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Immuno-gene Therapy of Cancer by Interleukin-21 (IL-21)

Research Project

Project/Area Number 14571151
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field General surgery
Research InstitutionKyoto Prefectural University of Medicine

Principal Investigator

IMANISHI Jiro  Kyoto Prefectural University of Medicine, Graduate School of Medicine, Associate Professor, 医学研究科, 教授 (40112510)

Co-Investigator(Kenkyū-buntansha) MAZDA Osam  Kyoto Prefectural University of Medicine, Graduate School of Medicine, Associate Professor, 医学研究科, 助教授 (00271164)
Project Period (FY) 2002 – 2003
Project Status Completed (Fiscal Year 2003)
Budget Amount *help
¥2,800,000 (Direct Cost: ¥2,800,000)
Fiscal Year 2003: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 2002: ¥2,000,000 (Direct Cost: ¥2,000,000)
KeywordsIL-21 / IL-15 / Liver metastatis. / CTL / NK / immunotherapy / Intravascular gene delivery / Naked plasmid DNA / 腫瘍免疫 / NK細胞
Research Abstract

Interleukin-21 (IL-21) is secreted from activated CD4+ T cells, supporting mature T and B lymphocyte proliferation. The cytokine synergizes with IL-15 to promotes expansion and maturation of natural killer (NK) cells. These immunomodulatory functions of IL-21 have been revealed by in vitro studies ; however, the biological implications of IL-21 in vivo have not been fully elucidated. Here, we performed intravascular transfection of IL-21 and/or IL-15 in an experimental murine model of metastatic liver tumors. IL-21 and IL-15 expression plasmids were intravenously injected under high pressure into the tail veins of mice, which were subsequently challenged by an intravenous injection of RLmale1 lymphoma cells. Although the mock-treated and IL-21-transfected mice developed metastatic lymphomas in the liver, IL-15 gene transfection significantly reduced the numbers of metastatic tumor foci. In contrast, when IL-21 and IL-15 genes were co-transfected, complete regression was achieved in 80% of the mice. The cytokine gene therapy was also performed in mice that had been intravenously inoculated with the tumor, cells. Forty percent of mice that received a single injection of a mixture of cytokine genes successfully rejected the pre-established metastatic lymphoma, and showed tumor-free survival for more than 300 days. IL-21 significantly elevated the cytotoxic T lymphocyte (CTL) activity in the spleens of tumor-inoculated mice, while the two cytokines augmented natural killer (NK) killing activity in a synergistic manner. Serum concentrations of interferon-gamma (IFN-gamma), IL-4, and GM-CSF were not significantly affected by the cytokine treatment. These results strongly suggest that the co-administration of genes encoding IL-21 and IL-15 induces powerful antitumor immune responses without causing any severe inflammatory adverse effects, resulting in drastic therapeutic efficacy against metastatic malignancies.

Report

(3 results)
  • 2003 Annual Research Report   Final Research Report Summary
  • 2002 Annual Research Report
  • Research Products

    (22 results)

All Other

All Publications (22 results)

  • [Publications] Kishida, T. et al.: "Interleukin (IL)-21 and IL-15 Genetic Transfer Synergistically Augments Therapeutic Antitumor Immunity and Promotes Regression of Metastatic"Mol.Ther.. 8・4. 552-558 (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Kishida, T. et al.: "Electrochemo-gene-tnerapy or Cancer : Intratumorat Delivery or InterleuKin-Geneand Bleomycin Synergistically Induced Therapeutic Immunity and Suppressed Subcutaneous and Metastatic Melanomas in Mice"Mol.Ther.. 6・1. 105-110 (2004)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Itokawa Y. et al.: "IL-12 genetic administration suppressed metastatic liver tumor unsusceptible to CTL"Biochem.Biophys.Res.Commun.. 314・4. 1072-1079 (2004)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Nakanishi, H. et al.: "Nonviral genetic transfer of Fas ligand induced significant growth suppression and apoptotic tumor cell death in prostate cancer in vivo."Gene Ther.. 10・5. 434-442 (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Asada, H. et al.: "Significant Antitumor Effects Obtained by Autologous Tumor Cell Vaccine Engineer-ed to Secrete Interleukin (IL)- 12 and 11-18 by Means of the EBV/Lipoplex."Mol.Ther.. 5・5. 609-616 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Kishia T. et al.: "Interleukin (IL)-21 and IL-15 Genetic Transfer Synergistically Augments Therapeutic Antitumor Immunity and Promotes Regression of Metastatic Lymphoma"Mol.Ther.. 8(4). 552-558 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Kishida, T. et al.: "Electrochemo-gene-therapy of Cancer : Intratumoral Delivery of Interleukin-12 Gene and Bleomycin Synergistically Induced Therapeutic Immunity and Suppressed Subcutaneous and Metastatic Melanomas in Mice"Mol.Ther.. 6(1). 105-110 (2004)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Itokawa Y. et al.: "IL-12 genetic administration suppressed metastatic liver tumor unsusceptible to CTL"Biochem.Biophys.Res.Commun.. 314(4). 1072-1079 (2004)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Nakanishi, H. et al.: "Nonviral genetic transfer of Fas ligand induced significant growth suppression and apoptotic tumor cell death in prostate cancer in vivo."Gene Ther.. 10(5). 434-442 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Asada, H. et al.: "Significant Antitumor Effects Obtained by Autologous Tumor Cell Vaccine Engineer-ed to Secrete Interleukin (IL)-12 and LL-18 by Means of the EBV/Lipoplex."Mol.Ther.. 5(5). 609-616 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Kishida, T. et al.: "Interleukin (IL)-21 and IL-15 Genetic Transfer Synergistically Augments Therapeutic Antitumor Immunity and Promotes Regression of Metastatic Lymphoma"Mol.Ther.. 8・4. 552-558 (2003)

