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Development of anti-IL-33 agent and application for prevention of early allergic disease

Research Project

Project/Area Number 26670057
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Drug development chemistry
Research InstitutionKumamoto University

Principal Investigator

Shoji Shozo  熊本大学, 大学院生命科学研究部(薬), 名誉教授 (60040317)

Project Period (FY) 2014-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Fiscal Year 2015: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
KeywordsIL-33
Outline of Final Research Achievements

IL-33, a member of IL-1 family, is deeply associated with allergic reactions. In this study, we explored the anti-IL-33 agents. We established an in vitro assay system using KU812 cells that are known as immature human basophilic cell line to investigate the anti-IL-33 agents. Reported crystallographic structure of complex of IL-33 and the receptor ST2L was referred to select already known compounds or to synthesized novel compounds for the evaluation. As a result, two novel compounds, named Fi-10 and Fi-11, interestingly showed highest anti-IL-33 activity in the examined compounds in this study. It was suggested that the two compounds directly act to IL-33 to inhibit the activity. Further optimization of the chemical structure based on our results should be required to develop highly specific anti-IL-33 agents in the future.

Report

(3 results)
  • 2015 Annual Research Report   Final Research Report ( PDF )
  • 2014 Research-status Report
  • Research Products

    (5 results)

All 2015 2014

All Journal Article (1 results) (of which Peer Reviewed: 1 results,  Acknowledgement Compliant: 1 results) Presentation (4 results)

  • [Journal Article] N-myristoyltransferase 1 enhances human immunodeficiency virus replication through regulation of viral RNA expression level.2015

    • Author(s)
      Ohta H, Takamune N, Kishimoto N, Shoji S, Misumi S.
    • Journal Title

      Biochem. Biophys. Res. Commun.

      Volume: 463 Issue: 4 Pages: 988-993

    • DOI

      10.1016/j.bbrc.2015.06.047

    • Related Report
      2015 Annual Research Report
    • Peer Reviewed / Acknowledgement Compliant
  • [Presentation] HIV-1 p2 peptideはミトコンドリア呼吸鎖の活性化を介してHIV-1の感染性を増強する2014

    • Author(s)
      竹元 雄輝、小川 実菜子、高宗 暢暁、庄司 省三、三隅 将吾
    • Organizer
      第31回 日本薬学会九州支部大会
    • Place of Presentation
      福岡
    • Year and Date
      2014-12-06 – 2014-12-07
    • Related Report
      2014 Research-status Report
  • [Presentation] 宿主因子GAPDHによるtRNALys3取込み阻害機構の解析2014

    • Author(s)
      岸本 直樹、鬼塚 彩乃、伊賀 望、高宗 暢暁、庄司 省三、三隅 将吾
    • Organizer
      第28回 日本エイズ学会学術集会
    • Place of Presentation
      大阪
    • Year and Date
      2014-12-03 – 2014-12-05
    • Related Report
      2014 Research-status Report
  • [Presentation] Nef mRNAの5'UTRに存在するその効率的な翻訳に必須となるcis領域2014

    • Author(s)
      長峰 啓志郎、高宗 暢暁、庄司 省三、三隅 将吾
    • Organizer
      第87回 日本生化学会大会
    • Place of Presentation
      京都
    • Year and Date
      2014-10-15 – 2014-10-18
    • Related Report
      2014 Research-status Report
  • [Presentation] Glyceraldehyde 3-phosphate dehydrogenaseによるHIV逆転写反応開始阻害機構2014

    • Author(s)
      岸本 直樹、鬼塚 彩乃、伊賀 望、高宗 暢暁、庄司 省三、三隅 将吾
    • Organizer
      第87回 日本生化学会大会
    • Place of Presentation
      京都
    • Year and Date
      2014-10-15 – 2014-10-18
    • Related Report
      2014 Research-status Report

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Published: 2014-04-04   Modified: 2017-05-10  

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