Abstract
Dendritic cells (DC) enhanced the immunogenicity of recombinant vaccinia viruses (rVV) expressing the E7 protein of HPV16, a tumor-associated antigen (TAA). Immunization with DC transduced by rVV generated from strain Praha or MVA induced better protection against the growth of transplanted TC-1 tumors in C57Bl/6 mice than did immunization with either of these rVVs administered alone by the same route. Interestingly, DC transduced with a double recombinant vaccinia virus expressing E7 protein together with the Th1-polarizing cytokine IL12, which has been shown to enhance the cellular response in several other systems, induced lower anti-tumor immunity than DC transduced with rVV expressing E7 protein alone. The inhibitory effect mediated by IL12 on immunization with rVV-infected DC was dose-dependent and was observed after immunization with DC transduced with IL12-expressing rVV even at low multiplicity.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Adjuvants, Immunologic
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Animals
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Antigen Presentation
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Cancer Vaccines / immunology
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Cancer Vaccines / therapeutic use
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Dendritic Cells / immunology*
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Female
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Genetic Therapy*
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Genetic Vectors
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Humans
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Immunization
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Immunotherapy*
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Interleukin-12 / genetics
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Interleukin-12 / immunology
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Interleukin-12 / therapeutic use*
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Mice
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Mice, Inbred C57BL
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Neoplasms, Experimental / immunology
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Neoplasms, Experimental / therapy*
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Neoplasms, Experimental / virology
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Oncogene Proteins, Viral / genetics
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Oncogene Proteins, Viral / immunology
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Oncogene Proteins, Viral / therapeutic use*
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Papillomaviridae / physiology
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Papillomavirus E7 Proteins
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Papillomavirus Infections / genetics
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Papillomavirus Infections / immunology
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Papillomavirus Infections / therapy
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Survival Rate
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Th1 Cells / immunology
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Transduction, Genetic
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Vaccinia virus / genetics*
Substances
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Adjuvants, Immunologic
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Cancer Vaccines
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Oncogene Proteins, Viral
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Papillomavirus E7 Proteins
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oncogene protein E7, Human papillomavirus type 16
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Interleukin-12