佐剂
免疫系统
抗原
卵清蛋白
CpG寡核苷酸
化学
抗原呈递
淋巴结
免疫学
T细胞
生物
生物化学
基因
基因表达
DNA甲基化
作者
Zhengjun Chen,Xinyan Hao,Hairui Wang,Xiaofang Zhong,Xiaohong Chen,Yuanhao Zhao,Yuandong Zhang,Guangsheng Du,Xun Sun
标识
DOI:10.1016/j.jconrel.2022.07.032
摘要
As two of the most widely used adjuvants, aluminum hydroxide and the oil-in-water emulsion MF59 have their intrinsic limitations: classical aluminum gel induces only weak cellular immune responses while MF59 cannot be used as an antigen delivery system due to its poor physical interaction with antigen molecules. Herein, we combined these two adjuvants and constructed a novel nano-vaccine delivery system by inserting aluminum hydroxide into the surface of a modified MF59 nano-emulsion (AlNEs). A model antigen ovalbumin (OVA) and an immune potentiator CpG were adsorbed on the surface of AlNEs (hereinafter AlNEs-OVA-CpG) through a facile mixing step. After subcutaneous injection, AlNEs-OVA-CpG effectively drained to lymph nodes, delivered both cargos into lymph node-resident antigen presenting cells (APCs), and escaped from lysosomes into the cytoplasm, resulting in enhanced antigen cross-presentation. Finally, AlNEs-OVA-CpG induced potent antigen-specific humoral and cellular immune responses, which significantly inhibited tumor growth and prolonged mice survival in a EG7-OVA tumor model. In sum, our results suggested that AlNEs have a great prospect to induce CD8+ T cell responses for subunit antigens.
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