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Nanomedicine ; 37: 102445, 2021 10.
Article in English | MEDLINE | ID: mdl-34303841

ABSTRACT

Chikungunya virus (CHIKV) is responsible for a self-limited illness that can evolve into long-lasting painful joint inflammation. In this study, we report a novel experimental CHIKV vaccine formulation of lipid nanoparticles loaded with a recombinant protein derived from the E2 structural protein. This antigen fragment, designated ∆E2.1, maintained the antigenicity of the native viral protein and was specifically recognized by antibodies induced in CHIKV-infected patients. The antigen has been formulated into nanoparticles consisting of nano-multilamellar vesicles (NMVs) combined with the adjuvant monophosphoryl lipid A (MPLA). The vaccine formulation demonstrated a depot effect, leading to controlled antigen release, and induced strong antibody responses significantly higher than in mice immunized with the purified protein combined with the adjuvant. More relevantly, E2-specific antibodies raised in mice immunized with ∆E2.1-loaded NMV-MPLA neutralized CHIKV under in vitro conditions. Taken together, the results demonstrated that the new nanoparticle-based vaccine formulation represents a promising approach for the development of effective anti-CHIKV vaccines.


Subject(s)
Chikungunya Fever/immunology , Chikungunya virus/immunology , Liposomes/immunology , Viral Envelope Proteins/genetics , Animals , Antibodies, Neutralizing/biosynthesis , Antibodies, Neutralizing/drug effects , Antibodies, Neutralizing/immunology , Antibodies, Viral/biosynthesis , Antibodies, Viral/drug effects , Antibodies, Viral/immunology , Chikungunya Fever/therapy , Chikungunya Fever/virology , Chikungunya virus/pathogenicity , Humans , Liposomes/chemistry , Liposomes/pharmacology , Mice , Nanoparticles/chemistry , Viral Envelope Proteins/pharmacology , Viral Vaccines/immunology
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