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Int J Biol Macromol ; 270(Pt 1): 132432, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38761609

ABSTRACT

The African swine fever virus (ASFV) continues to pose significant economic and pandemic risks. Consequently, discovering new, efficient vaccines is crucial. Messenger RNA (mRNA) vaccines have emerged as promising candidates, providing minimal risk of insertional mutagenesis, high safety profiles, effectiveness, rapid scalability in production, and cost-effectiveness. In this study, we have developed an ASF p30 mRNA vaccine candidate (mRNA/Man-LNP) employing mannose-modified lipid nanoparticles (LNPs). The mRNA/Man-LNP exhibited effective antigen presentation and facilitated dendritic cells (DCs) maturation. Notably, it elicited strong IgG titers and activated CD4+ and CD8+ T-cells in immunized mice, all while adhering to stringent biosafety standards. This investigation demonstrates that mRNA/Man-LNP can trigger both humoral and cellular immune responses, suggesting its potential as a potent and promising vaccine candidate for controlling African swine fever (ASF).


Subject(s)
African Swine Fever Virus , African Swine Fever , Mannose , Nanoparticles , Viral Vaccines , Animals , Nanoparticles/chemistry , African Swine Fever Virus/immunology , African Swine Fever Virus/genetics , African Swine Fever/prevention & control , African Swine Fever/immunology , Mice , Viral Vaccines/immunology , Swine , Mannose/chemistry , Dendritic Cells/immunology , Lipids/chemistry , Vaccine Development , RNA, Messenger/genetics , RNA, Messenger/immunology , mRNA Vaccines , Female , Antibodies, Viral/immunology , Antibodies, Viral/blood , Liposomes
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