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Preparation of sialylated IgG and elucidation of the mechanism for its anti-inflammatory properties

Research Project

Project/Area Number 23590578
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Immunology
Research InstitutionNational Hospital Organization,Yamaguchi - Ube Medical Center

Principal Investigator

MIMURA YUSUKE  独立行政法人国立病院機構山口宇部医療センター(臨床研究部), その他部局等, 研究員 (00219718)

Project Period (FY) 2011 – 2013
Project Status Completed (Fiscal Year 2013)
Budget Amount *help
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2013: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2012: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2011: ¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
KeywordsIgG / glycosylation / sialylation / DC-SIGN / Glycosylation / Sialylation / Fc / ADCC
Research Abstract

The attachment of oligosaccharide, at Asn297, of the IgG-Fc heavy chain is essential for optimal activation of Fc effector functions. It has recently been shown that IgG with oligosaccharides bearing terminal sialic acid residues mediates anti-inflammatory therapeutic effects. We expressed an IgG1 Phe243Ala (F243A) mutant in both human and rodent cell lines, and sialylation was found to be markedly increased. The mechanism by which the sialic acid residues in the IgG-Fc oligosaccharides exert an anti-inflammatory effect has been investigated by using dendritic cells that express DC-SIGN.

Report

(4 results)
  • 2013 Annual Research Report   Final Research Report ( PDF )
  • 2012 Research-status Report
  • 2011 Research-status Report
  • Research Products

    (4 results)

All 2013

All Presentation (4 results)

  • [Presentation] Increased sialylation of a recombinant IgG mutant produced in human embryonic kidney 293 (HEK293) cells2013

    • Author(s)
      Mimura, Y, et al.
    • Organizer
      15th International Congress of Immunology
    • Place of Presentation
      Milan
    • Related Report
      2013 Final Research Report
  • [Presentation] Enhanced sialylation of a mouse-human chimeric IgG1 antibody produced in human embryonic kidney 293 (HEK293) cells2013

    • Author(s)
      Mimura, Y, et al.
    • Organizer
      第42回日本免疫学会学術集会
    • Place of Presentation
      千葉
    • Related Report
      2013 Final Research Report
  • [Presentation] Increased sialylation of a recombinant IgG mutant produced in human embryonic kidney 293 (HEK293) cells2013

    • Author(s)
      Yusuke Mimura
    • Organizer
      15th International Congress of Immunology
    • Place of Presentation
      Italy, Milan
    • Related Report
      2013 Annual Research Report
  • [Presentation] Enhanced sialylation of a mouse-human chimeric IgG1 antibody produced in human embryonic kidney 293 (HEK293) cells2013

    • Author(s)
      三村雄輔
    • Organizer
      第42回日本免疫学会学術集会
    • Place of Presentation
      千葉、幕張メッセ
    • Related Report
      2013 Annual Research Report

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Published: 2011-08-05   Modified: 2019-07-29  

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