國家衛生研究院 NHRI:Item 3990099045/8288
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    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/8288


    Title: Development of CpG-Oligodeoxynucleotides for effective activation of rabbit TLR9 mediated immune responses
    Authors: Chuang, TH;Lai, CY;Tseng, PH;Yuan, CJ;Hsu, LC
    Contributors: Immunology Research Center
    Abstract: CpG-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.
    Date: 2014-09-30
    Relation: PLoS ONE. 2014 Sep 30;9(9):Article number e108808.
    Link to: http://dx.doi.org/10.1371/journal.pone.0108808
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=1932-6203&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000343671700167
    Cited Times(Scopus): http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84907486110
    Appears in Collections:[Tsung-Hsien Chuang] Periodical Articles

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