Vaccination with human papillomavirus type 16-derived peptides using a tattoo device
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
19464530
DOI
10.1016/j.vaccine.2009.03.073
PII: S0264-410X(09)00506-4
Knihovny.cz E-resources
- MeSH
- T-Lymphocytes, Cytotoxic immunology MeSH
- Vaccines, DNA immunology MeSH
- Hemocyanins immunology MeSH
- Human papillomavirus 16 immunology MeSH
- Molecular Sequence Data MeSH
- Mice, Inbred C57BL MeSH
- Mice MeSH
- Oncogene Proteins, Viral immunology MeSH
- Papillomavirus E7 Proteins MeSH
- Peptide Fragments immunology MeSH
- Repressor Proteins immunology MeSH
- Amino Acid Sequence MeSH
- Tattooing instrumentation MeSH
- Vaccination * MeSH
- Papillomavirus Vaccines immunology MeSH
- Capsid Proteins immunology MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Vaccines, DNA MeSH
- E6 protein, Human papillomavirus type 16 MeSH Browser
- Hemocyanins MeSH
- keyhole-limpet hemocyanin MeSH Browser
- L2 protein, Human papillomavirus type 16 MeSH Browser
- oncogene protein E7, Human papillomavirus type 16 MeSH Browser
- Oncogene Proteins, Viral MeSH
- Papillomavirus E7 Proteins MeSH
- Peptide Fragments MeSH
- Repressor Proteins MeSH
- Papillomavirus Vaccines MeSH
- Capsid Proteins MeSH
Tattooing has been shown to be very efficient at inducing immunity by vaccination with DNA vaccines. In this study, we examined the usability of tattooing for delivery of peptide vaccines. We compared tattooing with subcutaneous (s.c.) needle injection using peptides derived from human papillomavirus type 16 (HPV16) proteins. We observed that higher peptide-specific immune responses were elicited after vaccination with the simple peptides (E7(44-62) and E7(49-57)) and keyhole limpet hemocyanin-(KLH)-conjugated peptides (E7(49-57), L2(18-38) and L2(108-120)) with a tattoo device compared to s.c. inoculation. The administration of the synthetic oligonucleotide containing immunostimulatory CpG motifs (ODN1826) enhanced the immune responses developed after s.c. injection of some peptides (E7(44-62), KLH-conjugated L2(18-38) and L2(108-120)) to levels close to or even comparable to those after tattoo delivery of identical peptides with ODN1826. The highest efficacy of tattooing was observed in combination with ODN1826 for the vaccination with the less immunogenic E6(48-57) peptide and KLH-conjugated and non-conjugated E7(49-57) peptides which form the visible aggregates that could negatively influence the development of immune responses after s.c. injection but probably not after tattooing. In summary, we first evidenced that tattoo administration of peptide vaccines that might be useful in some cases efficiently induced both humoral and cell-mediated immune responses.
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