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1994 Fiscal Year Final Research Report Summary

Studies on the Immunopathogenesis of Viral Hepatitis C

Research Project

Project/Area Number 04454241
Research Category

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

Allocation TypeSingle-year Grants
Research Field Gastroenterology
Research InstitutionJichi Medical School (1993-1994)
The University of Tokyo (1992)

Principal Investigator

IMAWARI Michio  Jichi Medical School, Medicine, Professor, 医学部, 教授 (70134228)

Co-Investigator(Kenkyū-buntansha) KANEKO Takashi  Jichi Medical School, Medicine, Associate, 医学部, 助手 (10254913)
MORIYAMA Takashi  Jichi Medical School, Medicine, Assistant professor, 医学部, 講師 (10240706)
Project Period (FY) 1992 – 1994
Keywordshepatitis C virus / cytotoxic T cell / HLA B44 / antigen epitope / helper T cell
Research Abstract

We studied on T-cell responses to hepatitis C virus (HCV) nucleoprotein in patients with chronic hepatitis C to clarify the immunopathogenic mechanisms of HCV infection. We demonstrated the presence of cytotoxic T lymphocytes (CTLs) in peripheral blood of patients with HCV infection. We successfully induced HLA B44-restricted HCV-specific CTLs and defined the minimal optimal epitope to be HCV nucleoprotein residues 88 to 96. We further demonstrated that HCV-specific helper T cells existed and stimulated activation and proliferation of CTLs. HCV mutates rapidly. but is classified into several genotypes. An amino acid sequence of HCV nucleoprotein residues 88 to 96 is conserved among HCV isolates except for residue 91. An amino acid at residue 91 is also conserved among the members of the same genotype of HCV.HLA B44-restricted HCV-specific CTLs could be induced by and recognized HCV of genotypes II/1b and III/2a, but neither I/1a nor IV/2b. A rare variant HCV of genotype I/1a, however, could induced HLA B44-restricted HCV-specific CTLs. The results contribute not only to elucidationof the immunopathogenic mechanisms of HCV infection but also to designing CTL vaccines to prevent HCV infection and eliminate HCV from infected patients with HLA B44.

  • Research Products

    (8 results)

All Other

All Publications (8 results)

  • [Publications] 森山貴志: "トランスジェニックマウスを用いた肝障害発症機序の研究" 実験医学. 10. 139-169 (1992)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 森山貴志: "慢性肝炎の発症機序と対策" Practitioners. 2. 163-169 (1993)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 井廻道夫: "ウイルス性疾患の細胞障害機序とその対策" Medical Practice. 10. 858-863 (1993)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Kita,Hiroto: "HLA B44-restricted cytotoxic T lymphocytes recognizing an epitope on hepatitis C virus nucleocapsid protein" Hepatology. 18. 1039-1044 (1993)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 井廻道夫: "C型肝炎の細胞性免疫応答" 最新医学. 49. 301-303 (1994)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Hiroto,Kita: "A helper T-cell antigen enhances generation of hepatitis C virus-specific cytotoxic T lymphocytes in vitro" Journal of Medical Virology. (発表予定). (1995)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Kita, Hiroto et al.: "HLA B44-restricted cytotoxic T lymphocytes recognizing an epitope on hepatitis C virus nucleocapsid protein." Hepatology. 18. 1039-1044 (1993)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Kita, Hiroto et al.: "A helper T-cell antigen enhances generation of hepatits C virus-specific cytotoxic T lymphocytes in vivo" J Med Virol. (in press). (1995)

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

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Published: 1996-04-15   Modified: 2021-10-15  

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