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IC31, a novel adjuvant signaling via TLR9, induces potent cellular and humoral immune responses.

作者信息

Schellack Carola, Prinz Karin, Egyed Alena, Fritz Jörg H, Wittmann Barbara, Ginzler Michael, Swatosch Gabriele, Zauner Wolfgang, Kast Constantia, Akira Shizuo, von Gabain Alexander, Buschle Michael, Lingnau Karen

机构信息

Intercell AG, Campus Vienna Biocenter 6, 1030 Wien, Austria.

出版信息

Vaccine. 2006 Jun 29;24(26):5461-72. doi: 10.1016/j.vaccine.2006.03.071. Epub 2006 Apr 7.

DOI:10.1016/j.vaccine.2006.03.071
PMID:16678312
Abstract

IC31, the combination of a novel immunostimulatory oligodeoxynucleotide containing deoxy-Inosine/deoxy-Cytosine (ODN1a) and the antimicrobial peptide KLKL(5)KLK, represents a promising novel adjuvant signaling via the TLR9/MyD88-dependent pathway of the innate immune system. In mice, IC31 induces potent peptide-specific type 1 cellular immune responses, as well as mainly type 1 dominated protein-specific cellular and humoral immune responses. In addition, cytotoxic T lymphocytes were induced, able to kill efficiently target cells in vivo. Activation of murine dendritic cells by IC31 induced efficiently proliferation of naïve CD4(+) TCR transgenic T cells (DO.11.10) as well as their differentiation into IFN-gamma- and IL-4-producing T cells in vitro.

摘要

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