Abstract

Malaria is a life-threatening global epidemic disease and has caused more than 400,000 deaths in 2019. To control and prevent malaria, the development of a vaccine is a potential method. An effective malaria vaccine should either combine antigens from all stages of the malaria parasite’s life cycle, or epitopes of multiple key antigens due to the complexity of the Plasmodium parasite. Malaria’s random constructed antigen-1 (M.RCAg-1) is one of the recombinant vaccines, which was selected from a DNA library containing thousands of diverse multi-epitope chimeric antigen genes. Moreover, besides selecting an antigen, using an adjuvant is another important procedure for most vaccine development procedures. Freund’s adjuvant is considered an effective vaccine adjuvant for malaria vaccine, but it cannot be used in clinical settings because of its serious side effects. Traditional adjuvants, such as alum adjuvant, are limited by their unsatisfactory immune effects in malaria vaccines, hence there is an urgent need to develop a novel, safe and efficient adjuvant. In recent years, Pickering emulsions have attracted increasing attention as novel adjuvant. In contrast to classical emulsions, Pickering emulsions are stabilized by solid particles instead of surfactant, having pliability and lateral mobility. In this study, we selected aluminum hydroxide gel (termed as “alum”) as a stabilizer to prepare alum-stabilized Pickering emulsions (ALPE) as a malaria vaccine adjuvant. In addition, monophosphoryl lipid A (MPLA) as an immunostimulant was incorporated into the Pickering emulsion (ALMPE) to further enhance the immune response. In vitro tests showed that, compared with alum, ALPE and ALMPE showed higher antigen load rates and could be effectively endocytosed by J774a.1 cells. In vivo studies indicated that ALMPE could induce as high antibody titers as Freund’s adjuvant. The biocompatibility study also proved ALMPE with excellent biocompatibility. These results suggest that ALMPE is a potential adjuvant for a malaria vaccine.

Highlights

  • These results suggest that ALMPE is a potential adjuvant for a malaria vaccine

  • Is comprised of AS01 and hepatitis B virus surface antigen (HBsAg) virus-like particles incorporating a portion of the Plasmodium falciparum-derived circumsporozoite protein (CSP) genetically fused to HBsAg, which have proven to have bactericidal immunity in mice [4,5]

  • It is anticipated that monophosphorylate lipid A (MPLA)-loaded Pickering emulsion may serve as an effective adjuvant for an enhanced malaria M.RCAg-1 vaccine

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Summary

Introduction

Eight of the 11 epitope peptides are in the intra-erythrocyte stage, so the antibodies produced in animal experiments can inhibit the growth of Plasmodium falciparum [11]. A multi-epitope chimeric antigen M.RCAg-1 demonstrated the great efficacy of inhibiting the parasites growth in animal models [12]. M.RCAg-1 was composed of eleven key epitope peptides of Plasmodium falciparum and could be cheaply expressed in E. coli in soluble form. Alum adjuvant has been applied widely as a traditional commercial adjuvant, but it’s immune effect is not significant for malaria vaccine [17,18]. It is anticipated that MPLA-loaded Pickering emulsion may serve as an effective adjuvant for an enhanced malaria M.RCAg-1 vaccine. In vitro and in vivo experiments were performed to evaluate the adjuvant effect of Pickering emulsions using OVA and M.RCAg-1 as model antigen

Materials
Preparation of Pickering Emulsions
Characterization of Pickering Emulsions
Evaluation the Antigen Intracellular Distribution
Vaccination
Determination
ELISPOT Assay
Statistical Analysis
Pickering Emulsions by Using Alum as Stabilizer
Effect Particle Concentration on Pickering Emulsions
It is illustrated the droplet size obtained byH using
Effect the pH of the Aqueous Phase on Emulsion
Characterization of ALPE and ALMPE
Characteristics
Cytosolic Localization
10. Systemic
Safety and Biocompatibility
Conclusions
Full Text
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