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Mechanisms of blister formation in pemphigus foliacues analyzed by anti-Dsg1 monoclonal antibodies

Research Project

Project/Area Number 15K09749
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Dermatology
Research InstitutionToho University

Principal Investigator

ISHII Ken  東邦大学, 医学部, 准教授 (50296670)

Co-Investigator(Kenkyū-buntansha) 石河 晃  東邦大学, 医学部, 教授 (10202988)
Research Collaborator YOSHIDA Kenji  
Project Period (FY) 2015-04-01 – 2018-03-31
Project Status Completed (Fiscal Year 2017)
Budget Amount *help
¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2017: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2016: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2015: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Keywords天疱瘡 / 自己抗体 / 細胞接着 / カドヘリン / 自己免疫
Outline of Final Research Achievements

Pemphigus foliaceus (PF) is an autoimmune blistering disease caused by autoantibodies (Abs) against desmoglein 1 (Dsg1). PF sera contain polyclonal Abs which are heterogeneous mixture of both pathogenic and non-pathogenic Abs, as shown by isolation of monoclonal Abs (mAbs).The purpose of study is to investigate how pathogenic and non-pathogenic anti-Dsg1 Abs contribute to blister formation in PF. Using organ-cultured human skin, we compared the effect of a single pathogenic anti-Dsg1 IgG mAb, a single non-pathogenic anti-Dsg1 IgG mAb, and their mixture on blister formation as analyzed by histology, subcellular localization of IgG deposits and desmosomal proteins by confocal microscopy. We found a polyclonal mixture of anti-Dsg1 IgG antibodies enhances pathogenic activity for blister formation associated with p38MAPK-dependent Dsg1 clustering and that not only pathogenic antibodies but also non-pathogenic antibodies coordinately contribute to blister formation in PF.

Report

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

    (7 results)

All 2018 2017 2016 2015

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

  • [Journal Article] Splice site mutation in COL7A1 resulting in aberrant in-frame transcripts identified in a case of recessive dystrophic epidermolysis bullosa, pretibial2018

    • Author(s)
      Masunaga Takuji、Kubo Akiharu、Ishiko Akira
    • Journal Title

      The Journal of Dermatology

      Volume: 45 Issue: 6 Pages: 306-307

    • DOI

      10.1111/1346-8138.14271

    • Related Report
      2017 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Alopecia developed in a transitional case from pemphigus foliaceus to pemphigus vulgaris2017

    • Author(s)
      Yoshida Kenji、Ishii Ken、Ishiko Akira
    • Journal Title

      The Journal of Dermatology

      Volume: 44 Issue: 11

    • DOI

      10.1111/1346-8138.13957

    • Related Report
      2017 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Non-pathogenic pemphigus foliaceus (PF) IgG acts synergistically with a directly pathogenic PF IgG to increase blistering by p38MAPK-dependent desmoglein 1 clustering2017

    • Author(s)
      Yoshida K, Ishii K, Shimizu A, Yokouchi M, Amagai M, Shiraishi K, Shirakata Y, Stanley JR, Ishiko A.
    • Journal Title

      J Dermatol Sci

      Volume: 85 Issue: 3 Pages: 197-207

    • DOI

      10.1016/j.jdermsci.2016.12.010

    • Related Report
      2016 Research-status Report
    • Peer Reviewed / Open Access / Int'l Joint Research / Acknowledgement Compliant
  • [Presentation] Desmoglein 1 clustering in pemphigus foliaceus patients’ skin.2017

    • Author(s)
      Kenji Yoshida, Ken Ishii1, Mari Nakagawa, Akira Ishiko
    • Organizer
      Tne 42nd Annual Meeting of the Japanese Society for Investigative Dermatology
    • Related Report
      2017 Annual Research Report
    • Int'l Joint Research
  • [Presentation] p38MAPK contributes to loss of cell adhesion through clustering of desmoglein 1 but is not required for blistering in pemphigus foliaceus .2016

    • Author(s)
      Yoshida K , Ishii K, Shimizu A , Yokouchi M , Amagai M ,John R.Stanley, Ishiko A
    • Organizer
      第41回日本研究皮膚科学会学術大会
    • Place of Presentation
      仙台国際センター(宮城県仙台市)
    • Year and Date
      2016-12-09
    • Related Report
      2016 Research-status Report
  • [Presentation] Polyclonal nature of pemphigus foliaceus IgG antibodies enhances pathogenic effect for blister formation in association with p38MAPK-dependent desmoglein 1 clustering.2016

    • Author(s)
      Yoshida K, Ishii K , Shimizu A , Yokouchi M , Amagai M ,John R.Stanley , Ishiko A
    • Organizer
      Pathogenesis of pemphigus and pemhigoid 2016 the open blister/mind meeting,
    • Place of Presentation
      ミュンヘン大学(ドイツ、ミュンヘン)
    • Year and Date
      2016-09-07
    • Related Report
      2016 Research-status Report
  • [Presentation] p38 MAPK signaling is necessary for desmoglein 1 clustering and enhances pathogenic effect, but is not required for blistering in pemphigus foliaceus2015

    • Author(s)
      Yoshida K, Ishii K, Shimizu A, Yokouchi M, Amagai M, Stanley JR, Ishiko A
    • Organizer
      45th Annual European Society of Dermatological Research Meeting
    • Place of Presentation
      オランダ、ロッテルダム
    • Year and Date
      2015-09-12
    • Related Report
      2015 Research-status Report
    • Int'l Joint Research

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

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