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Abstract 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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Man Xing
Tianjin Medical University
Gaowei Hu
Qingdao Institute of Marine Geology
Xiang Wang
Shanghai Public Health Clinical Center
npj Vaccines
Shanghai Medical College of Fudan University
Tianjin Medical University
Shanghai Public Health Clinical Center
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Xing et al. (Thu,) studied this question.
synapsesocial.com/papers/68e72f63b6db6435876a926e — DOI: https://doi.org/10.1038/s41541-024-00857-5