皮克林乳剂佐剂对新冠肺炎多肽疫苗免疫效果的影响

Zhuanqing Huang , Qi Sun , Haoyuan Shi , Sen Yang , Yuanyuan Li , Yue Ma , Fei Yang , Zhenwei Shi , Yalong Yang , Ying Zhang , Hui Gong , Fenghua Xu
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引用次数: 0

摘要

以角鲨烯为油相,铝助剂为颗粒稳定剂,在冰水浴中超声乳化制备了Pickering乳液。研究了配方和工艺条件对Pickering乳液尺寸和分布的影响。将在最佳处方和工艺条件下制备的Pickering乳液与肽抗原混合以获得肽疫苗。Pickering乳液的最佳处方和工艺条件为:角鲨烯为油相,超纯水为水相,铝助剂为5mg/mL,超声时间为4min,功率为200W。用肽疫苗免疫BALB/c小鼠,并评价Pickering乳液作为免疫佐剂提高肽疫苗效力的能力。在最佳条件下,获得了粒径小(430.8nm)、分布均匀(多分散指数为16.9%)、ζ电位为31.5mV的Pickering乳液。免疫结果表明,接种组经三次免疫后血清特异性抗体水平达到1×104。接种组中CD4+T细胞和CD4/CD8细胞的比例显著高于空白对照组(P<;0.05)。此外,细胞因子(TNF-α)分泌在铝佐剂和Pickering乳液组中减少,但在弗氏佐剂组中增加。所有三组接种疫苗的小鼠都表现出低但可检测的IFN-γ分泌水平。
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The effect of Pickering emulsion adjuvants on the immune efficacy of the COVID-19 polypeptide vaccine

Pickering emulsions were prepared by phacoemulsification in an ice water bath with squalene as the oil phase and an aluminum adjuvant as the particle stabilizer. The effects of formulation and process conditions on the size and distribution of the Pickering emulsions were investigated. Pickering emulsions prepared under the optimal prescription and process conditions were mixed with a peptide antigen to obtain a peptide vaccine. The optimal prescription and process condition of the Pickering emulsion is as follows: squalene as the oil phase, ultra-pure water as the water phase with 5 mg/mL aluminum adjuvant, and an ultrasonication time of 4 min at 200 W power. BALB/c mice were immunized with the peptide vaccine, and the ability of the Pickering emulsion as an immunological adjuvant to improve the efficacy of the peptide vaccine was evaluated. Under optimal conditions, a Pickering emulsion with a small particle size (430.8 nm), uniform distribution (polydispersion index of 16.9%), and zeta potential of 31.5 mV, was obtained. Immunological results showed that the serum specific antibody level in the vaccinated group reached 1×104 after three immunizations. The proportion of CD4+T cells and CD4/CD8 cells was significantly higher (P<0.05) in the vaccinated groups than the blank control group. Further, cytokine (TNF-α) secretion decreased in the aluminum adjuvant and Pickering emulsion groups but increased in the Freund's adjuvant group. All three vaccinated groups of mice exhibited low but detectable levels of IFN-γ secretion.

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