Induction of an antitumor immunological response by an intratumoral injection of dendritic cells pulsed with genetically engineered Semliki Forest virus to produce interleukin-18 combined with the systemic administration of interleukin-12
| Autor: | Ryuya Yamanaka, Hitoshi Hasegawa, Kleanthis G. Xanthopoulos, Naoto Tsuchiya, Ryuichi Tanaka, Junpei Honma, Jay Ramsey, Naoki Yajima, R. Michael Blaese |
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| Rok vydání: | 2003 |
| Předmět: |
Male
DNA Complementary medicine.medical_treatment Semliki Forest virus Mice Antigens CD Transduction Genetic Cricetinae Immunogenetics Tumor Cells Cultured medicine Animals DNA Primers biology Brain Neoplasms Reverse Transcriptase Polymerase Chain Reaction Interleukin-18 Immunotherapy Active Interleukin Dendritic Cells Genetic Therapy Glioma T-Lymphocytes Helper-Inducer Immunotherapy Dendritic cell biology.organism_classification Interleukin-12 Semliki forest virus Killer Cells Natural Mice Inbred C57BL Antibody Formation Immunology Interleukin 12 Systemic administration Interleukin 18 Genetic Engineering CD8 |
| Zdroj: | Journal of Neurosurgery. 99:746-753 |
| ISSN: | 0022-3085 |
| Popis: | Object. The aim of this study was to investigate further immunogene treatment of malignant brain tumor to improve its therapeutic efficacy. Methods. Intratumoral dendritic cells pulsed with Semliki Forest virus (SFV)—interleukin-18 (IL-18) and/or systemic IL-12 were injected into mice bearing the B16 brain tumor. To study the immune mechanisms involved in tumor regression, we monitored the growth of implanted B16 brain tumor cells in T cell—depleted mice and IFNγ-neutralized mice. To analyze the protective immunity created by tumor inoculation, B16 cells were injected into the left thighs of mice that had received an inoculation, and tumor growth was monitored. The local delivery of dendritic cells pulsed with IL-18 bound by SFV combined with the systemic administration of IL-12 enhanced the induction of the T helper type 1 response from tumor-specific CD4+ and CD8+ T cells and natural killer cells as well as antitumor immunity. Interferon-γ is partly responsible for this IL-18—mediated antitumor immunity. Furthermore, the protective immunity is mediated mainly by CD8+ T cells. Conclusions. Immunogene therapy that combines the local administration of dendritic cells pulsed with IL-18 bound by SFV and the systemic administration of IL-12 may be an excellent candidate for the development of a new treatment protocol. A self-replicating SFV system may therefore open a novel approach for the treatment of malignant brain tumor. |
| Databáze: | OpenAIRE |
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