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AddaVax佐剂H5N8灭活疫苗可诱导针对不同H5病毒分支的强大体液免疫反应。

AddaVax-Adjuvanted H5N8 Inactivated Vaccine Induces Robust Humoral Immune Response against Different Clades of H5 Viruses.

作者信息

Gao Feixia, Liu Xueying, Dang Yudong, Duan Peng, Xu Wenting, Zhang Xin, Wang Shilei, Luo Jian, Li Xiuling

机构信息

Shanghai Institute of Biological Products, Shanghai 200052, China.

出版信息

Vaccines (Basel). 2022 Oct 9;10(10):1683. doi: 10.3390/vaccines10101683.

Abstract

Since some cases of human infections with H5N8 avian influenza virus have been reported and caused great concern in recent years, it is important to develop an effective vaccine for human use to prevent a potential H5N8 pandemic. In the present study, a vaccine candidate virus based on newly human-infected A/Astrakhan/3212/2020 H5N8 virus was constructed by reverse genetics (RG) technology. The immunogenicity of H5N8 whole virion inactivated vaccine was evaluated by various doses of vaccine antigen formulated with squalene-based adjuvant (AddaVax), aluminum hydroxide (Al(OH)) or without adjuvant in mice. The results showed AddaVax-adjuvanted H5N8 inactivated vaccine could stimulate the mice to produce a stronger protective immune response with higher titers of IgG antibodies, hemagglutination inhibition (HI), neuraminidase inhibition (NI) and microneutralization (MN) antibodies than vaccine formulations with Al(OH) adjuvant or without adjuvant, and achieve a dose-sparing effect. Moreover, the AddaVax-adjuvanted formulation also exhibited potent cross-reactive response in HI antibodies against different clades of H5 viruses. A significant correlation and a curve fitting among HI, NI and MN were found by the correlation analysis to predict the protective effect of the vaccine. With these findings, our study demonstrates that AddaVax adjuvant can enhance the immunogenicity of H5N8 inactivated vaccine remarkably, and proposes an effective strategy for dealing with a potential H5N8 virus pandemic.

摘要

近年来,由于已报告多例人类感染H5N8禽流感病毒的病例并引起了广泛关注,因此开发一种有效的人用疫苗以预防潜在的H5N8大流行至关重要。在本研究中,利用反向遗传学(RG)技术构建了一种基于新感染人类的A/阿斯特拉罕/3212/2020 H5N8病毒的候选疫苗病毒。通过用基于角鲨烯的佐剂(AddaVax)、氢氧化铝(Al(OH))配制不同剂量的疫苗抗原或在小鼠中不使用佐剂来评估H5N8全病毒灭活疫苗的免疫原性。结果表明,与使用Al(OH)佐剂或不使用佐剂的疫苗制剂相比,AddaVax佐剂的H5N8灭活疫苗能刺激小鼠产生更强的保护性免疫反应,产生更高滴度的IgG抗体、血凝抑制(HI)、神经氨酸酶抑制(NI)和微量中和(MN)抗体,并实现剂量节省效果。此外,AddaVax佐剂的制剂在HI抗体中也表现出对不同进化枝H5病毒的有效交叉反应。通过相关性分析发现HI、NI和MN之间存在显著相关性和曲线拟合,以预测疫苗的保护效果。基于这些发现,我们的研究表明AddaVax佐剂可显著增强H5N8灭活疫苗的免疫原性,并提出了应对潜在H5N8病毒大流行的有效策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fce/9612011/4cc581953ff6/vaccines-10-01683-g001.jpg

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