Adjuvating the adjuvant: Facilitated delivery of an immunomodulatory oligonucleotide to TLR9 by a cationic antimicrobial peptide in dendritic cells

被引:30
作者
Aichinger, Michael C. [1 ]
Ginzler, Michael [2 ]
Weghuber, Julian [3 ]
Zimmermann, Lars [3 ]
Riedl, Karin [2 ]
Schuetz, Gerhard [3 ]
Nagy, Eszter [2 ]
von Gabain, Alexander [2 ]
Schweyen, Rudolf [1 ]
Henics, Tamas [1 ]
机构
[1] Max F Perutz Labs, Dept Genet, A-1030 Vienna, Austria
[2] INTERCELL AG, A-1030 Vienna, Austria
[3] Johannes Kepler Univ Linz, Inst Biophys, A-4040 Linz, Austria
关键词
Adjuvant; Cationic antimicrobial peptide; Dendritic cell; ACTIVATION; PROTEIN; ER;
D O I
10.1016/j.vaccine.2010.11.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
IC31 (R) is a novel bi-component vaccine adjuvant consisting of the peptide KLKL5KLK (KLK) and the TLR9 agonist oligonucleotide d(IC)(13) (ODN1a). While membrane-interacting properties of KLK and immunomodulating capabilities of ODN1a have been characterized in detail, little is known of how these two molecules function together and synergize in interacting with their primary target cells, dendritic cells (DCs). We have found that KLK-triggered aggregates entrapped ODN1a and these complexes readily associated with the DC cell surface. KLK stimulated the uptake and internalization of ODN1a via endocytosis, while the bulk of the peptide remained associated with the cell periphery. ODN1a co-localized with early and late endosomes as well as endoplasmic reticular structures. ODN1a co-localized with TLR9 positive compartments following KLK mediated uptake. These features did not depend on the expression of TLR-9. Our results reveal novel mechanisms that allow KLK to enhance the effects of the TLR-9 ligand ODN1a in immunomodulation. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:426 / 436
页数:11
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