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New therapeutic vaccines by using small membrane vesicle secreted by dendritic cells: New development for chronic virus infections

Research Project

Project/Area Number 22591111
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Infectious disease medicine
Research InstitutionSaitama Medical University

Principal Investigator

MORIYA Osamu  埼玉医科大学, 医学部, 准教授 (40049862)

Co-Investigator(Renkei-kenkyūsha) KOBAYASHI Nobuharu  埼玉医科大学, 医学部, 講師 (10150616)
Project Period (FY) 2010 – 2012
Project Status Completed (Fiscal Year 2012)
Budget Amount *help
¥4,420,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥1,020,000)
Fiscal Year 2012: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2011: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2010: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Keywords感染症治療学 / 慢性ウイルス感染 / エキソソーム / 樹状細胞 / CTL / 刺激因子 / NK細胞 / 細胞傷害性T細胞 / HHDマウス / 慢性ウイルス感染症 / IFNγ産生細胞 / HHDトランスジェニックマウス
Research Abstract

In this study, we investigated whether exosome (Ex) derived from dendritic cells (DC) can be attractive candidate for antiviral immunity in the transgenic mice (HHD) expressing HLA-A0201. We isolated Ex from culture supernatant of DC that were infected with recombinant Adenovirus (Rec Ad) expressing NS3-5A of Hepatitis C virus (HCV) with or without maturation reagents of DC such as LPS, IL-12, CpG, phorbor ester, ionomycin, CD40L or ATP. By estimating dot blot assay, Ex contained CD63, CD81, CD44, I-Ab, HLA-A2, HSP, and Raeδ. Responses of cytotoxic T lymphocytes (CTL) or natural killer cells were induced by these Exs. IFN γsyntheses estimated by ELISPOT assay showed increased numbers of secreting cells. From the findings of increased concentration of Raeδand HSP in Exs and the frequency of NKG2D-positive cells in the splenic cells after the Ex stimulation, we hypothesized that NK cell increases in number induce IFN γ synthesis and cytolytic function in part just after the Ex stimulation. CD8+ T cells, but not CD4+ T cells may be important for the effects of Ex on CTL responses. Among the TLRs tested, TLR-2 suggested an important role as receptor of Ex in addition to the well known LFA molecules.

Report

(4 results)
  • 2012 Annual Research Report   Final Research Report ( PDF )
  • 2011 Annual Research Report
  • 2010 Annual Research Report
  • Research Products

    (4 results)

All 2012 2011 Other

All Presentation (4 results)

  • [Presentation] Exosomes derived from dendritic cells treated with CpG ODN stimulated cytolytic responses and induction of memory cells in anti-viral immune responses2012

    • Author(s)
      Moriya Osamu
    • Organizer
      第41回日本免疫学会総会・学術総会
    • Place of Presentation
      神戸市国際会議場
    • Year and Date
      2012-12-06
    • Related Report
      2012 Final Research Report
  • [Presentation] Akatsuka Toshitaka. Exosomes released from dendritic cells are immunomodulator in viral infection2011

    • Author(s)
      Moriya Osamu
    • Organizer
      第40回日本免疫学会総会・学術総会
    • Place of Presentation
      千葉市幕張メッセ
    • Year and Date
      2011-11-28
    • Related Report
      2012 Final Research Report
  • [Presentation] Exosomes released from dendritic cells are immunomodulator in viral infection2011

    • Author(s)
      守屋修、赤塚俊隆
    • Organizer
      日本免疫学会
    • Place of Presentation
      千葉市幕張メッセ
    • Year and Date
      2011-11-28
    • Related Report
      2011 Annual Research Report
  • [Presentation] Exosomes derived from dendritic cells treated with CpG ODN stimulate cytolytic responses and induction of memory cells in antiviral immune responses

    • Author(s)
      守屋修
    • Organizer
      日本免疫学会
    • Place of Presentation
      神戸国際会議場(兵庫県)
    • Related Report
      2012 Annual Research Report

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Published: 2010-08-23   Modified: 2019-07-29  

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