Patents by Inventor Naozumi Harada

Naozumi Harada 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: 20230201263
    Abstract: An antigen-loaded nanogel is formed by loading or encapsulating one or more long peptide antigens or one or more protein antigens in a hydrophobized polysaccharide. The long peptide antigen(s) or protein antigen(s) contains (or each contain) one or more CD8+ cytotoxic T cell recognition epitopes and/or one or more CD4+ helper T cell recognition epitopes, which is/are derived from the antigen. The antigen-loaded nanogel is administered at least one day prior to administration of antigen-specific T cells to improve the efficacy of a T cell infusion therapy against an immune checkpoint inhibitor-resistant tumor. The hydrophobized polysaccharide may be pullulan having cholesteryl groups bound thereto. An immune-enhancing agent also may be administered in or with the antigen-loaded nanogel.
    Type: Application
    Filed: November 29, 2022
    Publication date: June 29, 2023
    Inventors: Hiroshi SHIKU, Naozumi HARADA, Daisuke MURAOKA, Kazunari AKIYOSHI
  • Publication number: 20220111061
    Abstract: An object is to provide a technique of forming CpG oligonucleotides and hydrophobized polysaccharides into complexes. This object is achieved by a complex comprising a modified CpG oligonucleotide containing a hydrophobic group A having a sterol skeleton, and a modified polysaccharide containing a hydrophobic group B.
    Type: Application
    Filed: September 9, 2021
    Publication date: April 14, 2022
    Applicants: UNITED IMMUNITY, CO., LTD., KYOTO UNIVERSITY
    Inventors: Naozumi HARADA, Kazunari AKIYOSHI, Shin-ichi SAWADA
  • Publication number: 20220062398
    Abstract: A long-chain peptide antigen includes a plurality of epitopes. An interepitope sequence located between two of the plurality of epitopes contains four to ten consecutive tyrosines, threonines, alanines, histidines, glutamines, or asparagines. The killer T-cell recognition epitopes form complexes with MHC class I molecules and are recognized by CD8+ killer T-cells when the complexes are presented on the surfaces of antigen-presenting cells. The helper T-cell recognition epitopes form complexes with MHC class II molecules and are recognized by CD4+ helper T-cells when the complexes are presented on the surfaces of antigen-presenting cells. The peptide is cleaved within the first interepitope sequence upon uptake of the peptide into antigen-presenting cells. The long-chain peptide antigen may be administered to a patient together with a hydrophobized polysaccharide, such as cholesterol-modified pullulan, and/or an adjuvant, such as CpG oligo DNA.
    Type: Application
    Filed: November 18, 2021
    Publication date: March 3, 2022
    Inventors: Hiroshi SHIKU, Naozumi HARADA, Daisuke MURAOKA, Kazunari AKIYOSHI
  • Patent number: 11213538
    Abstract: To provide an agent for overcoming immunosuppression which can overcome immunosuppression by regulatory T cells. An agent for overcoming immunosuppression and an inhibitor of FOXP3 function containing an anthracycline antibiotic as an active ingredient.
    Type: Grant
    Filed: February 15, 2017
    Date of Patent: January 4, 2022
    Assignees: GENERAL INCORPORATED ASSOCIATION PHARMA VALLEY PROJECT SUPPORTING ORGANIZATION, KABUSHIKI KAISHA YAKULT HONSHA
    Inventors: Akira Asai, Naohisa Ogo, Daisuke Muraoka, Hiroshi Shiku, Naozumi Harada
  • Patent number: 11179450
    Abstract: A long-chain peptide antigen includes a plurality of epitopes. An interepitope sequence located between two of the plurality of epitopes contains four to ten consecutive tyrosines. The long-chain peptide antigen may be administered to a patient together with a hydrophobized polysaccharide, such as cholesterol-modified pullulan, and/or an adjuvant, such as CpG oligo DNA.
    Type: Grant
    Filed: July 16, 2018
    Date of Patent: November 23, 2021
    Assignees: MIE UNIVERSITY, KYOTO UNIVERSITY
    Inventors: Hiroshi Shiku, Naozumi Harada, Daisuke Muraoka, Kazunari Akiyoshi
  • Patent number: 11083744
    Abstract: Therapeutic agents effective for treating cell-proliferative diseases contain extracellular vesicles (exosomes) released from cytotoxic T cells or miRNA obtained from extracellular vesicles (exosomes) released from cytotoxic T cells, such as human CD8+ T cells. Such therapeutic agents suppress the proliferation of mesenchymal cells surrounding cancer cells, e.g., by killing the mesenchymal cells, such that the cancer cells become isolated and unable to metastasize. Cell-proliferative diseases are thus treatable by administering such a therapeutic agent to a patient.
