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dc.contributor.authorNattika Nantachiten_US
dc.contributor.authorPanya Sunintaboonen_US
dc.contributor.authorSukathida Ubolen_US
dc.contributor.otherMahidol University. Faculty of Science. Department of Microbiologyen_US
dc.date.accessioned2017-08-09T04:57:35Z-
dc.date.available2017-08-09T04:57:35Z-
dc.date.created2017-08-09-
dc.date.issued2016-
dc.identifier.citationVirology Journal. Vol. 13, (2016), 142en_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/2744-
dc.description.abstractBackground: About half of the world’s population are living in the endemic area of dengue viruses implying that a rapid-mass vaccination may be required. In addition, a major target of dengue vaccine are children, thus, a needle-free administration is more attractive. These problems may be overcome by the alternative route of vaccination such as topical, oral and intranasal vaccination. Here, we investigated the possibility to deliver a dengue immunogen intranasally, a painless route of vaccination. The tested immunogen was the domain III of dengue serotype-3 E protein (EDIII-D3) loaded into trimethyl chitosan nanoparticles (EDIII-D3 TMC NPs). The primary human nasal epithelial cells, HNEpCs, were used as an in vitro model for nasal responses. Results: At tested concentrations, EDIII-D3 TMC NPs not only exerted no detectable toxicity toward HNEpC cultures but also efficiently delivered EDIII-D3 immunogens into HNEpCs. Moreover, HNEpCs quickly and strongly produced proinflammatory cytokines (IL-1β, IL-6, TNF-α), type-I IFN, the growth factors (GM-CSF, IL-7), the chemokines (MCP-1, MIP-1β, IL-8), Th1-related cytokines (IL-2, IL-12p70, IL-17, IFN-γ) and Th2-related cytokine (IL-4) in response to EDIII-D3 TMC NPs treatment. Conclusions: A potential mucosal delivery system for dengue immunogens was revealed and found to stimulate a strong local innate antiviral response which possibly leading to a systemic adaptive immunity.en_US
dc.language.isoenen_US
dc.rightsMahidol Universityen_US
dc.subjectOpen Access articleen_US
dc.subjectDomain III of dengue virusen_US
dc.subjectTrimethyl chitosan nanoparticlesen_US
dc.subjectNasal stimulationen_US
dc.subjectDengue vaccineen_US
dc.titleResponses of primary human nasal epithelial cells to EDIII-DENV stimulation: the first step to intranasal dengue vaccinationen_US
dc.typeResearch Articleen_US
dc.rights.holderBioMed Centralen_US
dc.identifier.doi10.1186/s12985-016-0598-z-
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