Xu Xiaohong, Qian Jing, Qin Lingsong, Li Jindou, Xue Cong, Ding Jiaxin, Wang Weiqi, Ding Wei, Yin Renfu, Jin Ningyi, Ding Zhuang
Laboratory of Infectious Diseases, College of Veterinary Medicine, Key Laboratory of Zoonosis Research, Ministry of Education, Jilin University, Changchun, 130062, China.
College of Basic Medical Science, Jilin University, Changchun, 130021, China.
Virol Sin. 2020 Aug;35(4):455-467. doi: 10.1007/s12250-020-00199-1. Epub 2020 Apr 9.
Newcastle disease virus (NDV) and H9N2 subtype Avian influenza virus (AIV) are two notorious avian respiratory pathogens that cause great losses in the poultry industry. Current inactivated commercial vaccines against NDV and AIV have the disadvantages of inadequate mucosal responses, while an attenuated live vaccine bears the risk of mutation. Dendritic cell (DC) targeting strategies are attractive for their potent mucosal and adaptive immune-stimulating ability against respiratory pathogens. In this study, DC-binding peptide (DCpep)-decorated chimeric virus-like particles (cVLPs), containing NDV haemagglutinin-neuraminidase (HN) and AIV haemagglutinin (HA), were developed as a DC-targeting mucosal vaccine candidate. DCpep-decorated cVLPs activated DCs in vitro, and induced potent immune stimulation in chickens, with enhanced secretory immunoglobulin A (sIgA) secretion and splenic T cell differentiation. 40 μg cVLPs can provide full protection against the challenge with homologous, heterologous NDV strains, and AIV H9N2. In addition, DCpep-decorated cVLPs could induce a better immune response when administered intranasally than intramuscularly, as indicated by robust sIgA secretion and a reduced virus shedding period. Taken together, this chimeric VLPs are a promising vaccine candidate to control NDV and AIV H9N2 and a useful platform bearing multivalent antigens.
新城疫病毒(NDV)和H9N2亚型禽流感病毒(AIV)是两种臭名昭著的禽类呼吸道病原体,给家禽业造成了巨大损失。目前针对NDV和AIV的灭活商业疫苗存在黏膜反应不足的缺点,而减毒活疫苗则有突变的风险。树突状细胞(DC)靶向策略因其对呼吸道病原体具有强大的黏膜和适应性免疫刺激能力而备受关注。在本研究中,开发了一种含有NDV血凝素-神经氨酸酶(HN)和AIV血凝素(HA)的、用DC结合肽(DCpep)修饰的嵌合病毒样颗粒(cVLPs)作为一种DC靶向黏膜疫苗候选物。用DCpep修饰的cVLPs在体外激活了DC,并在鸡体内诱导了强大的免疫刺激,增强了分泌型免疫球蛋白A(sIgA)的分泌和脾脏T细胞的分化。40μg cVLPs能够为抵御同源、异源NDV毒株以及AIV H9N2的攻击提供全面保护。此外,如强大的sIgA分泌和缩短的病毒排毒期所示,用DCpep修饰的cVLPs经鼻内给药时比经肌肉内给药能诱导更好的免疫反应。综上所述,这种嵌合VLPs是一种有前景的用于防控NDV和AIV H9N2的疫苗候选物,也是一个携带多价抗原的有用平台。