An intranasal combination vaccine induces systemic and mucosal immunity against COVID-19 and influenza

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作者
Man Xing
Gaowei Hu
Xiang Wang
Yihan Wang
Furong He
Weiqian Dai
Xinyu Wang
Yixin Niu
Jiaojiao Liu
Hui Liu
Xiaoyan Zhang
Jianqing Xu
Qiliang Cai
Dongming Zhou
机构
[1] Tianjin Medical University,Department of Pathogen Biology, School of Basic Medical Sciences
[2] Fudan University,Shanghai Public Health Clinical Center
[3] Fudan University,MOE&NHC&CAMS Key Laboratory of Medical Molecular, Frontiers Science Center of Pathogenic Microorganisms and Infection, School of Basic Medical Sciences, Shanghai Medical College
[4] Fudan University,MOE&NHC&CAMS Key Laboratory of Medical Molecular Virology, Shanghai Institute of Infections Disease and Biosecurity, Frontiers Science Center of Pathogenic Microorganisms and Infection, School of Basic Medical Sciences, Shanghai Medical Co
[5] Ltd,Chengdu Kanghua Biological Products Co.
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npj Vaccines | / 9卷
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摘要
Despite prolonged surveillance and interventions, the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and influenza viruses continue to pose a severe global health burden. Thus, we developed a chimpanzee adenovirus-based combination vaccine, AdC68-HATRBD, with dual specificity against SARS-CoV-2 and influenza virus. When used as a standalone vaccine, intranasal immunization with AdC68-HATRBD induced comprehensive and potent immune responses consisting of immunoglobin (Ig) G, mucosal IgA, neutralizing antibodies, and memory T cells, which protected the mice from BA.5.2 and pandemic H1N1 infections. When used as a heterologous booster, AdC68-HATRBD markedly improved the protective immune response of the licensed SARS-CoV-2 or influenza vaccine. Therefore, whether administered intranasally as a standalone or booster vaccine, this combination vaccine is a valuable strategy to enhance the overall vaccine efficacy by inducing robust systemic and mucosal immune responses, thereby conferring dual lines of immunological defenses for these two viruses.
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