佐剂
猪圆环病毒
化学
纳米颗粒
疫苗佐剂
病毒学
氢氧化物
dna疫苗
医学
材料科学
纳米技术
生物化学
免疫学
病毒
重组DNA
有机化学
基因
作者
Qi Zhao,Ziye Zhang,Bowen Song,Jinglu Zhang,Yiliang Li,Ziteng Li,Hongyu Chen,Panpan Xu,Yixuan Zhu,Runyu Yang,Xinghua Zhao,Wanyu Shi,Pengfei Gu
标识
DOI:10.1021/acs.molpharmaceut.5c00716
摘要
Conventional alum adjuvants primarily induce a Th2 humoral immune response yet fail to provoke a Th1 cellular immune response. In our preceding study, we constructed a novel and biosafe nanoparticle-based adjuvant system, in which the Chinese yam polysaccharide (CYP), as the immunopotentiator, was loaded onto aluminum hydroxide nanoparticles (CYP-AlNPs). Herein, we further investigated the adjuvant activity of the CYP-AlNPs against the porcine circovirus type 2 (PCV2) vaccine. Moreover, we further explored the underlying molecular mechanisms by which the CYP-AlNPs stimulated the dendritic cell (DC) activation. Our results demonstrated that the CYP-AlNPs exhibited good adjuvant activity as an adjuvant to the PCV2 vaccine, which elicited a robust antibody response, facilitated the generation of the germinal center in lymph nodes, increased the population of CD4+ and CD8+T cells, and enhanced the production of IFN-γ and IL-6, thereby inducing a mixed Th1 and Th2 immune response. Notably, our results revealed the crucial role of the NLRP3 inflammasome and TLR4-NF-κB signaling pathways in DC activation stimulated by the CYP-AlNPs. The present study highlighted the potential of polysaccharide-alum nanoparticle combination adjuvants that act through different mechanisms to achieve enhanced immune responses, providing a new perspective on vaccine design.
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