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1.
Exp Oncol ; 30(4): 319-23, 2008 Dec.
Article in English | MEDLINE | ID: mdl-19112431

ABSTRACT

AIM: To study in vivo efficacy of combined administration of cancer vaccine (CV), interferon (IFN) and inducer of endogenous IFN - amixin. MATERIALS AND METHODS: Sarcoma-37 cells were transplanted to female Balb/c mice. For the treatment, CV prepared from sarcoma-37 cells with the use of cytotoxic lectines from B. subtilis B-7025, murine IFN and amixin or their combinations were used. IFN production, content of circulating immune complexes and level of specific IgG antibodies in blood serum were determined by standard immunologic methods. RESULTS: Using solid form of sarcoma-37 it has been shown that introduction of IFN and amixin significantly elevated efficacy of vaccine therapy, in particular index of tumor growth inhibition reach 89.2% and 81.7%. Upon combined use of CV and IFN or CV and amixin (25 mg/kg) respectively. Significant prolongation of average life span of the animals treated with CV and IFN or CV and amixin (25 mg/kg) has been registered (up to 92.7 -/+ 10.4 and 95.0 -/+ 6.2 days respectively, vs 46.8 -/+ 1.5 days for control animals). CONCLUSION: Obtained results have shown expediency of the development of schemes for combined introduction of CV with exogenous IFN, and with inducer of endogenous IFN (amixin) for elevation of efficacy of vaccine therapy.


Subject(s)
Cancer Vaccines/immunology , Immunotherapy/methods , Interferon Inducers/administration & dosage , Interferons/administration & dosage , Sarcoma/drug therapy , Tilorone/administration & dosage , Animals , Cancer Vaccines/therapeutic use , Female , Interferon Inducers/immunology , Interferons/immunology , Mice , Mice, Inbred BALB C , Tilorone/immunology
2.
Exp Oncol ; 29(2): 102-5, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17704740

ABSTRACT

AIM: To study in in vivo model the efficacy of combined scheme of administration of cancer vaccine (CV) and interferon (IFN). MATERIALS AND METHODS: Lewis lung carcinoma (LLC) was transplanted to male C57Bl mice. For treatment, CV prepared from LLC cells with the use of cytotoxic lectins of B. subtilis B-7025, and preparation of murine IFN-alpha were used. Therapeutic effect was evaluated by measurement of tumor volume and analysis of average life span (ALS) of treated animals. Immunologic study included determination of antitumor cytotoxicity of T-lymphocytes (CTL) and natural killer (NK) cells by radiometric method, functional activity of peritoneal macrophages (MP) - by colorimetric test with nitroazole blue, and evaluation of titers of tumor necrosis factor (TNF) and interleukins-1 and -2 (IL-1, 2). RESULTS: It has been shown that the use of IFN preparation significantly elevated efficacy of vaccine therapy of solid form of LLC: duration of latent period of tumor growth elevated by 25%, ALS - by 28%, index of tumor growth inhibition - by 35-40%. Upon combined use of CV and IFN, significant activation of the cells - effectors of nonspecific immune defense (MP), and specific one (CTL) was observed. CONCLUSION: The obtained results evidence on perspectiveness of the development of combined schemes of administration of CV and IFN for elevation of the efficacy of vaccine therapy.


Subject(s)
Cancer Vaccines/therapeutic use , Carcinoma, Lewis Lung/therapy , Interferon-alpha/therapeutic use , Lung Neoplasms/therapy , Animals , Cancer Vaccines/administration & dosage , Carcinoma, Lewis Lung/immunology , Cytotoxicity Tests, Immunologic , Drug Synergism , Drug Therapy, Combination , Interferon-alpha/administration & dosage , Interleukin-1/blood , Interleukin-2/blood , Killer Cells, Natural/drug effects , Lung Neoplasms/immunology , Lymphocyte Activation/drug effects , Lymphocyte Activation/immunology , Macrophage Activation/drug effects , Macrophage Activation/immunology , Macrophages, Peritoneal/drug effects , Male , Mice , Mice, Inbred C57BL , Neoplasm Transplantation , Survival Rate , T-Lymphocytes, Cytotoxic/drug effects , Time Factors , Transplantation, Homologous , Tumor Burden/drug effects , Tumor Necrosis Factor-alpha/biosynthesis
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