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Comprehensive analysis of dysfunctional HCV specific CD8 T cell during persistent HCV infection

Research Project

Project/Area Number 24790720
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Gastroenterology
Research InstitutionKeio University

Principal Investigator

Ishibashi Yuka  慶應義塾大学, 医学部, 助教 (60528305)

Research Collaborator Nobuhiro Nakamoto  慶應義塾大学, 医学部(信濃町), 専任講師 (40383749)
Project Period (FY) 2012-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2015: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2014: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2013: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2012: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
KeywordsC型肝炎ウイルス / T細胞疲弊 / 獲得免疫 / C型肝炎 / CD8 T細胞 / NK細胞 / 免疫寛容 / 腸肝相関 / HCV特異的T細胞 / T細胞の疲弊 / C型慢性肝炎 / CD8T細胞 / NKT細胞 / exhaustion
Outline of Final Research Achievements

Peripheral HCV specific CD8 T cells in patients with chronic HCV infections showed higher expressions of suppressive co-stimulation molecules such as PD-1, CTLA4, and LAG-3 compared with EBV or influenza specific CD8 T cells from the same individuals. HCV specific CD8 T cells in patients with higher viral load tended to express multiple suppressive co-stimulation molecules. Of interest, PD-1 positive HCV specific CD8 T cells produced higher TNFα and lower IL-10 compared with PD-1 negative subsets. There results suggest that HCV specific CD 8 T cells fall to be dysfunctional via the expression of multiple suppressive co-stimulation molecules during persistent HCV infection. Further study is needed to clarify the mechanism behind the immune tolerance in the liver and to overcome the HCV infection in humans.

Report

(5 results)
  • 2015 Annual Research Report   Final Research Report ( PDF )
  • 2014 Research-status Report
  • 2013 Research-status Report
  • 2012 Research-status Report
  • Research Products

    (1 results)

All Other

All Presentation (1 results)

  • [Presentation] C型慢性肝炎難治例における抗ウイルス療法中の末梢血HCV特異的CD8 T細胞機能の経時的変化と補助シグナル阻害による機能修飾の検討

    • Author(s)
      中本伸宏
    • Organizer
      第17回日本肝臓学会大会
    • Place of Presentation
      東京
    • Related Report
      2013 Research-status Report

URL: 

Published: 2013-05-31   Modified: 2019-07-29  

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