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HPV 16-associated tumours: IL-12 can repair the absence of cytotoxic and proliferative responses of tumour infiltrating cells after chemotherapy

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    SYSNO ASEP0318305
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleHPV 16-associated tumours: IL-12 can repair the absence of cytotoxic and proliferative responses of tumour infiltrating cells after chemotherapy
    TitleHPV 16-asociované nádory: IL-12 může obnovit cytotoxické a proliferační odpovědi buněk infiltrujících nádor po chemoterapii
    Author(s) Indrová, Marie (UMG-J) RID
    Bieblová, Jana (UMG-J)
    Rossowska, J. (PL)
    Kuropka, P. (PL)
    Pajtasz-Piasecka, E. (PL)
    Bubeník, Jan (UMG-J)
    Reiniš, Milan (UMG-J) RID
    Source TitleInternational Journal of Oncology. - : Spandidos Publications - ISSN 1019-6439
    Roč. 34, č. 1 (2009), s. 173-180
    Number of pages8 s.
    Languageeng - English
    CountryGR - Greece
    KeywordsHPV 16 ; vaccines ; tumour-infiltrating cells
    Subject RIVEB - Genetics ; Molecular Biology
    R&D ProjectsGA301/06/0774 GA ČR - Czech Science Foundation (CSF)
    CEZAV0Z50520514 - UMG-J (2005-2011)
    UT WOS000262127000017
    AnnotationWe have examined the effect of IL-12-producing cellular vaccines on the cytotoxicity and proliferative potential of CD45+ tumour-infiltrating cells (TIL) in mice carrying syngeneic, HPV 16-associated tumours after chemotherapy with CBM-4A ifosfamide derivative. The chemotherapy resulted in decrease of the CD4+ and CD8+ TIL, increase of the Gr-1+/CD11b+ TIL, no changes in the infiltration with CD4+/CD25+ Treg TIL, and decrease of the cytolytic and proliferative potential of the CD45+ TIL. Subsequent immunotherapy with the IL-12-producing, genetically modified TC-1 cells increased tumour infiltration with CD8+ and CD4+ cells, decreased the Gr-1+/CD11b+ cells, and increased the cytolytic and proliferative potential of the CD45+ TIL. These findings suggest that peritumoral administration of the IL-12-producing cellular vaccine can restore the cytolytic potential and inhibit immunosuppressive TIL-dependent mechanisms.
    WorkplaceInstitute of Molecular Genetics
    ContactNikol Škňouřilová, nikol.sknourilova@img.cas.cz, Tel.: 241 063 217
    Year of Publishing2009
Number of the records: 1  

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