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Perticipation of IgE level reguratory gene on protection to helminth infections.

Research Project

Project/Area Number 06670273
Research Category

Grant-in-Aid for General Scientific Research (C)

Allocation TypeSingle-year Grants
Research Field 寄生虫学(含医用動物学)
Research InstitutionJikei University School of Medicine

Principal Investigator

WATANABE Naohiro  Jikei University School of Medicine Department of Tropical Medicine, Associate Professor, 医学部, 助教授 (00057019)

Project Period (FY) 1994 – 1995
Project Status Completed (Fiscal Year 1995)
Budget Amount *help
¥2,100,000 (Direct Cost: ¥2,100,000)
Fiscal Year 1995: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 1994: ¥1,200,000 (Direct Cost: ¥1,200,000)
KeywordsIgE / Genetic regulation / Parasite / Protective immunity / Helminth / Hymenolepis / Trichinella / Atopy
Research Abstract

The aim of study is to know the role of IgE in host defense to helminth infection. The study focused on the effect of IgE-level regulatory gene on the protection to helminth infection in mice. It has been demonstrated by myself that this gene regulates IgE production, restricted for IgE isotype and not restricted to antigens stimulated. this gene is considered to be equivalent to an atopy gene in humans. The strains of mice were divided into high and low responders under the regulation of this gene. the experiments were performed to determine IgE dependency of protection to helminths comparing between selective IgE-deficient and IgE-producing control mice of high or low IgE responder strains. Anti-helminth IgE antibody had protective roles in expulsion of Hymenolepis nana, resistance to Trichinella spiralis. IgE antibody dependency of protective immunity to Trichinellaspiralis was found only in the host expressing high IgE phenotype but not in low IgE phenotype. To clarify the effect of IgE-level regulatory gene on defense function to Trichinella spiralis, backcross (N2 generation) mice of high and low responders were infected with Trichinella spiralis. The half of N2 mice were high IgE responders and the other half were low responders, confirming my previous finding of one gene. IgE responsiveness in each of N2 mice was inversely correlated to the protective function to Trichinella spiralis. This result suggests that IgE-level regulatory gene regulates defense function to helminth as an IgE-dependent protection gene. Therefore, it would be likely that the fundamental role of IgE is protection to helminths.

Report

(3 results)
  • 1995 Annual Research Report   Final Research Report Summary
  • 1994 Annual Research Report
  • Research Products

    (12 results)

All Other

All Publications (12 results)

  • [Publications] Watanabe,N.: "Expulsion of Hymenolepis nana from mice with congenital deficiencies of IgE production or of mast cell development." Parasite Immunol.16. 137-144 (1994)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Saito,S.: "Preferential insduction of IL-4 is determined by the type and duration of antigenic stimulation." Cell. Immunol.153. 1-8 (1994)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Watanabe,N.: "Brugia malayi infection in mice with selective suppression of IgE production." Int. Arch. Allergy Immunol.109. 192-196 (1996)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Korenaga,M.: "Acceleration of IgE responses by treatment of rIL-3 prior to infection with Trichinella spiralis in mice." Immunol.(in press). (1996)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Watanabe, N., et al.: "Expulsion of Hymenolepis nana from mice with congenital deficiencies of IgE production or of mast cell development." Parasite Immunol.16. 137-144 (1994)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Saito, S., et al.: "Preferential induction of IL-4 is determined by the type and duration of antigenic stimulation." Cell.Immun.153. 1-8 (1994)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Watanabe, N., et al.: "Brugia malayi infection in mice with selective suppression of IgE production." Int.Arch.Allergy Immumol.109. 192-196 (1996)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Korenaga, M., et al.: "Acceleration of IgE responses by treatment of rIL-3 prior to infection with Trichinella spiralis in mice." Immunol.(in press). (1996)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Watanabe, N.: "Brugia malayi infection in mice with selective suppression of IgE production." Int. Arch. Allergy Immunol.109. 192-196 (1996)

    • Related Report
      1995 Annual Research Report
  • [Publications] Korenaga, M.: "Acceleration of IgE responses by treatment of rIL-3 prior to infection with Trichinella spiralis in mice." Immunol.(in press). (1996)

    • Related Report
      1995 Annual Research Report
  • [Publications] Watanabe,N.: "Expulsion od Hymenolepis nana from mice with corgenital deficiencies of IgE production or of mast cell development." Parasite Immunology. 16. 137-144 (1994)

    • Related Report
      1994 Annual Research Report
  • [Publications] Saito,S.: "Preferential induction of IL-4 is determined by the type and duration of antigemic stimulation." Cellular Immunology. 153. 1-8 (1994)

    • Related Report
      1994 Annual Research Report

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Published: 1994-04-01   Modified: 2016-04-21  

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