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Extrathymic T cell differentiation and role of hepatic sinusoids

Research Project

Project/Area Number 02807056
Research Category

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

Allocation TypeSingle-year Grants
Research Field Immunology
Research InstitutionNiigata University School of Medicine (1991)
Tohoku University (1990)

Principal Investigator

ABO Toru  Niigata University School of Medicine, Department of Medical Zoology, Professor, 医学部, 教授 (30005079)

Co-Investigator(Kenkyū-buntansha) MASUDA Takayuki  Tohoku University School of Medicine, Second Department of Pathology Assistant p, 医学部, 助教授 (00113910)
Project Period (FY) 1990 – 1991
Project Status Completed (Fiscal Year 1991)
Budget Amount *help
¥1,500,000 (Direct Cost: ¥1,500,000)
Fiscal Year 1991: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1990: ¥1,000,000 (Direct Cost: ¥1,000,000)
Keywordsextrathymic T cells / hepatic sinusoids / intermediate TCR / alpha beta T cells / tumor immunity / NK cells / Tリンパ球 / 胸腺外分化 / 肝類洞 / αβT細胞 / γδT細胞 / intermediate TcR / ヌ-ドマウス / 胸腺摘出
Research Abstract

There exists a considerable number of unique T lymphocytes in the periphery in congenitally athymic nude mice, and in aged humans and animals with the in-voluted thymus. It is, therefore, suggested by several investigators that the extrathymic pathway of T cell differentiation may be present somewhere. We have recently demonstrated that such extrathymic T cell differentiation occurs in the hepatic sinusoids in humans and mice. This pathway of T cell differentiation resides phylogenetically earlier than the intrathymic pathway of T cell differentiation. Before and after thymic development, extrathymic T cells might work as the surveillance system for atypical cells generated in vivo by virtue of their autoreactivity. Extrathymic T cells have alpha beta TCR (and gamma delta TCR) of intermediate intensity and contain many auto-reactive T cell clones. The existence of the hepatic pathway could clearly explain the phenomenon "breakdown of self-tolerance", and occupies an important position of the immunology for aging, autoimmune disease, malignancy, bacterial infection, transplantation and allergy (immediate hypersensitivity).

Report

(3 results)
  • 1991 Annual Research Report   Final Research Report Summary
  • 1990 Annual Research Report
  • Research Products

    (23 results)

All Other

All Publications (23 results)

  • [Publications] T.Abo,et al.: "Induction of human TcRγδ+and TcR γδ-CD2+CD3-double negative lymphocytes by bacterial stimuation." Int.Immunol.2. 775-785 (1990)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] T.Ohteki,et al.: "Liver is a possible site for the proliferation of abonormal CD3+4-8-double-negative lymphocytes in autoimmune MRL-lpr/lpr mice mice." J.Exp.Med.172. 7-12 (1990)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] S.Seki,et al.: "Identification of activated T cell recepter γδ lymphocytes in the liver of tumor-bearing hosts." J.Clin.Invest.86. 409-415 (1990)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] T.Ohteki,et al.: "Predominant appearance of γδT lymphocytes in the liver of mice after birth." Eur.J.Immunol.21. 1733-1740 (1991)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] T.Abo,et al.: "The appearance of T cells bearing self-reactive T cell receptor in the livers of mice injected with bacteria." J.Exp.Med.174. 417-424 (1991)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] S.Seki,et al.: "Unusual αβ-T cells expanded in autoimmune lpr mice are probably a counterpart of normal T cells in the liver." J.Immunol.147. 1214-1221 (1991)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] T. Abo, et al.: "Induction of human TcR gamma delta + nd TcR gamma delta -CD2+CD3- double negative lymphocytes by bacterial stimulation." Int. Immunol.2. 775-785 (1990)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] T. Ohteki, et al.: "Liver is a possible site for the proliferation of abnormal CD3+4-8-double-negative lymphocytes in auto-immune MRL-1pr/1pr mice." J. Exp. Med.172. 7-12 (1990)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] S. Seki, et al.: "Identification of activated T cell receptor gamma delta lymphocytes in the liver of tumor-bearing hosts." J. Clin. Invest.86. 409-415 (1990)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] T. Ohteki, et al.: "Predominant appearance of gamma delta T lymphocytes in the liver of mice after birth." Eur. J. Immunol.21. 1733-1740 (1991)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] T. Abo, et al.: "The appearance of T cells bearing self-reactive T cell receptor in the livers of mice injected with bacteria." J. Exp. Med.174. 417-424 (1991)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] S. Seki, et al.: "Unusual alpha beta-T cells expanded in autoimmune 1pr mice are probably a counterpart of normal T cells in the liver." J. Immunol.147. 1214-1221 (1991)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] T.Abe,et al.: "Induction of human TcRγ δ+and TcR γ δ-CD2+CD3-double negative lymphocytes by bacterial stimuation." Int.Immunol.2. 775-785 (1990)

    • Related Report
      1991 Annual Research Report
  • [Publications] T.Ohteki,et al.: "Liver is a possible site for the proliferation of abonormal CD3+4-8- duobleーnegative lymphocytes in autoimmune MRLーlpr/lpr mice." J.Exp.Med.172. 7-12 (1990)

    • Related Report
      1991 Annual Research Report
  • [Publications] S.Seki,et al.: "Identification of activated T cell receptor γ δ lymphocytes in the liver of tumorーbearing hosts." J.Clin.Invest.86. 409-415 (1990)

    • Related Report
      1991 Annual Research Report
  • [Publications] T.Ohteki,er al.: "Predominant appearance of γ δ T lymphocytes in the liver of mice after birth." Eur.J.Immunol.21. 1733-1740 (1991)

    • Related Report
      1991 Annual Research Report
  • [Publications] T.Abe,et al.: "The appearance of T cells bearing selfーreactive T cell receptor in the livers of mice injected with bacteria." J.Exp.Med.174. 417-424 (1991)

    • Related Report
      1991 Annual Research Report
  • [Publications] S.Saki,et al.: "Unusual α βーT cells expanded in autoimmune lpr mice are probably a counterpart of normal T cells in the liver." J.Immunol.147. 1214-1221 (1991)

    • Related Report
      1991 Annual Research Report
  • [Publications] 安保 徹: "Liver is a possible site for the proliferation of abnomal CD3^+4^ー8^ー doubleーnegative lymphocytes in autoimmue MRLー1pr/1pr" J.Exp.Med.172. 7-12 (1990)

    • Related Report
      1990 Annual Research Report
  • [Publications] 安保 徹: "Identification of activation T cell receptor γδ lymphocytes in the liver of tumorーbearing hosts" J.Clin.Invest.86. 409-415 (1990)

    • Related Report
      1990 Annual Research Report
  • [Publications] 安保 徹: "Induction of human TCR γδ^+ and TcR γδ^ーCD2^+CD3^ー double negative lymphocytes by bacterial stimulation" Int.Immunol.2. 775-785 (1990)

    • Related Report
      1990 Annual Research Report
  • [Publications] 安保 徹: "An appropriate in vitro culture condition for the induction of human TcRγδ^+ cells by heatーkilled bacteria" J.Immunol.Methods.(1991)

    • Related Report
      1990 Annual Research Report
  • [Publications] 安保 徹: "Generation of forbidden T cell oligoclones in the liver of mice infected with bacteria" J.Exp.Med.(1991)

    • Related Report
      1990 Annual Research Report

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Published: 1990-04-01   Modified: 2016-04-21  

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