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Suppression of allergy with non-specific monoclonal IgE antibodies.

Research Project

Project/Area Number 10555290
Research Category

Grant-in-Aid for Scientific Research (B).

Allocation TypeSingle-year Grants
Section展開研究
Research Field 生物・生体工学
Research InstitutionOKAYAMA UNIVERSITY

Principal Investigator

OHMORI Hitoshi  Okayama University, Department of Biotechnology, Professor, 工学部, 教授 (70116440)

Co-Investigator(Kenkyū-buntansha) KOMORIYA Keiji  Teijin Institute for Biomedical Research, Depertment of Pharmacology, Director, 医薬開発研究所, 部長
HIKIDA Masaki  Okayama University, Department of Biotechnology, Lecturer, 工学部, 講師 (60228715)
Project Period (FY) 1998 – 2000
Project Status Completed (Fiscal Year 2000)
Budget Amount *help
¥11,800,000 (Direct Cost: ¥11,800,000)
Fiscal Year 2000: ¥2,200,000 (Direct Cost: ¥2,200,000)
Fiscal Year 1999: ¥3,700,000 (Direct Cost: ¥3,700,000)
Fiscal Year 1998: ¥5,900,000 (Direct Cost: ¥5,900,000)
KeywordsAllergy / IgE antibody / hybridoma / monoclonal antibody / RAG genes / V(D)J recombination / nematode / transgenic mouse
Research Abstract

Although a high level of IgE is produced after primary infection with Nippostrongylus brasiliensis (Nb), most of the IgE antibodies (Abs) are not specific to the worm. Analyses with Western blotting and enzyme-linked immunosorbent assay revealed that the IgE Abs from Nb-infected BALB/c mice did not show reactivity with Nb-derived excretory-secretory proteins and antigens present in the cell-free extracts of the worm. Monoclonal IgE Abs obtained from the Nb-infected mice were not reactive with these Nb antigen either. To characterize Nb-induced IgE response, we used (QM x C57BL/6)F1 (QBF1) mice that bear the knock-in 17.2.25 VHDJH segment (VHT) encoding a VH region specific to 4-hydroxy-3-nitrophenylacetyl hapten, and express VHT-encoded antigen receptors on 80-85% of their B cells. Consistent with the frequency of VHT-positive B cells, more than 80% of IgE Abs induced in QBF1 B cells that were cultured with LPS plus IL-4 were found to bear VHT-encoded H chains. In contrast, when QBF1 mice were infected with Nb, less than 10% of Nb-induced IgE Abs were found to use VHT.The QBF1-derived IgE did not react with Nb antigens either. We have shown in mice that B cells reexpress RAG-1 and RAG-2 proteins, and undergo secondary rearrangement of Ig genes (receptor editing) in the periphery. Taken together, data suggest that Nb-induced IgE response in mice is not merely the result of polyclonal activation of B cells, but may involve a mechanism that revise Ig genes secondarily.

Report

(4 results)
  • 2000 Annual Research Report   Final Research Report Summary
  • 1999 Annual Research Report
  • 1998 Annual Research Report
  • Research Products

    (22 results)

All Other

All Publications (22 results)

  • [Publications] Masaki Hikida: "Rerrangement of λ light chain genes in mature B cells in vitro and in vivo. Function of reexpressed recombination-activating gene (RAG) products."Journal of Experimental Medicine. 187. 795-799 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Hitoshi Ohmori: "Expression and function of recombination activating genes in mature B cells."Critical Reviews in Immunology. 18. 221-235 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Masaki Hikida: "Expression of recombination activating genes in germinal center B cells : involvement of interleukin 7 (IL-7) and the IL-7 receptor."Journal of Experimental Medicine. 188. 365-372 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Hitoshi Ohmori: "Selective augmenting effects of nitric oxide on antigen specific IgE responsein mice."Immunopharmacology. 46. 55-63 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] 大森斉: "肺中心B細胞におけるレセプターeditingとその意義"Molecular Medicine. 36. 20-28 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] 大森斉: "胚中心における抗体遺伝子再構成とその生理的意義"感染・炎症・免疫. 30. 64-66 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Masaki Hikida: "Rerrangement of λ light chain genes in mature B cells in vitro and in vivo. Function of reexpressed recombination-activating gene (RAG) products."Journal of Experimental Medicine. Vol.187. 795-799 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Hitoshi Ohmori: "Expression and function of recombination activating genes in mature B cells."Critical Reviews in Immunology. Vol.18. 221-235 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Masaki Hikida: "Expression of recombination activating genes in germinal center B cells : involvement of interleukin 7 (IL-7) and the IL-7 receptor."Journal of Experimental Medicine. Vol.188. 365-372 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Hitoshi ohmori: "Biological role of receptor editing in germina center B cells"Molecular Medicine. Vol.36. 20-28 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Hitoshi Ohmori: "IL-4-induced class switching in an anti-trinitro-phenyl hybridoma after engagement of antigen receptors"Immunol.Letters. Vol.65. 161-166 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Hitoshi Ohmori: "physiological role for V(D)J recombination in germinal center"Infection, Inflammation and Immunity. Vol.30. 64-66 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] 大森斉: "末梢リンパ組織における抗体遺伝子の再構成一抗体遺伝子の構造はどこまで柔軟か?"細胞工学. 19巻3号. 482-487 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] 大森斉: "胚中心における抗体遺伝子再構成とその生理的意義"感染・炎症・免疫. 30巻1号. 64-66 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] Hitoshi Ohmori: "Prevention of collagen-induced arthritis in DBA/1 mice by oral administration of AZ-9,a bacterial polysaccharide"Immunopharmacology. 49巻3号. 325-333 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] 大森 斉: "肺中心におけるRAG遺伝子発現とその生理的意義"Immunology Frontier. 9巻2号. 15-21 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Hitoshi Ohmori: "Selective augmenting effects of nitric oxide on antigen-specific IgE response in mice"Immunopharmacology. 46巻1号. 55-63 (2000)

    • Related Report
      1999 Annual Research Report
  • [Publications] 大森 斉: "肺中心B細胞におけるレセプターeditingとその意義"Molecular Medicine. 36巻8号. 20-28 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Masaki Hikida: "Rerrangement of λ light chain genes in mature B cells in vitro and in vivo. Function of reexpressed recombination-activating gene(RAG) products." Journal of Experimental Medicine. 1877・5. 795-799 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] Hitoshi Ohmori: "Expression and function of recombination activating genes in mature B cells." Critical Reviews in Immunology. 18・3. 221-235 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] Masaki Hikida: "Expression of recombination activating genes in germinal center B cells: involvement of interleukin 7 (IL-7) and the IL-7 receptor." Journal of Experimental Medicine. 188・2. 365-372 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] 疋田正喜: "成熟B細胞における免疫グロブリン遺伝子再構成" Annual Review免疫. 14-20 (1999)

    • Related Report
      1998 Annual Research Report

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Published: 1998-04-01   Modified: 2016-04-21  

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