    • Related Report
      2003 Annual Research Report
  • [Publications] Kishida, T. et al.: "Electrochemo-gene-therapy of Cancer : Intratumoral Delivery of Interleukin-12 Gene and Bleomycin Synergistically Induced Therapeutic Immunity and Suppressed Subcutaneous and Metastatic Melanomas in Mice"Mol.Ther.. 6・1. 105-110 (2004)

    • Related Report
      2003 Annual Research Report
  • [Publications] Itokawa Y. et al.: "IL-12 genetic administration suppressed metastatic liver tumor unsusceptible to CTL"Biochem.Biophys.Res.Commun.. 314・4. 1072-1079 (2004)

    • Related Report
      2003 Annual Research Report
  • [Publications] Nakanishi, H. et al.: "Nonviral genetic transfer of Fas ligand induced significant growth suppression and apoptotic tumor cell death in prostate cancer in vivo."Gene Ther.. 10・5. 434-442 (2003)

    • Related Report
      2003 Annual Research Report
  • [Publications] Asada, H. et al.: "Significant Antitumor Effects Obtained by Autologous Tumor Cell Vaccine Engineered to Secrete Interleukin (IL)-12 and IL-18 by Means of the EBV/Lipoplex."Mol.Ther.. 5・5. 609-616 (2002)

    • Related Report
      2003 Annual Research Report
  • [Publications] Shin-Ya, M. et al.: "Interleukin-2 Abolishes Myeloid Cell Accumulation Induced by Lewis Lung Carcinoma"J.Interferon Cytokine Res.. 23・11. 631-638 (2003)

    • Related Report
      2003 Annual Research Report
  • [Publications] Iwai, M., et al.: "Suicide Gene Therapy of Human Hepatoma and Its Peritonitis Carcinomatosis by a Vector of Replicative-Deficient Herpes Simple Vinus"Biochem. Biophys. Res. Commun.. 291・4. 855-860 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] Asada, H., et al.: "Significant Antitumor Effects Obtained by Autologous Tumor Cell Vaccine Engineered to Secrete Interleukin (IL)-12 and IL-18 by Means of the EBV/Lipoplex"Mol. Ther.. 5・5. 609-616 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] Ohashi, S., et al.: "Successful Genetic Transduction in vivo into Synovium by Means of Electroporation"Biochem. Biophys. Res. Commun.. 293・5. 1530-1535 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] Hirai H., et al.: "Hemogenic and nonhemogenic endothelium can be distinguished by the activity of fetal liver kinase (Flk)-1 promoter/enhancer during mouse embryogenesis"Blood. 101・3. 886-893 (2003)

    • Related Report
      2002 Annual Research Report
  • [Publications] Nakanishi, H., et al.: "Nonviral genetic transfer of Fas ligand induced significant growth suppression and apoptotic tumor cell death in prostate cancer in vivo"Gene Ther.. 10・5. 434-442 (2003)

    • Related Report
      2002 Annual Research Report
  • [Publications] Terauchi, R., et al.: "Heat Shock Protein 70 Prevents Nitric Oxide-Induced Apoptosis in Articular Chondrocytes"Arthritis Rheumatism. (印刷中).

    • Related Report
      2002 Annual Research Report

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Published: 2002-04-01   Modified: 2016-04-21  

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