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Ex-vivo pretreatment of islets with Mitomycin-C have a potential to induce specific immune response for peripheral tolerance

Research Project

Project/Area Number 17K16512
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field General surgery
Research InstitutionFukushima Medical University

Principal Investigator

Sato Naoya  福島県立医科大学, 医学部, 助教 (90622332)

Project Period (FY) 2017-04-01 – 2019-03-31
Project Status Completed (Fiscal Year 2018)
Budget Amount *help
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2018: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2017: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Keywords膵島移植 / 免疫寛容 / preconditioning / Mitomycin-C / Mitomysin-C / 前処置 / 樹状細胞
Outline of Final Research Achievements

Introduction: Our previous study demonstrated that ex-vivo Mitomycin-C(MMC) pretreatment of islets reduced immunogenicity, enhancing graft survival without immunosuppression. The aim of this study is to investigate an immunological mechanism to enhance graft survival of MMC-treated islets. Methold:Isolated islets with MMC pretreatment were implanted to renal subcapsular space of diabetic mice. Immune response to xenograft in over-100-days after grafting was evaluated by histological analysis.Result:Histological and immunohistochemical analyses of the implant site revealed that infiltration of CD3-positive T cell was decreased in MMC-treated islets in early phase after transplantation. In all mice survived over-100-days, CD3-positive T cell aggregation surround by CD45R-positive B cell was found near xenograft. Conclusion: Ex-vivo MMC pretreatment of islets reduced early phase immune response to xenograft and induced characteristic immune response in peripheral transplantation site.

Academic Significance and Societal Importance of the Research Achievements

移植後免疫抑制剤を加えずに、移植前処置のみでグラフトの長期生着をもたらすプロトコールの確立は、膵島移植のみならず移植医療の究極的な目標である。我々の既報ではMMC処置によるSublethal cell stressは細胞死を回避し、免疫応答の抑制により膵島移植片の生着率の改善をもたらしている。これは移植前処置における理想的な免疫抑制モデルとなる可能性を秘めており、この細胞死の回避と免疫寛容メカニズムを解明する事により、最適な移植前処置の確立と膵島移植成績の向上へつながるものと期待される。

Report

(3 results)
  • 2018 Annual Research Report   Final Research Report ( PDF )
  • 2017 Research-status Report
  • Research Products

    (4 results)

All 2018 2017

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

  • [Journal Article] Ex vivo Pretreatment of Islets with Mitomycin C2017

    • Author(s)
      Sato Naoya、Haga Junichiro、Anazawa Takayuki、Kenjo Akira、Kimura Takashi、Wada Ikuo、Mori Tsutomu、Marubashi Shigeru、Gotoh Mitsukazu
    • Journal Title

      Cell Transplantation

      Volume: 26 Issue: 8 Pages: 1392-1404

    • DOI

      10.1177/0963689717721233

    • Related Report
      2017 Research-status Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Presentation] Ex-vivo pretreatment of islets with Mitomycin-C have a potential to induce specific immune response for peripheral tolerance.2018

    • Author(s)
      Naoya Sato, Akira Kenjo, Takashi Kimura, Ryo Okada, Terushige Ishigame, Yasuhide Kofunato, Junichiro Watanabe, Makoto Muto, Seiko Suzushino, Shigeru Marubashi
    • Organizer
      American transplant congress 2018
    • Related Report
      2018 Annual Research Report
    • Int'l Joint Research
  • [Presentation] 移植前Mitomycin-C処置に対する末梢性免疫寛容性免疫応答の検討2018

    • Author(s)
      佐藤直哉 岡田良 石亀輝英 小船戸康英 渡邊淳一郎 武藤亮 鈴志野聖子 月田茂之  木村隆 見城明 志村龍男 丸橋繁
    • Organizer
      日本移植学会
    • Related Report
      2018 Annual Research Report
  • [Presentation] Ex-Vivo Pretreatment of Islets with Mitomycin-C Have a Potential to Induce Specific Immune Response for Peripheral Tolerance2018

    • Author(s)
      Naoya Sato, Akira Kenjo, Takashi Kimura, Ryo Okada, Terushige Ishigame, Yasuhide Kofunato, Junichiro Watanabe, Makoto Muto, Seiko Suzushino, Shigeru Marubashi
    • Organizer
      American Transplant Congress
    • Related Report
      2017 Research-status Report
    • Int'l Joint Research

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Published: 2017-04-28   Modified: 2020-03-30  

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