| Literature DB >> 15531031 |
Holger Bartz1, Yuri Mendoza, Miriam Gebker, Till Fischborn, Klaus Heeg, Alexander Dalpke.
Abstract
CpG-oligonucleotides (CpG-ODN) have been shown to exert strong immuno-stimulatory effects through activation of Toll-like receptor 9 (TLR-9). However, TLR-9 triggering takes place in endosomal compartments and thus CpG-ODN have to be taken up prior to signal transduction. We here report that 3'-poly-guanosine strings can improve cellular internalisation of phosphodiester but not of phosphorothioate CpG-ODN. Improved cellular uptake correlated with enhanced IL-6 secretion and proliferation of PBMC. Also, TLR-9 transfected HEK293 cells were activated more efficiently by poly-guanosine modified CpG-ODN. The results indicate that the synthesis of stimulatory CpG-ODN based on a phosphodiester backbone is feasible via such poly-guanosine substitutions. In addition we observed that phosphorothioate ODN were able to exert immunostimulatory effects independent of the presence of CpG motifs.Entities:
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Year: 2004 PMID: 15531031 DOI: 10.1016/j.vaccine.2004.05.020
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641