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1997 Fiscal Year Final Research Report Summary

Analysis of IgE-level regulatory gene involving protection against helminth infections.

Research Project

Project/Area Number 08670292
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
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) 1996 – 1997
KeywordsIgE / genetic control / parasite / protective immunity / helminth / linkage analysis / Trichinella / atopy
Research Abstract

The objective of this study is to identify the characteristics and gene locus of IgE-level regulatory gene which controls IgE-dependent protection against helminth parasites. We previously demonstrated that strains of mice can be classified into IgE-high and -low responders under the control of IgE-level regulatory gene. Backcross (N2) mice were obtained by breeding between high and low responders. After infection with Trichinella spiralis, IgE production in N2 mice segregated into IgE-high and low responders with the ratio of 1 : 1, confirming a single autosomal gene. The numbers of T.spiralis recovered from IgE-high N2 mice were significantly smaller than those from IgE-low N2 mice. This results suggest that IgE-level regulatory gene controls protection against T.spiralis. The linkage analysis between IgE levels in N2 mice and microsatellite markers on chromosomes is in progress. The second experiments were carried out in NC/Nga mice with hyper IgE.The trait of hyper IgE is IgE-isotype specific and antigen-nonspecific, suggesting a novel IgE-level regulatory gene. In the crossing experiments, the ratio between mice with hyper IgE and with normal were 1 : 15 in F2 generation and 1 : 3 in N2 generation. These results suggest that the hyper IgE is controlled by two autosomal genes with recessive trait. We proposed the gene symbols ieh1 and ieh2 for the genes.

  • Research Products

    (14 results)

All Other

All Publications (14 results)

  • [Publications] 渡辺 直煕: "寄生虫感染防御におけるIgE" アレルギー科. 1. 535-539 (1996)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Korenaga, M.: "Acceleration of IgE by treatment with recombinant interleukine-3 prior to infection with Trichinella spiralis in mice." Immunol.87. 642-646 (1996)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Hamada, A.: "Nerve growth factor enhances survival and cytotoxic activity of human eosinophils." Brit.J.Haematol. 93. 299-302 (1996)

    • Description
      「研究成果報告書概要(和文)」より
  • [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
  • [Publications] Matsuda, H.: "Development of atopic dermatitis with IgE hyperproduction in NC/Nga mice." Int.Immunol.9. 461-466 (1997)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Tsudzuki, M.: "Genetic analyses for dermatitis and IgE hyperproduction in the NC/Nga mouse." Immunogenetics. 47. 88-90 (1997)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Nakajima, A.: "Requirement of CD28-CD86 co-stimulation in the interaction between antigen-primed T helper type 2 and B cells." Int.Immunol.9. 637-644 (1997)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 渡辺 直煕: "IgE抗体の産生調節機構" 医学のあゆみ. 180. 3-6 (1997)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Korenaga, M.et al.: "Acceleration of IgE by treatment with recombinant interleukine-3 prior to infection with Trichinellq spiralis in mice." Immunol.87. 642-646 (1996)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Hamada, A.et al.: "Nerve growth factor enhances survival and cytotoxic activity of human eosinophils." Brit.J Heamatol.93. 299-302 (1996)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Watanabe, N.et al.: "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(欧文)」より
  • [Publications] Matsuda, H.et al.: "Development of atopic dermatitis with IgE hyperproduction in NC/Nga mice." Int.Immunol.9. 461-466 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Tsudzuki, M.et al.: "Genetic analyzes for dermatitis and IgE hyperproduction in the NC/Nga mouse." Immunogenetics.47. 88-90 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Nakajima, A.et al.: "Requirement of CD28-CD86 co-stimulation in the interaction between antigen-primed T helper type 2 and B cells" Int.Immunol.9. 637-644 (1997)

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 1999-03-16  

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