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Adjuvating the adjuvant: facilitated delivery of an immunomodulatory oligonucleotide to TLR9 by a cationic antimicrobial peptide in dendritic cells
Authors:Aichinger Michael C  Ginzler Michael  Weghuber Julian  Zimmermann Lars  Riedl Karin  Schütz Gerhard  Nagy Eszter  von Gabain Alexander  Schweyen Rudolf  Henics Tamás
Affiliation:a Department of Genetics, Max F. Perutz Laboratories, Dr. Bohrgasse 9, 1030 Vienna, Austria
b INTERCELL AG, Campus Vienna Biocenter 3, 1030 Vienna, Austria
c Biophysics Institute, Johannes Kepler University, Altenbergstrasse 69, 4040 Linz, Austria
Abstract:IC31® 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 immuno-modulating 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.
Keywords:Adjuvant   Cationic antimicrobial peptide   Dendritic cell
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