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用于H9N2疫苗的阳离子纳米颗粒稳定疫苗递送系统,以促进鸡的免疫反应。

Cationic Nanoparticle-Stabilized Vaccine Delivery System for the H9N2 Vaccine to Promote Immune Response in Chickens.

作者信息

Zhang Yue, Zhu Tianyu, Xu Shuwen, Gu Pengfei, Cai Gaofeng, Peng Song, Liu Zhenguang, Yang Yang, Hu Yuanliang, Liu Jiaguo, Wang Deyun

机构信息

College of Veterinary Medicine, Institute of Traditional Chinese Veterinary Medicine, Nanjing, Jiangsu 210095, P. R. China.

MOE Joint International Research Laboratory of Animal Health and Food Safety, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, P. R. China.

出版信息

Mol Pharm. 2023 Mar 6;20(3):1613-1623. doi: 10.1021/acs.molpharmaceut.2c00805. Epub 2023 Feb 16.

Abstract

Chinese yam polysaccharides (CYPs) have received wide attention for their immunomodulatory activity. Our previous studies had discovered that the Chinese yam polysaccharide PLGA-stabilized Pickering emulsion (CYP-PPAS) can serve as an efficient adjuvant to trigger powerful humoral and cellular immunity. Recently, positively charged nano-adjuvants are easily taken up by antigen-presenting cells, potentially resulting in lysosomal escape, the promotion of antigen cross-presentation, and the induction of CD8 T-cell response. However, reports on the practical application of cationic Pickering emulsions as adjuvants are very limited. Considering the economic damage and public-health risks caused by the H9N2 influenza virus, it is urgent to develop an effective adjuvant for boosting humoral and cellular immunity against influenza virus infection. Here, we applied polyethyleneimine-modified Chinese yam polysaccharide PLGA nanoparticles as particle stabilizers and squalene as the oil core to fabricate a positively charged nanoparticle-stabilized Pickering emulsion adjuvant system (PEI-CYP-PPAS). The cationic Pickering emulsion of PEI-CYP-PPAS was utilized as an adjuvant for the H9N2 Avian influenza vaccine, and the adjuvant activity was compared with the Pickering emulsion of CYP-PPAS and the commercial adjuvant (aluminum adjuvant). The PEI-CYP-PPAS, with a size of about 1164.66 nm and a ζ potential of 33.23 mV, could increase the H9N2 antigen loading efficiency by 83.99%. After vaccination with Pickering emulsions based on H9N2 vaccines, PEI-CYP-PPAS generated higher HI titers and stronger IgG antibodies than CYP-PPAS and Alum and increased the immune organ index of the spleen and bursa of Fabricius without immune organ injury. Moreover, treatment with PEI-CYP-PPAS/H9N2 induced CD4 and CD8 T-cell activation, a high lymphocyte proliferation index, and increased cytokine expression of IL-4, IL-6, and IFN-γ. Thus, compared with the CYP-PPAS and aluminum adjuvant, the cationic nanoparticle-stabilized vaccine delivery system of PEI-CYP-PPAS was an effective adjuvant for H9N2 vaccination to elicit powerful humoral and cellular immune responses.

摘要

山药多糖(CYPs)因其免疫调节活性而受到广泛关注。我们之前的研究发现,山药多糖PLGA稳定的Pickering乳液(CYP-PPAS)可作为一种有效的佐剂,引发强大的体液免疫和细胞免疫。最近,带正电荷的纳米佐剂很容易被抗原呈递细胞摄取,可能导致溶酶体逃逸、促进抗原交叉呈递以及诱导CD8 T细胞反应。然而,关于阳离子Pickering乳液作为佐剂的实际应用的报道非常有限。考虑到H9N2流感病毒造成的经济损失和公共卫生风险,迫切需要开发一种有效的佐剂来增强针对流感病毒感染的体液免疫和细胞免疫。在此,我们应用聚乙烯亚胺修饰的山药多糖PLGA纳米颗粒作为颗粒稳定剂,角鲨烯作为油相核心,制备了一种带正电荷的纳米颗粒稳定的Pickering乳液佐剂系统(PEI-CYP-PPAS)。将PEI-CYP-PPAS的阳离子Pickering乳液用作H9N2禽流感疫苗的佐剂,并将其佐剂活性与CYP-PPAS的Pickering乳液和商业佐剂(铝佐剂)进行比较。PEI-CYP-PPAS的粒径约为1164.66 nm,ζ电位为33.23 mV,可使H9N2抗原负载效率提高83.99%。用基于H9N2疫苗的Pickering乳液接种后,PEI-CYP-PPAS产生的血凝抑制(HI)效价和IgG抗体比CYP-PPAS和铝佐剂更高,并且增加了脾脏和法氏囊的免疫器官指数,而没有免疫器官损伤。此外,PEI-CYP-PPAS/H9N2处理诱导了CD4和CD8 T细胞活化、高淋巴细胞增殖指数,并增加了IL-4、IL-6和IFN-γ的细胞因子表达。因此,与CYP-PPAS和铝佐剂相比,PEI-CYP-PPAS的阳离子纳米颗粒稳定的疫苗递送系统是一种有效的H9N2疫苗接种佐剂,可引发强大的体液免疫和细胞免疫反应。

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