免疫系统
抗原
免疫
接种疫苗
病毒学
免疫学
抗体
鼻腔给药
疫苗效力
医学
生物
作者
Tong Ye,Zhouguang Jiao,Xin Li,Zhanlong He,Yanyan Li,Fengmei Yang,Xin Zhao,Youchun Wang,Weijin Huang,Meng Qin,Yingmei Feng,Yefeng Qiu,Wenhui Yang,Lingfei Hu,Yaling Hu,Yu Zhai,Erqiang Wang,Di Yu,Shuang Wang,Hua Yue
出处
期刊:Nature
[Springer Nature]
日期:2023-12-13
卷期号:624 (7992): 630-638
被引量:120
标识
DOI:10.1038/s41586-023-06809-8
摘要
The COVID-19 pandemic has fostered major advances in vaccination technologies1-4; however, there are urgent needs for vaccines that induce mucosal immune responses and for single-dose, non-invasive administration4-6. Here we develop an inhalable, single-dose, dry powder aerosol SARS-CoV-2 vaccine that induces potent systemic and mucosal immune responses. The vaccine encapsulates assembled nanoparticles comprising proteinaceous cholera toxin B subunits displaying the SARS-CoV-2 RBD antigen within microcapsules of optimal aerodynamic size, and this unique nano-micro coupled structure supports efficient alveoli delivery, sustained antigen release and antigen-presenting cell uptake, which are favourable features for the induction of immune responses. Moreover, this vaccine induces strong production of IgG and IgA, as well as a local T cell response, collectively conferring effective protection against SARS-CoV-2 in mice, hamsters and nonhuman primates. Finally, we also demonstrate a mosaic iteration of the vaccine that co-displays ancestral and Omicron antigens, extending the breadth of antibody response against co-circulating strains and transmission of the Omicron variant. These findings support the use of this inhaled vaccine as a promising multivalent platform for fighting COVID-19 and other respiratory infectious diseases.
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