Patents by Inventor Akihiro KOUBE

Akihiro KOUBE 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: 11472867
    Abstract: An anti-HSV monoclonal antibody or an antigen-binding fragment thereof is an anti-HSV gB monoclonal antibody or an antigen-binding fragment thereof that specifically binds to herpes simplex virus (HSV) envelope glycoprotein B (gB), comprising: a heavy chain variable region comprising a heavy chain CDR1 consisting of the amino acid sequence set forth in SEQ ID NO: 3, a heavy chain CDR2 consisting of the amino acid sequence set forth in SEQ ID NO: 4, and a heavy chain CDR3 consisting of the amino acid sequence set forth in SEQ ID NO: 5; and a light chain variable region comprising a light chain CDR1 consisting of the amino acid sequence set forth in SEQ ID NO: 6, a light chain CDR2 consisting of the amino acid sequence set forth in SEQ ID NO: 7, and a light chain CDR3 consisting of the amino acid sequence set forth in SEQ ID NO: 8.
    Type: Grant
    Filed: August 29, 2018
    Date of Patent: October 18, 2022
    Assignee: KM BIOLOGICS CO., LTD.
    Inventors: Hiroaki Mori, Tomohiro Nishimura, Hiroyuki Shimizu, Akihiro Koube
  • Patent number: 11357847
    Abstract: The modified HSV gD protein of the present invention is a modified protein of a herpes simplex virus (HSV) envelope glycoprotein D (gD), wherein the modified HSV gD protein is derived from a wild-type HSV gD by modification of at least one of B cell epitopes having low or no neutralizing antibody-inducing activity compared to a B cell epitope present in a receptor-binding domain (RBD) (decotopes) in the ectodomain of the wild-type HSV gD, so that the modified epitope does not function as an epitope.
    Type: Grant
    Filed: August 29, 2018
    Date of Patent: June 14, 2022
    Assignee: KM BIOLOGICS CO., LTD.
    Inventors: Hiroaki Mori, Tomohiro Nishimura, Hiroyuki Shimizu, Akihiro Koube, Takahiro Katayama
  • Publication number: 20210346494
    Abstract: The present invention is directed to provide a modified CMV gB protein that can induce a group of antibodies including a high ratio of neutralizing antibodies that exhibit a high neutralizing activity against a CMV gB protein, in comparison with a wild type CMV gB, upon induction of immunity and that can be used in the prevention and/or treatment of CMV infection and a CMV vaccine comprising the modified CMV gB protein. The modified CMV gB protein according to the present invention is a modified CMV gB protein having an improved ability to induce body region-recognizing antibodies and comprising modification in a head region.
    Type: Application
    Filed: October 24, 2019
    Publication date: November 11, 2021
    Inventors: Masaharu TORIKAI, Hiroaki MORI, Tomohiro NISHIMURA, Miyuki MATSUMOTO, Hiroyuki SHIMIZU, Akihiro KOUBE, Takamasa NAGATOMO, Naoki INOUE
  • Publication number: 20210205441
    Abstract: The modified HSV gD protein of the present invention is a modified protein of a herpes simplex virus (HSV) envelope glycoprotein D (gD), wherein the modified HSV gD protein is derived from a wild-type HSV gD by modification of at least one of B cell epitopes having low or no neutralizing antibody-inducing activity compared to a B cell epitope present in a receptor-binding domain (RBD) (decotopes) in the ectodomain of the wild-type HSV gD, so that the modified epitope does not function as an epitope.
    Type: Application
    Filed: August 29, 2018
    Publication date: July 8, 2021
    Inventors: Hiroaki MORI, Tomohiro NISHIMURA, Hiroyuki SHIMIZU, Akihiro KOUBE, Takahiro KATAYAMA
  • Publication number: 20200239549
    Abstract: An anti-HSV monoclonal antibody or an antigen-binding fragment thereof is an anti-HSV gB monoclonal antibody or an antigen-binding fragment thereof that specifically binds to herpes simplex virus (HSV) envelope glycoprotein B (gB), comprising: a heavy chain variable region comprising a heavy chain CDR1 consisting of the amino acid sequence set forth in SEQ ID NO: 3, a heavy chain CDR2 consisting of the amino acid sequence set forth in SEQ ID NO: 4, and a heavy chain CDR3 consisting of the amino acid sequence set forth in SEQ ID NO: 5; and a light chain variable region comprising a light chain CDR1 consisting of the amino acid sequence set forth in SEQ ID NO: 6, a light chain CDR2 consisting of the amino acid sequence set forth in SEQ ID NO: 7, and a light chain CDR3 consisting of the amino acid sequence set forth in SEQ ID NO: 8.
    Type: Application
    Filed: August 29, 2018
    Publication date: July 30, 2020
    Inventors: Hiroaki MORI, Tomohiro NISHIMURA, Hiroyuki SHIMIZU, Akihiro KOUBE