Probiotic-derived amphiphilic exopolysaccharide self-assembling adjuvant delivery platform for enhancing immune responses

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 that can activate the Toll-like receptor 4 (TLR4) pathway, an amphiphilic exopo...

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Veröffentlicht in:Journal of nanobiotechnology 2024-05, Vol.22 (1), p.267-267, Article 267
Hauptverfasser: Sheng, Shouxin, Zhang, Haochi, Li, Xinyu, Chen, Jian, Wang, Pu, Liang, Yanchen, Li, Chunhe, Li, Haotian, Pan, Na, Bao, Xuemei, Liu, Mengnan, Zhao, Lixia, Li, Xiaoyan, Guan, Pingyuan, Wang, Xiao
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Sprache:eng
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Zusammenfassung: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 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 significantly increased OVA uptake by dendritic cells. In vivo imaging revealed prolonged pharmacokinetics of NAPS -delivered OVA compared to OVA alone. Notably, NAPS induced elevated levels of specific serum IgG and isotype titers, enhancing rejection of B16-OVA melanoma xenografts in vaccinated mice. Additionally, NAPS 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 -based vaccination showed stronger protective effects against influenza compared to Al (OH) adjuvant. Our findings suggest NAPS as a promising, natural self-adjuvanting delivery platform to enhance vaccine design across applications.
ISSN:1477-3155
1477-3155
DOI:10.1186/s12951-024-02528-y