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Research on the immune system in uninfected cells that defines the immune response during viral infection

Research Project

Project/Area Number 18K07162
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Review Section Basic Section 49070:Immunology-related
Research InstitutionKobe University

Principal Investigator

Kameyama Takeshi  神戸大学, 医学研究科, 特命助教 (40569505)

Co-Investigator(Kenkyū-buntansha) 高岡 晃教  北海道大学, 遺伝子病制御研究所, 教授 (30323611)
山田 大翔  北海道大学, 遺伝子病制御研究所, 助教 (10779333)
佐藤 精一  北海道大学, 遺伝子病制御研究所, 講師 (60459724)
Project Period (FY) 2018-04-01 – 2021-03-31
Project Status Completed (Fiscal Year 2020)
Budget Amount *help
¥4,420,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥1,020,000)
Fiscal Year 2020: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2019: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2018: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Keywords自然免疫 / ウイルス / インターフェロン / シグナル伝達
Outline of Final Research Achievements

Interferons (IFNs) are the main cytokines for the innate immune response against viral infection. It is known that IFNs are constitutively induced at very low levels in the absence of viral infection. These constitutively induced IFNs and their signals are essential for the rapid and robust induction of IFN induction after viral infection and for the suppression of carcinogenesis. However, the mechanism of this constitutive IFN induction and its regulation remains unclear. In this study, we found that the constitutive IFNs are induced through an intracellular RNA sensor-dependent recognition of endogenous RNAs and the downstream signaling pathway. Furthermore, we found several regulatory factors that regulate cytosolic nucleic acid-mediated innate immune responses. These results identified a novel regulatory mechanism that controls constitutively induced IFNs, which may provide a novel prophylactic target for viral control and suppression of carcinogenesis.

Academic Significance and Societal Importance of the Research Achievements

本研究ではウイルスに対する免疫応答を規定する非感染状態の免疫システムが内因性RNAによって構成的なIFNが制御されていることを明らかにしたという学術的意義がある.構成的IFNは,
感染症予防や発がん制御に重要であることが知られているので,本研究成果はこれまでにない新しいアプローチから感染症予防や発がん制御という領域を構築するための分子基盤となると期待される.近年地球温暖化やグローバル社会により様々な感染症リスクが増加し,現在コロナ禍で世界中が脅威にさらされており,加えて超高齢化社会となった日本において,予防的な観点から感染対策や抗がん対策を行うことは責務の課題であり社会的意義が高い.

Report

(4 results)
  • 2020 Annual Research Report   Final Research Report ( PDF )
  • 2019 Research-status Report
  • 2018 Research-status Report
  • Research Products

    (3 results)

All 2020 2019 2018

All Journal Article (2 results) (of which Peer Reviewed: 2 results,  Open Access: 2 results) Presentation (1 results)

  • [Journal Article] Regulation of an adaptor protein STING by Hsp90β to enhance innate immune responses against microbial infections2020

    • Author(s)
      Seiichi Sato, Kai Li, Nozomi Sakurai, Mei Hashizume, Sunanda Baidya, Hirotaka Nonaka, Koki Noguchi, Kozo Ishikawa, Chikashi Obuse, Akinori Takaoka
    • Journal Title

      Cellular Immunology

      Volume: 356 Pages: 104188-104188

    • DOI

      10.1016/j.cellimm.2020.104188

    • Related Report
      2020 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] BinCARD2 as a positive regulator of interferon response in innate immunity2019

    • Author(s)
      Suzuki Hiraku、Kameyama Takeshi、Takaoka Akinori
    • Journal Title

      Biochemical and Biophysical Research Communications

      Volume: 511 Issue: 2 Pages: 287-293

    • DOI

      10.1016/j.bbrc.2019.02.029

    • Related Report
      2018 Research-status Report
    • Peer Reviewed / Open Access
  • [Presentation] 癌細胞におけるIL-32の直接的な作用の検討2018

    • Author(s)
      郷 俊寛、亀山 武志、高岡 晃教
    • Organizer
      第22回日本がん免疫学会
    • Related Report
      2018 Research-status Report

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Published: 2018-04-23   Modified: 2022-01-27  

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