    Type: Grant
    Filed: March 18, 2016
    Date of Patent: August 10, 2021
    Assignees: MIE UNIVERSITY, KYOTO UNIVERSITY
    Inventors: Hiroshi Shiku, Naohiro Seo, Kazunari Akiyoshi, Naozumi Harada, Fumiyasu Momose
  • Publication number: 20190111078
    Abstract: An antigen-loaded nanogel is formed by loading or encapsulating one or more long peptide antigens or one or more protein antigens in a hydrophobized polysaccharide. The long peptide antigen(s) or protein antigen(s) contains (or each contain) one or more CD8+ cytotoxic T cell recognition epitopes and/or one or more CD4+ helper T cell recognition epitopes, which is/are derived from the antigen. The antigen-loaded nanogel may be administered prior to administration of antigen-specific T cells to improve the efficacy of a T cell infusion therapy against an immune checkpoint inhibitor-resistant tumor. The hydrophobized polysaccharide may be pullulan having cholesteryl groups bound thereto. An immune-enhancing agent also may be administered in or with the antigen-loaded nanogel.
    Type: Application
    Filed: February 8, 2017
    Publication date: April 18, 2019
    Applicants: MIE UNIVERSITY, KYOTO UNIVERSITY
    Inventors: Hiroshi SHIKU, Naozumi HARADA, Daisuke MURAOKA, Kazunari AKIYOSHI
  • Publication number: 20190038645
    Abstract: To provide an agent for overcoming immunosuppression which can overcome immunosuppression by regulatory T cells. An agent for overcoming immunosuppression and an inhibitor of FOXP3 function containing an anthracycline antibiotic as an active ingredient.
    Type: Application
    Filed: February 15, 2017
    Publication date: February 7, 2019
    Applicants: GENERAL INCORPORATED ASSOCIATION PHARMA VALLEY PROJECT SUPPORTING ORGANIZATION, KABUSHIKI KAISHA YAKULT HONSHA
    Inventors: Akira ASAI, Naohisa OGO, Daisuke MURAOKA, Hiroshi SHIKU, Naozumi HARADA
  • Publication number: 20190015490
    Abstract: A long-chain peptide antigen includes a plurality of epitopes. An interepitope sequence located between two of the plurality of epitopes contains four to ten consecutive tyrosines. The long-chain peptide antigen may be administered to a patient together with a hydrophobized polysaccharide, such as cholesterol-modified pullulan, and/or an adjuvant, such as CpG oligo DNA.
    Type: Application
    Filed: July 16, 2018
    Publication date: January 17, 2019
    Inventors: Hiroshi SHIKU, Naozumi HARADA, Daisuke MURAOKA, Kazunari AKIYOSHI
  • Publication number: 20180177816
    Abstract: Therapeutic agents effective for treating cell-proliferative diseases contain extracellular vesicles (exosomes) released from cytotoxic T cells or miRNA obtained from extracellular vesicles (exosomes) released from cytotoxic T cells, such as human CD8+ T cells. Such therapeutic agents suppress the proliferation of mesenchymal cells surrounding cancer cells, e.g., by killing the mesenchymal cells, such that the cancer cells become isolated and unable to metastasize. Cell-proliferative diseases are thus treatable by administering such a therapeutic agent to a patient.
    Type: Application
    Filed: March 18, 2016
    Publication date: June 28, 2018
    Inventors: Hiroshi SHIKU, Naohiro SEO, Kazunari AKIYOSHI, Naozumi HARADA, Fumiyasu MOMOSE
  • Publication number: 20160367651
    Abstract: A vaccine contains a long-chain peptide antigen having a plurality of epitopes. An interepitope sequence located between two of the plurality of epitopes contains two to ten consecutive tyrosines, two to ten consecutive threonines, two to ten consecutive alanines, two to ten consecutive histidines, two to ten consecutive glutamines or two to ten consecutive asparagines. The vaccine may be an anticancer vaccine, an antibacterial vaccine or an antiviral vaccine. The vaccine may be a peptide vaccine, a DNA vaccine, an mRNA vaccine or a dendritic cell vaccine.
    Type: Application
    Filed: October 1, 2014
    Publication date: December 22, 2016
    Inventors: Hiroshi SHIKU, Naozumi HARADA, Daisuke MURAOKA, Kazunari AKIYOSHI
  • Publication number: 20140322344
    Abstract: A vaccine preparation for treating cancer includes a complex of a hydrophobized polysaccharide and at least one synthetic long peptide derived from a tumor-specific antigenic protein and/or a pathogen-derived antigenic protein. The at least one synthetic long peptide contains at least one CD8+ cytotoxic T-cell recognition epitope and at least one CD4+ helper T-cell recognition epitope. The complex is simultaneously administered to the patient with at least one immunopotentiating agent.
    Type: Application
    Filed: August 30, 2012
    Publication date: October 30, 2014
    Applicants: National University Corporation Tokyo Medical and Dental University, MIE University
    Inventors: Hiroshi Shiku, Naozumi Harada, Daisuke Muraoka, Kazunari Akiyoshi
  • Publication number: 20120029175
    Abstract: A process for producing an embedded protein antigen, comprising embedding a protein antigen having two or more cysteine residues in a molecule thereof, into a hydrophobized polysaccharid. Prior to or after the embedding of the protein antigen, the protein antigen is purified. There are provided an embedded protein antigen and a process for producing the same, which can advantageously purify the protein antigen, while suppressing the denaturation of the protein antigen as completely as possible.
    Type: Application
    Filed: April 11, 2007
    Publication date: February 2, 2012
    Inventors: Kenji Nagura, Naozumi Harada, Masahiro Urushihara