An intranasal combination vaccine induces systemic and mucosal immunity against COVID-19 and influenza.
Man XingGaowei HuXiang WangYihan WangFurong HeWeiqian DaiXinyu WangYixin NiuJiaojiao LiuHui LiuXiaoyan ZhangJianqing XuQiliang CaiDongming ZhouPublished in: NPJ vaccines (2024)
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.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- immune response
- coronavirus disease
- global health
- public health
- dendritic cells
- type diabetes
- drug induced
- diffusion weighted
- magnetic resonance imaging
- oxidative stress
- ulcerative colitis
- toll like receptor
- early onset
- magnetic resonance
- insulin resistance
- risk factors
- stress induced