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Article: An RNA-Scaffold Protein Subunit Vaccine for Nasal Immunization

TitleAn RNA-Scaffold Protein Subunit Vaccine for Nasal Immunization
Authors
Keywordsmucosal immunity
nasal vaccine
protein subunit vaccine
RNA scaffold
SARS-CoV-2
self-adjuvanted
Issue Date29-Sep-2023
PublisherMultidisciplinary Digital Publishing Institute (MDPI)
Citation
Vaccines, 2023, v. 11, n. 10 How to Cite?
AbstractDeveloping recombinant proteins as nasal vaccines for inducing systemic and mucosal immunity against respiratory viruses is promising. However, additional adjuvants are required to overcome the low immunogenicity of protein antigens. Here, a self-adjuvanted protein-RNA ribonucleoprotein vaccine was developed and found to be an effective nasal vaccine in mice and the SARS-CoV-2 infection model. The vaccine consisted of spike RBD (as an antigen), nucleoprotein (as an adaptor), and ssRNA (as an adjuvant and RNA scaffold). This combination robustly induced mucosal IgA, neutralizing antibodies and activated multifunctional T-cells, while also providing sterilizing immunity against live virus challenge. In addition, high-resolution scRNA-seq analysis highlighted airway-resident immune cells profile during prime-boost immunization. The vaccine also possesses modularity (antigen/adaptor/RNA scaffold) and can be made to target other viruses. This protein-RNA ribonucleoprotein vaccine is a novel and promising approach for developing safe and potent nasal vaccines to combat respiratory virus infections.
Persistent Identifierhttp://hdl.handle.net/10722/347643
ISSN
2023 Impact Factor: 5.2
2023 SCImago Journal Rankings: 1.201

 

DC FieldValueLanguage
dc.contributor.authorLam, Joy Yan-
dc.contributor.authorWong, Wan Man-
dc.contributor.authorYuen, Chun Kit-
dc.contributor.authorNg, Yau Yee-
dc.contributor.authorSan, Chun Hin-
dc.contributor.authorYuen, Kwok Yung-
dc.contributor.authorKok, Kin Hang-
dc.date.accessioned2024-09-26T00:30:20Z-
dc.date.available2024-09-26T00:30:20Z-
dc.date.issued2023-09-29-
dc.identifier.citationVaccines, 2023, v. 11, n. 10-
dc.identifier.issn2076-393X-
dc.identifier.urihttp://hdl.handle.net/10722/347643-
dc.description.abstractDeveloping recombinant proteins as nasal vaccines for inducing systemic and mucosal immunity against respiratory viruses is promising. However, additional adjuvants are required to overcome the low immunogenicity of protein antigens. Here, a self-adjuvanted protein-RNA ribonucleoprotein vaccine was developed and found to be an effective nasal vaccine in mice and the SARS-CoV-2 infection model. The vaccine consisted of spike RBD (as an antigen), nucleoprotein (as an adaptor), and ssRNA (as an adjuvant and RNA scaffold). This combination robustly induced mucosal IgA, neutralizing antibodies and activated multifunctional T-cells, while also providing sterilizing immunity against live virus challenge. In addition, high-resolution scRNA-seq analysis highlighted airway-resident immune cells profile during prime-boost immunization. The vaccine also possesses modularity (antigen/adaptor/RNA scaffold) and can be made to target other viruses. This protein-RNA ribonucleoprotein vaccine is a novel and promising approach for developing safe and potent nasal vaccines to combat respiratory virus infections.-
dc.languageeng-
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)-
dc.relation.ispartofVaccines-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectmucosal immunity-
dc.subjectnasal vaccine-
dc.subjectprotein subunit vaccine-
dc.subjectRNA scaffold-
dc.subjectSARS-CoV-2-
dc.subjectself-adjuvanted-
dc.titleAn RNA-Scaffold Protein Subunit Vaccine for Nasal Immunization -
dc.typeArticle-
dc.identifier.doi10.3390/vaccines11101550-
dc.identifier.scopuseid_2-s2.0-85175312371-
dc.identifier.volume11-
dc.identifier.issue10-
dc.identifier.issnl2076-393X-

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