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dc.contributor.authorChuang, Tsung-Hsienen_US
dc.contributor.authorLai, Chao-Yangen_US
dc.contributor.authorTseng, Ping-Huien_US
dc.contributor.authorYuan, Chiun-Jyeen_US
dc.contributor.authorHsu, Li-Chungen_US
dc.date.accessioned2014-12-08T15:36:58Z-
dc.date.available2014-12-08T15:36:58Z-
dc.date.issued2014-09-30en_US
dc.identifier.issn1932-6203en_US
dc.identifier.urihttp://dx.doi.org/10.1371/journal.pone.0108808en_US
dc.identifier.urihttp://hdl.handle.net/11536/25367-
dc.description.abstractCpG-oligodeoxynucleotides (CpG-ODN) are potent immune stimuli being developed for use as adjuvants in different species. Toll-like receptor 9 (TLR9) is the cellular receptor for CpG-ODN in mammalian cells. The CpG-ODN with 18-24 deoxynucleotides that are in current use for human and mouse cells, however, have low activity with rabbit TLR9. Using a cell-based activation assay, we developed a type of CpG-ODN containing a GACGTT or AACGTT motif in 12 phosphorothioate-modified deoxynucleotides with potent stimulatory activity for rabbit TLR9. The developed CpG-ODN have higher activities than other developed CpG-ODN in eliciting antigen-nonspecific immune responses in rabbit splenocytes. When mixed with an NJ85 peptide derived from rabbit hemorrhagic disease virus, they had potent activities to boost an antigen-specific T cell activation and antibody production in rabbits. Compared to Freund\'s adjuvant, the developed CpG-ODN are capable of boosting a potent and less toxic antibody response. The results of this study suggest that both the choice of CpG-motif and its length are important factors for CpG-ODN to effectively activate rabbit TLR9 mediated immune responses.en_US
dc.language.isoen_USen_US
dc.titleDevelopment of CpG-Oligodeoxynucleotides for Effective Activation of Rabbit TLR9 Mediated Immune Responsesen_US
dc.typeArticleen_US
dc.identifier.doi10.1371/journal.pone.0108808en_US
dc.identifier.journalPLOS ONEen_US
dc.citation.volume9en_US
dc.citation.issue9en_US
dc.citation.epageen_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000343671700167-
dc.citation.woscount1-
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