2013
DOI: 10.1371/journal.pone.0080904
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A Trifunctional Dextran-Based Nanovaccine Targets and Activates Murine Dendritic Cells, and Induces Potent Cellular and Humoral Immune Responses In Vivo

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… Show more

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Cited by 25 publications
(16 citation statements)
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“…Dextran is water soluble and is easy to modify with other functional groups to achieve environment responsive properties. Though crystalized dextran particles can serve as vaccine delivery vehicle as reported (Schröder and Ståhl, 1984;Shen et al, 2013), most studies have focused on modified dextran as a candidate for vaccine design. In this section, we discuss only modified dextran.…”
Section: Modified Dextranmentioning
confidence: 99%
“…Dextran is water soluble and is easy to modify with other functional groups to achieve environment responsive properties. Though crystalized dextran particles can serve as vaccine delivery vehicle as reported (Schröder and Ståhl, 1984;Shen et al, 2013), most studies have focused on modified dextran as a candidate for vaccine design. In this section, we discuss only modified dextran.…”
Section: Modified Dextranmentioning
confidence: 99%
“…Incorporation of OVA and lipopolysaccharide in dextran NPs stimulated APCs in a mannose receptor-dependent manner as well as strong cellular (OVA peptide-specific CD4+ and CD8+ T cell) and humoral immune responses in mice [127]. Incorporation of OVA and lipopolysaccharide in dextran NPs stimulated APCs in a mannose receptor-dependent manner as well as strong cellular (OVA peptide-specific CD4+ and CD8+ T cell) and humoral immune responses in mice [127].…”
Section: Dextran and Biopolymer Combinationsmentioning
confidence: 99%
“…Non‐AcDEX did not show any immunostimulatory property per se and was used to co‐encapsulate OVA and lipopolysaccharide into a nanovaccine formulation. It allowed, however, an enhanced uptake by APC in a mannose receptor‐dependent manner, leading to an enhanced immunostimulation in vitro and in vivo …”
Section: Plga Particlesmentioning
confidence: 99%