Abstract
Enhancing immune response activation through the synergy of effective antigen delivery and immune enhancement using natural, biodegradable materials with immune-adjuvant capabilities is challenging. Here, we present NAPS(L.p) that can activate the Toll-like receptor 4 (TLR4) pathway, an amphiphilic exopolysaccharide, as a potential self-assembly adjuvant delivery platform. Its molecular structure and unique properties exhibited remarkable self-assembly, forming a homogeneous nanovaccine with ovalbumin (OVA) as the model antigen. When used as an adjuvant, NAPS(L.p) significantly increased OVA uptake by dendritic cells. In vivo imaging revealed prolonged pharmacokinetics of NAPS(L. p)-delivered OVA compared to OVA alone. Notably, NAPS(L.p) induced elevated levels of specific serum IgG and isotype titers, enhancing rejection of B16-OVA melanoma xenografts in vaccinated mice. Additionally, NAPS(L.p) formulation improved therapeutic effects, inhibiting tumor growth, and increasing animal survival rates. The nanovaccine elicited CD4(+) and CD8(+) T cell-based immune responses, demonstrating the potential for melanoma prevention. Furthermore, NAPS(L.p)-based vaccination showed stronger protective effects against influenza compared to Al (OH)(3) adjuvant. Our findings suggest NAPS(L.p) as a promising, natural self-adjuvanting delivery platform to enhance vaccine design across applications.