Filamentous bacteriophage fd particles delivering antigenic determinants via DEC-205 (fdsc-?DEC) represent a powerful delivery system that induces CD8(+) T-cell responses even when administered in the absence of adjuvants or maturation stimuli for dendritic cells. In order to investigate the mechanisms of this activity, RNA-Sequencing of fd-pulsed dendritic cells was performed. A significant differential expression of genes involved in innate immunity, co-stimulation and cytokine production was observed. In agreement with these findings, we demonstrate that induction of proinflammatory cytokines and type I interferon by fdsc-?DEC was MYD88 mediated and TLR9 dependent. We also found that fdsc-?DEC is delivered into LAMP-1-positive compartments and co-localizes with TLR9. Thus, phage particles containing a single-strand DNA genome rich in CpG motifs delivered via DEC-205 are able to intercept and trigger the active TLR9 innate immune receptor into late endosome/lysosomes and to enhance the immunogenicity of the displayed antigenic determinants. These findings make fd bacteriophage a valuable tool for immunization without administering exogenous adjuvants.

Antigen delivery by filamentous bacteriophage fd displaying an anti-DEC-205 single-chain variable fragment confers adjuvanticity by triggering a TLR9-mediated immune response.

Sartorius R;D'Apice L;Trovato M;Costa V;Ciccodicola A;
2015

Abstract

Filamentous bacteriophage fd particles delivering antigenic determinants via DEC-205 (fdsc-?DEC) represent a powerful delivery system that induces CD8(+) T-cell responses even when administered in the absence of adjuvants or maturation stimuli for dendritic cells. In order to investigate the mechanisms of this activity, RNA-Sequencing of fd-pulsed dendritic cells was performed. A significant differential expression of genes involved in innate immunity, co-stimulation and cytokine production was observed. In agreement with these findings, we demonstrate that induction of proinflammatory cytokines and type I interferon by fdsc-?DEC was MYD88 mediated and TLR9 dependent. We also found that fdsc-?DEC is delivered into LAMP-1-positive compartments and co-localizes with TLR9. Thus, phage particles containing a single-strand DNA genome rich in CpG motifs delivered via DEC-205 are able to intercept and trigger the active TLR9 innate immune receptor into late endosome/lysosomes and to enhance the immunogenicity of the displayed antigenic determinants. These findings make fd bacteriophage a valuable tool for immunization without administering exogenous adjuvants.
2015
Istituto di genetica e biofisica "Adriano Buzzati Traverso"- IGB - Sede Napoli
Inglese
7
7
973
988
https://www.embopress.org/doi/full/10.15252/emmm.201404525
DEC-205; TLR9; antigen delivery; dendritic cells; filamentous bacteriophage
12
info:eu-repo/semantics/article
262
Sartorius, R; D'Apice, L; Trovato, M; Cuccaro, F; Costa, V; De Leo, Mg; Marzullo, Vm; Biondo, C; D'Auria, S; De Matteis, Ma; Ciccodicola, A; De Berard...espandi
01 Contributo su Rivista::01.01 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/333819
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