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Virology ; 395(1): 45-55, 2009 Dec 05.
Article in English | MEDLINE | ID: mdl-19800648

ABSTRACT

Here we report a novel strategy for the induction of CD8(+) T cell adaptive immune response against viral and tumor antigens. This approach relies on high levels of incorporation in HIV-1 VLPs of a mutant of HIV-1 Nef (Nef(mut)) which can act as anchoring element for foreign proteins. By in vitro assay, we found that VLP-associated Nef(mut) is efficiently cross-presented by antigen presenting cells. Inoculation in mice of VLPs incorporating the HPV-16 E7 protein fused to Nef(mut) led to an anti-E7 CD8(+) T cell response much stronger than that elicited by E7 recombinant protein inoculated with incomplete Freund's adjuvant and correlating with well-detectable anti-E7 CTL activity. Most relevantly, mice immunized with Nef(mut)-E7 VLPs developed a protective immune response against tumors induced by E7 expressing tumor cells. These results make Nef(mut) VLPs a promising candidate for new vaccine strategies focused on the induction of CD8(+) T cell immunity.


Subject(s)
CD8-Positive T-Lymphocytes/immunology , Cancer Vaccines/immunology , Oncogene Proteins, Viral/immunology , nef Gene Products, Human Immunodeficiency Virus/immunology , Adaptive Immunity , Animals , Cell Line , Cross-Priming , HIV-1/immunology , Human papillomavirus 16/immunology , Humans , Membrane Glycoproteins/immunology , Mice , Mice, Inbred C57BL , Papillomavirus E7 Proteins , Papillomavirus Infections/prevention & control , Papillomavirus Vaccines/immunology , Recombinant Fusion Proteins/immunology , Vesicular stomatitis Indiana virus/immunology , Viral Envelope Proteins/immunology
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