College of Veterinary Medicine, Jiangsu Co-Innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou University, Yangzhou 225009, China.
Joint International Research Laboratory of Agriculture and Agri-Product Safety, The Ministry of Education of China, Yangzhou University, Yangzhou 225009, China.
Int J Mol Sci. 2024 Feb 9;25(4):2132. doi: 10.3390/ijms25042132.
H9N2 avian influenza poses a significant public health risk, necessitating effective vaccines for mass immunization. Oral inactivated vaccines offer advantages like the ease of administration, but their efficacy often requires enhancement through mucosal adjuvants. In a previous study, we established a novel complex of polysaccharide from Koidz binding with zinc oxide nanoparticles (AMP-ZnONPs) and preliminarily demonstrated its immune-enhancing function. This work aimed to evaluate the efficacy of AMP-ZnONPs as adjuvants in an oral H9N2-inactivated vaccine and the vaccine's impact on intestinal mucosal immunity. In this study, mice were orally vaccinated on days 0 and 14 after adapting to the environment. AMP-ZnONPs significantly improved HI titers, the levels of specific IgG, IgG1 and IgG2a in serum and sIgA in intestinal lavage fluid; increased the number of B-1 and B-2 cells and dendritic cell populations; and enhanced the mRNA expression of intestinal homing factors and immune-related cytokines. Interestingly, AMP-ZnONPs were more likely to affect B-1 cells than B-2 cells. AMP-ZnONPs showed mucosal immune enhancement that was comparable to positive control (cholera toxin, CT), but not to the side effect of weight loss caused by CT. Compared to the whole-inactivated H9N2 virus (WIV) group, the WIV + AMP-ZnONP and WIV + CT groups exhibited opposite shifts in gut microbial abundance. AMP-ZnONPs serve as an effective and safe mucosal adjuvant for oral WIV, improving cellular, humoral and mucosal immunity and microbiota in the gastrointestinal tract, avoiding the related undesired effects of CT.
H9N2 禽流感对公共健康构成重大威胁,因此需要有效的疫苗进行大规模免疫接种。口服灭活疫苗具有易于管理的优势,但它们的功效通常需要黏膜佐剂来增强。在之前的研究中,我们构建了一种新型多糖复合物,该复合物与氧化锌纳米粒子(AMP-ZnONPs)结合,并初步证明了其免疫增强功能。本研究旨在评估 AMP-ZnONPs 作为口服 H9N2 灭活疫苗佐剂的功效,以及该疫苗对肠道黏膜免疫的影响。在这项研究中,小鼠在适应环境后第 0 天和第 14 天经口接种疫苗。AMP-ZnONPs 显著提高了 HI 滴度、血清中特异性 IgG、IgG1 和 IgG2a 水平以及肠灌洗液中 sIgA 的水平;增加了 B-1 和 B-2 细胞以及树突状细胞群体的数量;并增强了肠道归巢因子和免疫相关细胞因子的 mRNA 表达。有趣的是,与 B-2 细胞相比,AMP-ZnONPs 更可能影响 B-1 细胞。AMP-ZnONPs 表现出黏膜免疫增强作用,与阳性对照(霍乱毒素,CT)相当,但不会引起 CT 导致的体重减轻等副作用。与全灭活 H9N2 病毒(WIV)组相比,WIV+AMP-ZnONP 和 WIV+CT 组的肠道微生物丰度发生了相反的变化。AMP-ZnONPs 作为口服 WIV 的有效且安全的黏膜佐剂,可改善细胞、体液和黏膜免疫以及胃肠道微生物群,避免 CT 相关的不良作用。