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Conference Paper: An intranasal influenza virus-vectored vaccine system for blocking SARS-CoV-2 and influenza virus infection

TitleAn intranasal influenza virus-vectored vaccine system for blocking SARS-CoV-2 and influenza virus infection
Authors
Issue Date16-Dec-2022
Abstract

We have developed an intranasal vaccine candidate based on a live attenuated influenza virus (LAIV) with a deleted NS1 gene that encodes cell surface expression of the receptor-binding-domain (RBD) of the SARS-CoV-2 spike protein, designated DelNS1-RBD LAIV. Immune responses and protection against SARS-CoV-2 variants challenge following intranasal administration of DeINS1-RBD vaccines were analyzed in animal models and compared with intramuscular injection of the mRNA vaccine. Notably, vaccination with DeINS1-RBD4N-DAF LAlVs, but not mRNA vaccine, blocked replication of SARS-CoV-2 variants, including Delta and Omicron variants, in the respiratory tissues of animals. A phased III study found DelNS1-RBD LAIV is highly safe and effective in humans. More importantly, DelNS1-RBD LAIV retain the full ability to induce immunity against influenza viruses. The DeINS1-RBD LAIV system is an ideal technology for creating dual function vaccines against both influenza and COVlD-19 for use In annual vaccination strategies.


Persistent Identifierhttp://hdl.handle.net/10722/337724

 

DC FieldValueLanguage
dc.contributor.authorChen, Honglin-
dc.date.accessioned2024-03-11T10:23:23Z-
dc.date.available2024-03-11T10:23:23Z-
dc.date.issued2022-12-16-
dc.identifier.urihttp://hdl.handle.net/10722/337724-
dc.description.abstract<p>We have developed an intranasal vaccine candidate based on a live attenuated influenza virus (LAIV) with a deleted NS1 gene that encodes cell surface expression of the receptor-binding-domain (RBD) of the SARS-CoV-2 spike protein, designated DelNS1-RBD LAIV. Immune responses and protection against SARS-CoV-2 variants challenge following intranasal administration of DeINS1-RBD vaccines were analyzed in animal models and compared with intramuscular injection of the mRNA vaccine. Notably, vaccination with DeINS1-RBD4N-DAF LAlVs, but not mRNA vaccine, blocked replication of SARS-CoV-2 variants, including Delta and Omicron variants, in the respiratory tissues of animals. A phased III study found DelNS1-RBD LAIV is highly safe and effective in humans. More importantly, DelNS1-RBD LAIV retain the full ability to induce immunity against influenza viruses. The DeINS1-RBD LAIV system is an ideal technology for creating dual function vaccines against both influenza and COVlD-19 for use In annual vaccination strategies.</p>-
dc.languageeng-
dc.relation.ispartof2nd Symposium on Combating Emerging Infectious Diseases (16/12/2022-16/12/2022, Hong Kong)-
dc.titleAn intranasal influenza virus-vectored vaccine system for blocking SARS-CoV-2 and influenza virus infection-
dc.typeConference_Paper-

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