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Systemic administration of CpG oligodeoxynucleotide and levamisole as adjuvants for gene-gun-delivered antitumor DNA vaccines
M. Šmahel, I. Poláková, E. Sobotková, E. Vajdová
Jazyk angličtina Země Egypt
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Directory of Open Access Journals
od 2003
Free Medical Journals
od 1990
PubMed Central
od 2003 do 2013
Europe PubMed Central
od 2003 do 2013
Open Access Digital Library
od 2003-01-01 do 2013-12-31
Open Access Digital Library
od 2003-01-01 do 2013-12-31
Open Access Digital Library
od 2003-01-01
Medline Complete (EBSCOhost)
od 2003-03-01 do 2013-01-31
ROAD: Directory of Open Access Scholarly Resources
od 2003 do 2013
PubMed
22028727
DOI
10.1155/2011/176759
Knihovny.cz E-zdroje
- MeSH
- adjuvancia imunologická aplikace a dávkování MeSH
- bcr-abl fúzní proteiny genetika imunologie metabolismus MeSH
- biolistika MeSH
- CD8-pozitivní T-lymfocyty účinky léků metabolismus patologie MeSH
- DNA vakcíny MeSH
- experimentální nádory imunologie patologie terapie MeSH
- imunita účinky léků MeSH
- levamisol aplikace a dávkování MeSH
- lidé MeSH
- modely nemocí na zvířatech MeSH
- myši inbrední BALB C MeSH
- myši inbrední C57BL MeSH
- myši MeSH
- nádorové buněčné linie MeSH
- oligodeoxyribonukleotidy aplikace a dávkování MeSH
- Papillomavirus E7 - proteiny genetika imunologie metabolismus MeSH
- protinádorové vakcíny MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
DNA vaccines showed great promise in preclinical models of infectious and malignant diseases, but their potency was insufficient in clinical trials and is needed to be improved. In this study, we tested systemic administration of two conventional adjuvants, synthetic oligodeoxynucleotide carrying immunostimulatory CpG motifs (CpG-ODN) and levamisole (LMS), and evaluated their effect on immune reactions induced by DNA vaccines delivered by a gene gun. DNA vaccination was directed either against the E7 oncoprotein of human papillomavirus type 16 or against the BCR-ABL1 oncoprotein characteristic for chronic myeloid leukemia. High doses of both adjuvants reduced activation of mouse splenic CD8(+) T lymphocytes, but the overall antitumor effect was enhanced in both tumor models. High-dose CpG-ODN exhibited a superior adjuvant effect in comparison with any combination of CpG-ODN with LMS. In summary, our results demonstrate the benefit of combined therapy with gene-gun-delivered antitumor DNA vaccines and systemic administration of CpG-ODN or LMS.
Citace poskytuje Crossref.org
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