being capable of activating unreacted cytotoxic T cells (CTL); (M2-3) having stable properties under the action of anti-CD40 monoclonal antibody; and (M2-4) showing a high expression level of at least one member selected from the group consisting of CD80, CD83 and CD86.
    Type: Application
    Filed: March 9, 2006
    Publication date: February 21, 2008
    Applicant: KANSAI TECHNOLOGY LICENSING ORGANIZATION CO., LTD.
    Inventors: Kazumasa Ogasawara, Kiichi Kajino, Ichiro Nakamura, Keiichi Kontani
  • Publication number: 20060147434
    Abstract: It is intended to provide expired dendritic cells having characteristics of the following (E1) to (E3): (E1) not shifting into a mature type due to an action of a natural immune stimulant or a permanent immune potentiator;(E2) having the same shape as immature DC; and (E3) expressing IL-10. It is intended to provide Permanently activated dendritic cells having the following characteristics:(M2-1) having projecting dendrites and forming aggregation clusters;(M2-2) being capable of activating unreacted cytotoxic T cells (CTL);(M2-3) having stable properties under the action of anti-CD40 monoclonal antibody; and (M2-4) showing a high expression level of at least one member selected from the group consisting of CD80, CD83 and CD86.
    Type: Application
    Filed: January 16, 2004
    Publication date: July 6, 2006
    Inventors: Kazumasa Ogasawara, Kaiichi Kajino, Ichiro Nakamura, Keiichi Kontani