• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

Evaluation of new type of vaccine strategy against infectious diseases

Research Project

Project/Area Number 15K09590
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Infectious disease medicine
Research InstitutionInstitute of Physical and Chemical Research

Principal Investigator

Shimizu Kanako  国立研究開発法人理化学研究所, 統合生命医科学研究センター, 上級研究員 (20391980)

Co-Investigator(Kenkyū-buntansha) 藤井 眞一郎  国立研究開発法人理化学研究所, その他, 研究員 (10392094)
山崎 哲  国立研究開発法人理化学研究所, その他, 研究員 (30392161)
Project Period (FY) 2015-04-01 – 2018-03-31
Project Status Completed (Fiscal Year 2017)
Budget Amount *help
¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2017: ¥650,000 (Direct Cost: ¥500,000、Indirect Cost: ¥150,000)
Fiscal Year 2016: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2015: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
Keywordsin vivo DC targeting / NKT / antibody / CD4Tfh / influenza / NKT細胞 / 樹状細胞 / CD4Tfh細胞 / 抗体
Outline of Final Research Achievements

The goal of vaccines against infectious diseases is to induce long-term cellular and humoral immunity. Development of synthetic anti-viral vaccines that trigger CD4+ T cell-dependent B cell immune responses has been attempted. Here, we show, using a cellular vaccine carrying foreign protein antigen plus iNKT cell glycolipid antigen, designated as artificial adjuvant vector cells (aAVCs), that mature DCs in situ elicit not only ordinal antigen-specific CD4+ T cells, but also CD4+ Tfh and germinal center, resulted in inducing long-term antibody production. As a mechanism, CD4+ Tfh cells, but not Bcl6-/- CD4+ T or iNKTfh cells played an important role. To develop it for influenza infection, we established influenza hemagglutinin-carrying aAVC (aAVC-HA) and found that all the mice vaccinated with aAVC-HA were protected from influenza infection. Thus, the in vivo DC targeting therapy by aAVC would be useful for protection against viral infection.

Report

(4 results)
  • 2017 Annual Research Report   Final Research Report ( PDF )
  • 2016 Research-status Report
  • 2015 Research-status Report
  • Research Products

    (11 results)

All 2018 2017 2016 2015

All Journal Article (7 results) (of which Peer Reviewed: 4 results,  Open Access: 2 results,  Acknowledgement Compliant: 3 results) Presentation (4 results) (of which Int'l Joint Research: 1 results)

  • [Journal Article] NK, NKT細胞について教えてください2018

    • Author(s)
      5.清水佳奈子
    • Journal Title

      がん免疫療法 Cancer Immunotherapy

      Volume: 2

    • Related Report
      2017 Annual Research Report
  • [Journal Article] Exploiting antitumor immunotherapeutic novel strategies by deciphering the cross talk between invariant NKT cells and dendritic cells.2017

    • Author(s)
      Fujii S and Shimizu K
    • Journal Title

      Front Immunol.

      Volume: 8

    • DOI

      10.3389/fimmu.2017.00886

    • Related Report
      2017 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] 最近の樹状細胞の基礎的知見から次世代樹状細胞標的療法への展望2017

    • Author(s)
      藤井眞一郎、山崎哲、伊豫田智典、清水佳奈子
    • Journal Title

      臨床免疫・アレルギー科

      Volume: 67 Pages: 560-566

    • Related Report
      2017 Annual Research Report
  • [Journal Article] がん免疫における樹状細胞の役割2017

    • Author(s)
      藤井 眞一郎、山崎哲、清水佳奈子
    • Journal Title

      炎症と免疫

      Volume: 25 Pages: 66-71

    • Related Report
      2017 Annual Research Report
  • [Journal Article] In vivo dendritic cell targeting cellular vaccine induces CD4+ Tfh cell-dependent antibody against influenza virus.2016

    • Author(s)
      Yamasaki S, Shimizu K, Kometani K, Sakurai M, Kawamura M, and Fujii S*.
    • Journal Title

      Sci Rep

      Volume: 6 Issue: 1 Pages: 35173-35173

    • DOI

      10.1038/srep35173

    • Related Report
      2016 Research-status Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Journal Article] Systemic DC activation modulates the tumor microenvironment and shapes the long-lived tumor-specific memory mediated by CD8+ T cells.2016

    • Author(s)
      Shimizu K, Yamasaki S, Shinga J, Sato Y, Watanabe T, Ohara O, Kuzushima K, Yagita H, Komuro Y, Asakura M, Fujii S
    • Journal Title

      Cancer Res

      Volume: 76(13) Issue: 13 Pages: 3756-3766

    • DOI

      10.1158/0008-5472.can-15-3219

    • Related Report
      2016 Research-status Report
    • Peer Reviewed / Acknowledgement Compliant
  • [Journal Article] Systemic DC activation modulates the tumor microenvironment and shapes the long-lived tumor-specific memory mediated by CD8+ T cells2016

    • Author(s)
      Kanako Shimizu, Satoru Yamasaki, Jun Shinga, Yusuke Sato, Takashi Watanabe, Osamu Ohara, Kiyotaka Kuzushima, Hideo Yagita, Yoshiko Komuro, Miki Asakura, and Shin-ichiro Fujii
    • Journal Title

      Cancer Research

      Volume: in press

    • Related Report
      2015 Research-status Report
    • Peer Reviewed / Acknowledgement Compliant
  • [Presentation] “Systemic and potent DC activation modulates the tumor microenvironment and shapes the long-lived tumor-specific memory T cells”2017

    • Author(s)
      Kanako Shimizu
    • Organizer
      The 75th Annual meeting of the Japanese Cancer association,
    • Place of Presentation
      Pacifico Yokohama, Yokohama, Japan
    • Related Report
      2016 Research-status Report
  • [Presentation] “Transfer of mRNA encoding invariant NKT cell receptors imparts glycolipid specific responses to T cells and γδT cells”2017

    • Author(s)
      Kanako Shimizu
    • Organizer
      The 8th Annual Meeting of Society of Immunotherapy for Hematological Disorders
    • Place of Presentation
      The Alumni Hall ”Frate” , Hokkaido University, Sapporo, Japan
    • Related Report
      2016 Research-status Report
  • [Presentation] Strong antitumor response and immunological memory elicited by NKT cell-licensed, tumor antigen captured DCs in situ as a new type of cancer vaccine2015

    • Author(s)
      Kanako Shimizu
    • Organizer
      The 44th Annual Meeting of The Japanese Society for Immunology
    • Place of Presentation
      札幌コンベンションセンター(北海道・札幌)
    • Year and Date
      2015-11-20
    • Related Report
      2015 Research-status Report
  • [Presentation] Strong antitumor response and immunological memory immunity elicited by NKT cell-licensed, tumor antigen captured DCs in situ as a new type of cancer vaccine2015

    • Author(s)
      Kanako Shimizu
    • Organizer
      Cell Symposia
    • Place of Presentation
      Sitges, Spain
    • Year and Date
      2015-06-15
    • Related Report
      2015 Research-status Report
    • Int'l Joint Research

URL: 

Published: 2015-04-16   Modified: 2019-03-29  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi