Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-7996
Authors: Shen, Limei
Higuchi, Tetsuya
Tubbe, Ingrid
Voltz, Nicole
Krummen, Mathias
Pektor, Stefanie
Montermann, Evelyn
Rausch, Kristin
Schmidt, Manfred
Schild, Hansjörg
Grabbe, Stephan
Bros, Matthias
Title: A trifunctional dextran-based nanovaccine targets and activates murine dendritic cells, and induces potent cellular and humoral immune responses in vivo
Online publication date: 14-Oct-2022
Year of first publication: 2013
Language: english
Abstract: Dendritic cells (DCs) constitute an attractive target for specific delivery of nanovaccines for immunotherapeutic applications. Here we tested nano-sized dextran (DEX) particles to serve as a DC-addressing nanocarrier platform. Non-functionalized DEX particles had no immunomodulatory effect on bone marrow (BM)-derived murine DCs in vitro. However, when adsorbed with ovalbumine (OVA), DEX particles were efficiently engulfed by BM-DCs in a mannose receptor-dependent manner. A DEX-based nanovaccine containing OVA and lipopolysaccharide (LPS) as a DC stimulus induced strong OVA peptide-specific CD4(+) and CD8(+) T cell proliferation both in vitro and upon systemic application in mice, as well as a robust OVA-specific humoral immune response (IgG1>IgG2a) in vivo. Accordingly, this nanovaccine also raised both a more pronounced delayed-type hypersensitivity response and a stronger induction of cytotoxic CD8(+) T cells than obtained upon administration of OVA and LPS in soluble form. Therefore, DEX-based nanoparticles constitute a potent, versatile and easy to prepare nanovaccine platform for immunotherapeutic approaches.
DDC: 610 Medizin
610 Medical sciences
Institution: Johannes Gutenberg-Universität Mainz
Department: FB 04 Medizin
FB 09 Chemie, Pharmazie u. Geowissensch.
Place: Mainz
ROR: https://ror.org/023b0x485
DOI: http://doi.org/10.25358/openscience-7996
Version: Published version
Publication type: Zeitschriftenaufsatz
License: CC BY
Information on rights of use: https://creativecommons.org/licenses/by/3.0/
Journal: PLoS one
8
12
Pages or article number: e80904
Publisher: PLoS
Publisher place: Lawrence, Kan.
Issue date: 2013
ISSN: 1932-6203
Publisher URL: http://dx.doi.org/10.1371/journal.pone.0080904
Publisher DOI: 10.1371/journal.pone.0080904
Appears in collections:DFG-OA-Publizieren (2012 - 2017)

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