Abstract
Virus-like particles (VLPs) have emerged as promising vaccine candidates against foot-and-mouth disease (FMD). However, such vaccines provide a relatively low level of protection against FMD virus (FMDV) because of their poor immunogenicity. Therefore, it is necessary to design effective vaccine strategies that induce more potent immunogenicity. In order to investigate the means to improve FMD VLP vaccine (VLP(FMDV)) immunogenicity, we encapsulated VLPs (MPL/DDA-VLP(FMDV)) with cationic liposomes based on dimethyldioctadecylammonium bromide (DDA) and/or monophosphoryl lipid A (MPL, TLR4 agonist) as adjuvants. Unlike inactivated whole-cell vaccines, VLP(FMDV) were successfully encapsulated in this MPL/DDA system. We found that MPL/DDA-VLP(FMDV) could induce strong cell-mediated immune responses by inducing not only VLP-specific IFN-γ(+)CD4(+) (Th1), IL-17A(+)CD4(+) (Th17), and IFN-γ(+)CD8(+) (activated CD8 response) T cells, but also the development of VLP-specific multifunctional CD4(+) and CD8(+) memory T cells co-expressing IFN-γ, TNF-α, and IL-2. In addition, the MPL/DDA-VLP(FMDV) vaccine markedly induced VLP-specific antibody titers; in particular, the vaccine induced greater Th1-predominant IgG responses than VLP(FMDV) only and DDA-VLP(FMDV). These results are expected to provide important clues for the development of an effective VLP(FMDV) that can induce cellular and humoral immune responses, and address the limitations seen in current VLP vaccines for various diseases.