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dc.contributor.authorKim, Seong A.-
dc.contributor.authorLee, Yeram-
dc.contributor.authorKo, Yeju-
dc.contributor.authorKim, Seohyun-
dc.contributor.authorKim, Gi Beom-
dc.contributor.authorLee, Na Kyeong-
dc.contributor.authorAhn, Wonkyung-
dc.contributor.authorKim, Nayeon-
dc.contributor.authorNam, Gi-Hoon-
dc.contributor.authorLee, Eun Jung-
dc.contributor.authorKim, In-San-
dc.date.accessioned2024-01-19T10:30:44Z-
dc.date.available2024-01-19T10:30:44Z-
dc.date.created2023-02-10-
dc.date.issued2023-01-
dc.identifier.issn0168-3659-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/114131-
dc.description.abstractProtein nanocages have attracted considerable attention in various fields of nanomedicine due to their intrinsic properties, including biocompatibility, biodegradability, high structural stability, and ease of modification of their surfaces and inner cavities. In vaccine development, these protein nanocages are suited for efficient tar-geting to and retention in the lymph nodes and can enhance immunogenicity through various mechanisms, including excellent uptake by antigen-presenting cells and crosslinking with multiple B cell receptors. This re-view highlights the superiority of protein nanocages as antigen delivery carriers based on their physiological and immunological properties such as biodistribution, immunogenicity, stability, and multifunctionality. With a focus on design, we discuss the utilization and efficacy of protein nanocages such as virus-like particles, caged proteins, and artificial caged proteins against cancer and infectious diseases such as coronavirus disease 2019 (COVID-19). In addition, we summarize available knowledge on the protein nanocages that are currently used in clinical trials and provide a general outlook on conventional distribution techniques and hurdles faced, partic-ularly for therapeutic cancer vaccines.-
dc.languageEnglish-
dc.publisherElsevier BV-
dc.titleProtein-based nanocages for vaccine development-
dc.typeArticle-
dc.identifier.doi10.1016/j.jconrel.2022.12.022-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJournal of Controlled Release, v.353, pp.767 - 791-
dc.citation.titleJournal of Controlled Release-
dc.citation.volume353-
dc.citation.startPage767-
dc.citation.endPage791-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000915247500001-
dc.identifier.scopusid2-s2.0-85144309167-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.type.docTypeArticle-
dc.subject.keywordPlusVIRUS-LIKE PARTICLES-
dc.subject.keywordPlusHEAT-SHOCK-PROTEIN-
dc.subject.keywordPlusNEUTRALIZING ANTIBODY-RESPONSES-
dc.subject.keywordPlusORIGINAL ANTIGENIC SIN-
dc.subject.keywordPlusIN-SITU VACCINATION-
dc.subject.keywordPlusMOSAIC-VIRUS-
dc.subject.keywordPlusNANOPARTICLE VACCINES-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusPROTECTIVE IMMUNITY-
dc.subject.keywordPlusFERRITIN NANOCAGE-
dc.subject.keywordAuthorProtein nanocage-
dc.subject.keywordAuthorVirus -like particle-
dc.subject.keywordAuthorVaccine-
dc.subject.keywordAuthorCancer vaccine-
dc.subject.keywordAuthorSARS-CoV-2-
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KIST Article > 2023
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