Abstract |
As the world continues to experience the COVID-19 pandemic, seasonal influenza remain a cause of severe morbidity and mortality globally. Worse yet, coinfection with SARS-CoV-2 and influenza A virus (IAV) leads to more severe clinical outcomes. The development of a combined vaccine against both COVID-19 and influenza is thus of high priority. Based on our established lipid nanoparticle (LNP)-encapsulated mRNA vaccine platform, we developed and characterized a novel mRNA vaccine encoding the HA antigen of influenza A (H1N1) virus, termed ARIAV. Then, ARIAV was combined with our COVID-19 mRNA vaccine ARCoV, which encodes the receptor-binding domain (RBD) of the SARS-CoV-2 S protein, to formulate the final combined vaccine, AR-CoV/IAV. Further characterization demonstrated that immunization with two doses of AR-CoV/IAV elicited robust protective antibodies as well as antigen-specific cellular immune responses against SARS-CoV-2 and IAV. More importantly, AR-CoV/IAV immunization protected mice from coinfection with IAV and the SARS-CoV-2 Alpha and Delta variants. Our results highlight the potential of the LNP- mRNA vaccine platform in preventing COVID-19 and influenza, as well as other respiratory diseases.
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Authors | Qing Ye, Mei Wu, Chao Zhou, Xishan Lu, Baoying Huang, Ning Zhang, Hui Zhao, Hang Chi, Xiaojing Zhang, Dandan Ling, Rong-Rong Zhang, Zhuofan Li, Dan Luo, Yi-Jiao Huang, Hong-Ying Qiu, Haifeng Song, Wenjie Tan, Ke Xu, Bo Ying, Cheng-Feng Qin |
Journal | NPJ vaccines
(NPJ Vaccines)
Vol. 7
Issue 1
Pg. 84
(Jul 26 2022)
ISSN: 2059-0105 [Electronic] England |
PMID | 35882870
(Publication Type: Journal Article)
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Copyright | © 2022. The Author(s). |