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An analysis for mechanism of antitumor effects of dendritic cells treated with αGalactosylceramide

Research Project

Project/Area Number 13672079
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Surgical dentistry
Research InstitutionTOHOKU UNIVERSITY

Principal Investigator

HASHIMOTO Wataru  Dental Hospital, Assistant Professor, 歯学部附属病院, 助手 (30323033)

Project Period (FY) 2001 – 2002
Project Status Completed (Fiscal Year 2002)
Budget Amount *help
¥3,600,000 (Direct Cost: ¥3,600,000)
Fiscal Year 2002: ¥1,800,000 (Direct Cost: ¥1,800,000)
Fiscal Year 2001: ¥1,800,000 (Direct Cost: ¥1,800,000)
Keywordsgalactosylceramide / antitumor effects / NKT cells / IFN-γ / IL-12 / dendritic cells / Intratumoral injection / tumor immunotherapy
Research Abstract

We have already reported that intratumoral injection of dendritic cells (DCs) treated with αGalactosylceramide (αGalCer) selectively activated natural killer T cells (NKT cells), resulting in regression of day 7 established poorly immunogenic tumors.
To clarify a role of IL-12 produced by DCs, α-GalCer treated-DCs harvested from IL-12 deficient mice can inhibits MCA205 tumor growth as strong as using WT's DCs. Interestingly, α-GalCer injection can not enhance the in vitro cytotoxicity of lymphocytes harvested from IFN-γ-deficient mice. Furthermore, the antitumor activity of using DCs treated with α-GalCer in IFN-γ-deficient mice is impaired comopletely. These results indicate that IFN-γ, but IL-12, plays critical role in these antitumor response of α-GalCer treated-DCs.
Next, we investigated the antitumor effects of αGalCer on human peripheral blood mononuclear cells (PBMC). Phenotypic analysis revealed an expansion of CD3+ CD161+ CD56- Vα24TCR+ T cells on PBMC. These results are consistent with the previous reports showing that α-GalCer selectively activates Vα14NKT cells in mice, suggesting that intratumoral injection of α-GalCer treated-DC should be considered a viable strategy for the generation of antitumor responses on human and for further clinical applications for head and neck tumors.

Report

(3 results)
  • 2002 Annual Research Report   Final Research Report Summary
  • 2001 Annual Research Report
  • Research Products

    (15 results)

All Other

All Publications (15 results)

  • [Publications] 橋元 亘: "樹状細胞の腫瘍内投与"血液・腫瘍科. 45. 44-48 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] T.Kobayashi, W.Hashimoto 他5名: "Interleukin-12 administration is more effective for preventing metastases than for inhibiting primary established tumors in a murine model of spontaneous hepatic metastases"Surg. Today. 32. 236-242 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] F.Tanaka, W.Hashimoto 他3名: "Therapeutic and specimunity induced by co-administration of immature dendritic cells and adenoviral vector expressing biologically active IL-18"Gene Therapy. 21. 1480-1486 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] W.Hashimoto 他6名: "NK but not NKT cells play a necessary role to promote an innate antitumor response induced by IL-18"Int. J. Cancer. 103. 508-513 (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] 橋元 亘 他3名: "Interleukin-18によるNatural Killer(NK)細胞活性化および腫瘍細胞のアポトーシス誘導"頭頸部腫瘍. 29. 1-7 (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] W.Hasfaimoto: "Intratumcral injection of dendritic cells"Hematology & Oncology. 45. 44-48 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] T.Kobayashi, K.Shiiba, M.Satoh, W.Hashimoto, T.Mizoi, S.Matsuno, K.Takeda: "Interleukin 12 administration is more effective for preventing metastases than for inhibiting primary established tumors in a murine model of spontaneous hepatic metastases"Surg. Today. 32. 236-242 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] R.Tanaka, W.Hashimoto, P.D.Robbins, M.T,Lotze, H.Tahara: "Therapeutic and specific antitumor immunity induced by co-administration of immature dendritic cells and adenoviral vector expressing biologically active IL-18"Gene Therapy. 21. 1480-1486 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] W.Hashimoto, E.Tanaka, R.D.Robbins, M.Taniguchi, H.Okamura, M.T.Lotze, H.Tahara: "NK but not NKT cells play a necessary role to promote an innate antitumor response induced by IL-18"Int. J. Cancer. 103. 508-513 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] W.Hashimoto, F.Shinohara, M.Takahashi, S.Echigo: "Interleukin-18 (IL-18) activates natural killer cells and induces turner apoptosis"Head and Neck Cancer. 29. 217-223 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] 橋元 亘: "樹状細胞の腫瘍内投与"血液・腫瘍科. 45. 44-48 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] T.Kobayashi, W.Hashimoto他5名: "Interleukin-12 administration is more effective for preventing metastases than for inhibiting primary established tumors in a murine model of spontaneous hepatic metastases"Surg.Today. 32. 236-242 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] F.Tanaka, W.Hashimoto他3名: "Therapeutic and specimunity induced by co-administration of immature dendritic cells and adenoviral vector expressing biologically active IL-18"Gene Therapy. 21. 1480-1486 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] W.Hashimoto他6名: "NK but not NKT cells play a necessary role to promote an innate antitumor response induced by IL-18"Int.J.Cancer. 103. 508-513 (2003)

    • Related Report
      2002 Annual Research Report
  • [Publications] 橋元 亘他3名: "Interleukin-18によるNatural Killer(NK)細胞活性化および腫瘍細胞のアポトーシス誘導"頭頸部腫瘍. 29. 1-7 (2003)

    • Related Report
      2002 Annual Research Report

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Published: 2001-04-01   Modified: 2016-04-21  

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