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2009 Fiscal Year Final Research Report

Senescence and maintenance mechanism of antigen-specific CD8+ T cells upon repeatitive antigenic challenges.

Research Project

  • PDF
Project/Area Number 20790369
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeSingle-year Grants
Research Field Immunology
Research InstitutionThe University of Tokyo

Principal Investigator

KURACHI Makoto  The University of Tokyo, 大学院・医学系研究科, 助教 (00396722)

Project Period (FY) 2008 – 2009
Keywords免疫記憶 / 老化 / CD8陽性T細胞 / 二次リンパ組織
Research Abstract

Although it is suggested that the nature of memory CTL changes over repeated antigenic challenges, molecular characteristics of distinct memory CTL with different number of antigen experience are largely unknown. In this study, we analyzed genome wide transcriptome of primary and secondary memory CTL using a next-generation DNA sequencer. Memory CTL changes molecular signature as they experience the responses and memory CTL senescence differs from exhaustion.

  • Research Products

    (4 results)

All 2010 2009 2008 Other

All Journal Article (1 results) (of which Peer Reviewed: 1 results) Presentation (2 results) Remarks (1 results)

  • [Journal Article] Bone marrow graft-versus-host disease: early destruction of hematopoietic niche following MHC-mismatched hematopoietic stem cell transplantation.2010

    • Author(s)
      Shono Y, Kurachi M, et al
    • Journal Title

      Blood (In press)

    • Peer Reviewed
  • [Presentation] メモリーCTLの老化に伴う遺伝子発現解析2009

    • Author(s)
      倉知慎, 他
    • Organizer
      第39回日本免疫学会総会・学術総会
    • Place of Presentation
      大阪(グランキューブ大阪)
    • Year and Date
      2009-12-03
  • [Presentation] Primary memory CTL preferentially accumulate in secondary lymphoid organs2008

    • Author(s)
      倉知慎, 他
    • Organizer
      第38回日本免疫学会総会・学術総会
    • Place of Presentation
      京都(国立京都国際会館)
    • Year and Date
      2008-12-02
  • [Remarks]

    • URL

      http://www.prevent.m.u-tokyo.ac.jp/

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Published: 2011-06-18   Modified: 2016-04-21  

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