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Nanomedicine ; 37: 102445, 2021 10.
Artigo em Inglês | MEDLINE | ID: mdl-34303841

RESUMO

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.


Assuntos
Febre de Chikungunya/imunologia , Vírus Chikungunya/imunologia , Lipossomos/imunologia , Proteínas do Envelope Viral/genética , Animais , Anticorpos Neutralizantes/biossíntese , Anticorpos Neutralizantes/efeitos dos fármacos , Anticorpos Neutralizantes/imunologia , Anticorpos Antivirais/biossíntese , Anticorpos Antivirais/efeitos dos fármacos , Anticorpos Antivirais/imunologia , Febre de Chikungunya/terapia , Febre de Chikungunya/virologia , Vírus Chikungunya/patogenicidade , Humanos , Lipossomos/química , Lipossomos/farmacologia , Camundongos , Nanopartículas/química , Proteínas do Envelope Viral/farmacologia , Vacinas Virais/imunologia
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