Effects of immunotherapy of IL-6 and IL-15 plasmids on transmissible venereal tumor in beagles
Canine transmissible venereal tumor (CTVT) is a tumor with low MHC antigen expression and is an ideal tumor model for studying the interactions between host immunity and cancer cells. CTVTs produce high concentrations of TGF-β to hamper the host immune responses and facilitate their growth progressi...
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Veröffentlicht in: | Veterinary immunology and immunopathology 2009-07, Vol.130 (1), p.25-34 |
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Sprache: | eng |
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Zusammenfassung: | Canine transmissible venereal tumor (CTVT) is a tumor with low MHC antigen expression and is an ideal tumor model for studying the interactions between host immunity and cancer cells. CTVTs produce high concentrations of TGF-β to hamper the host immune responses and facilitate their growth progression. However, during the later stages of tumor progression, tumor-infiltrating lymphocytes secrete IL-6. This cytokine antagonizes TGF-β and restores the IFN-γ activities in promoting MHC antigen expression, and the NK cytotoxicity that has been repressed by TGF-β is also activated. In this study, we applied combinatory treatment of IL-6 plasmid and IL-15 plasmid (
pIL-6/pIL-15) to CTVT-bearing beagles. IL-6 was used as an anti-TGF-β cytokine; IL-15 was used to promote NK- and CTVT-specific cytotoxicity. After intratumoral
pIL-6/pIL-15 delivery mediated by electroporation, MHC antigen expression on CTVT cells was dramatically increased from in less than 5.9% to up to 34% of the tumor cells. The proportion of CD8
+ T cells infiltrating the tumor was also significantly elevated from 6.96
±
0.23% to 21.63
±
5.40%. In addition, the tumor-specific cytotoxicity was enhanced along with a marked increase in tumor-specific IFN-γ-producing cells. These immune responses are believed to be the important forces driving the tumor towards regression. The results indicate that
pIL-6/pIL-15 combinatory immunotherapy may facilitate a promising and effective means of treating tumors. |
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ISSN: | 0165-2427 1873-2534 |
DOI: | 10.1016/j.vetimm.2009.01.002 |