Yoshioka, Yasuo

Profile

Dr. Yoshioka received his Ph.D. from Osaka University in 2004. He took his current positon at RIMD from 2015 after working at National Institute of Health Sciences, the Center for Advanced Medical Engineering and Informatics and Grad. School of Pharmaceutical Sciences in Osaka University.

Publication

  • (1) Inflammatory mediators of mRNA vaccine-induced adverse reactions in mice. Honda K. et. al. Mol Ther. (2026)S1525-0016(26)00023-7.
  • (2) mRNA vaccine expressing enterovirus D68 virus-like particles induces potent neutralizing antibodies and protects against infection. Kunishima Y. et. al. Mol Ther Nucleic Acids. (2025)36(4):102731.
  • (3) Modulating Immunogenicity and Reactogenicity in mRNA-Lipid Nanoparticle Vaccines through Lipid Component Optimization. Kawaguchi Y. et. al. ACS Nano. (2025)19(30):27977-28001.
  • (4) Hypertonic intranasal vaccines gain nasal epithelia access to exert strong immunogenicity. Hashimoto S. et. al. Mucosal Immunol. (2025)S1933-0219(25)00032-7.
  • (5) Low-inflammatory lipid nanoparticle-based mRNA vaccine elicits protective immunity against H5N1 influenza virus with reduced adverse reactions. Kawai A. et. al. Mol Ther. (2025)33(2):529-547.
  • (6) Recombinant RSV G protein vaccine induces enhanced respiratory disease via IL-13 and mucin overproduction. Kawahara E. et. al. NPJ Vaccines. (2024)9(1):187.
  • (7) Lipid Nanoparticle with 1,2-Di-O-octadecenyl-3-trimethylammonium-propane as a Component Lipid Confers Potent Responses of Th1 Cells and Antibody against Vaccine Antigen. Kawai A. et. al. ACS Nano. (2024)18(26):16589-16609.
  • (8) Intranasal immunization with an RBD-hemagglutinin fusion protein harnesses preexisting immunity to enhance antigen-specific responses. Kawai A. et. al. J Clin Invest. (2023)133(23):e166827.
  • (9) Upregulation of Robo4 expression by SMAD signaling suppresses vascular permeability and mortality in endotoxemia and COVID-19 models. Morita M. et. al. Proc Natl Acad Sci USA. (2023)120(3):e2213317120.
  • (10) SARS-CoV-2 disrupts respiratory vascular barriers by suppressing Claudin-5 expression. Hashimoto R. et. al. Sci Adv. (2022)8(38):eabo6783.
  • (11) Elucidation of the role of nucleolin as a cell surface receptor for nucleic acid-based adjuvants. Kitagawa S. et. al. NPJ Vaccines. (2022)7(1):115.
  • (12) Efficient antigen delivery by dendritic cell-targeting peptide via nucleolin confers superior vaccine effects in mice. Matsuda T. et. al. iScience. (2022)25(11):105324.
  • (13) The potential of neuraminidase as an antigen for nasal vaccines to increase cross-protection against influenza viruses. Kawai A. et. al. J Virol. (2021)95(20):e0118021.
  • (14) Synergistic effect of non-neutralizing antibodies and interferon-γ for cross-protection against influenza. Shibuya M. et. al. iScience. (2021)24(10):103131.
  • (15) Neutrophil-Mediated Lung Injury Both via TLR2-Dependent Production of IL-1α and IL-12 p40, and TLR2-Independent CARDS Toxin after Mycoplasma pneumoniae Infection in Mice. Tamiya S. et. al. Microbiol Spectr. (2021)9(3):e0158821.
  • (16) Murine cross-reactive non-neutralizing polyclonal IgG1 antibodies induced by influenza vaccine inhibit the cross-protective effect of IgG2 against heterologous virus in mice. Shibuya M. et. al. J Virol. (2020)94(12):e00323-20.

Lab

Abe, Ryuichiro

International Research Center for Infectious Diseases

Laboratory of Bacterial Pathogenesis

Akira, Shizuo

Division of Host Defense

Department of Host Defense

Arase, Hisashi

Division of Host Defense

Department of Immunochemistry

Ebina, Hirotaka

BIKEN Innovative Vaccine Research Alliance Laboratories

Virus Vaccine Group

Fujimoto, Kosuke

Division of Infectious Disease

Department of Microbial Regulation

Hara, Eiji

Division of Cellular and Molecular Biology

Department of Molecular Biology

Horii, Toshihiro

Research Center for Infectious Disease Control

Laboratory of Malaria Vaccine Development

Iida, Tetsuya

Research Center for Infectious Disease Control

Department of Bacterial Infections

Ikawa, Masahito

Bioinformatics Center

Department of Experimental Genome Research

Ishitani, Tohru

Division of Cellular and Molecular Biology

Department of Homeostatic Regulation

Iwanaga, Shiroh

Research Center for Infectious Disease Control

Department of Molecular Protozoology

Iwasaki, Masaharu

International Research Center for Infectious Diseases

Laboratory of Emerging Viral Diseases

Kenji Kamimoto

Division of Cellular and Molecular Biology

Department of Systems Biomedical Science

Kobayashi, Takeshi

Research Center for Infectious Disease Control

Department of Virology

Kotani, Ai

Division of Cellular and Molecular Biology

Department of Regulation of Infectious Cancer

Matsuura, Yoshiharu

Research Center for Infectious Disease Control

Laboratory of Virus Control

Murakami, Yoshiko

Division of Host Defense

Laboratory of Immunoglycobiology

Nakamura, Shota

Bioinformatics Center

Department of Infection Metagenomics

Nakatani, Yoichiro

Bioinformatics Center

Department of Biological Informatics Laboratory of Medical and Evolutionary Genomics

Standley, Daron

Bioinformatics Center

Department of Genome Informatics

Suzuki, Kazuhiro

Division of Host Defense

Department of Immune Response Dynamics

Takakura, Nobuyuki

Division of Cellular and Molecular Biology

Department of Signal Transduction

Tsukamoto, Kentaro

International Research Center for Infectious Diseases

Laboratory of Bacterial Zoonoses

Watanabe, Tokiko

Division of Infectious Disease

Department of Molecular Virology

Yamamoto, Masahiro

Division of Infectious Disease

Department of Immunoparasitology

Yamasaki, Sho

Division of Host Defense

Department of Molecular Immunology

Yamasaki, Shotaro

Bioinformatics Center

Department of Biological Informatics Laboratory of RNA Informatics