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Int J Nanomedicine ; 15: 3877-3886, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-32581535

RESUMEN

INTRODUCTION: Vaccine formulation with appropriate adjuvants is an attractive approach to develop protective immunity against pathogens. Calcium phosphate nanoparticles (CaPNs) are considered as ideal adjuvants and delivery systems because of their great potential for enhancing immune responses. In the current study, we have designed nanoparticle-based vaccine candidates to induce immune responses and protection against B. melitensis and B. abortus. MATERIALS AND METHODS: For this purpose, we used three Brucella antigens (FliC, 7α-HSDH, BhuA) and two multi-epitopes (poly B and poly T) absorbed by CaPNs. The efficacy of each formulation was evaluated by measuring humoral, cellular and protective responses in immunized mice. RESULTS: The CaPNs showed an average size of about 90 nm with spherical shape and smooth surface. The CaPNs-adsorbed proteins displayed significant increase in cellular and humoral immune responses compared to the control groups. In addition, our results showed increased ratio of specific IgG2a (associated with Th1) to specific IgG1 (associated with Th2). Also, immunized mice with different vaccine candidate formulations were protected against B. melitensis 16M and B. abortus 544, and showed same levels of protection as commercial vaccines (B. melitensis Rev.1 and B. abortus RB51) except for BhuA-CaPNs. DISCUSSION: Our data support the hypothesis that these antigens absorbed with CaPNs could be effective vaccine candidates against B. melitensis and B. abortus.


Asunto(s)
Antígenos Bacterianos/química , Vacuna contra la Brucelosis/química , Vacuna contra la Brucelosis/inmunología , Nanopartículas/química , Adyuvantes Inmunológicos/administración & dosificación , Adyuvantes Inmunológicos/farmacología , Animales , Proteínas Bacterianas/inmunología , Brucella abortus/inmunología , Brucella melitensis/inmunología , Brucelosis/inmunología , Brucelosis/prevención & control , Fosfatos de Calcio/química , Sistemas de Liberación de Medicamentos , Femenino , Inmunidad Humoral , Inmunización , Inmunoglobulina G/inmunología , Proteínas de Transporte de Membrana/inmunología , Ratones Endogámicos BALB C
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