Vaccination with human papillomavirus type 16-derived peptides using a tattoo device
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
19464530
DOI
10.1016/j.vaccine.2009.03.073
PII: S0264-410X(09)00506-4
Knihovny.cz E-zdroje
- MeSH
- cytotoxické T-lymfocyty imunologie MeSH
- DNA vakcíny imunologie MeSH
- hemokyanin imunologie MeSH
- lidský papilomavirus 16 imunologie MeSH
- molekulární sekvence - údaje MeSH
- myši inbrední C57BL MeSH
- myši MeSH
- onkogenní proteiny virové imunologie MeSH
- Papillomavirus E7 - proteiny MeSH
- peptidové fragmenty imunologie MeSH
- represorové proteiny imunologie MeSH
- sekvence aminokyselin MeSH
- tetování přístrojové vybavení MeSH
- vakcinace * MeSH
- vakcíny proti papilomavirům imunologie MeSH
- virové plášťové proteiny imunologie MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- DNA vakcíny MeSH
- E6 protein, Human papillomavirus type 16 MeSH Prohlížeč
- hemokyanin MeSH
- keyhole-limpet hemocyanin MeSH Prohlížeč
- L2 protein, Human papillomavirus type 16 MeSH Prohlížeč
- oncogene protein E7, Human papillomavirus type 16 MeSH Prohlížeč
- onkogenní proteiny virové MeSH
- Papillomavirus E7 - proteiny MeSH
- peptidové fragmenty MeSH
- represorové proteiny MeSH
- vakcíny proti papilomavirům MeSH
- virové plášťové proteiny 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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