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dc.contributor.authorJi, Wangen_US
dc.contributor.authorShah, Dilipen_US
dc.contributor.authorChen, Xinyuanen_US
dc.contributor.authorAnderson, R. Roxen_US
dc.contributor.authorWu, Mei X.en_US
dc.date.accessioned2015-05-04T15:27:28Z
dc.date.issued2015en_US
dc.identifier.citationJi, Wang, Dilip Shah, Xinyuan Chen, R. Rox Anderson, and Mei X. Wu. 2015. “A micro-sterile inflammation array as an adjuvant for influenza vaccines.” Nature communications 5 (1): 4447. doi:10.1038/ncomms5447. http://dx.doi.org/10.1038/ncomms5447.en
dc.identifier.issn2041-1723en
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:15034938
dc.description.abstractThere is an urgent need of adjuvants for cutaneous vaccination. Here we report that micro-sterile inflammation induced at inoculation sites can augment immune responses to influenza vaccines in animal models. The inoculation site is briefly illuminated with a handheld, non-ablative fractional laser before the vaccine is intradermally administered, which creates an array of self-healing microthermal zones (MTZs) in the skin. The dying cells in the MTZs send “danger” signals that attract a large number of antigen-presenting cells, in particular, plasmacytoid dendritic cells (pDCs) around each MTZ forming a micro-sterile inflammation array. A pivotal role for pDCs in the adjuvanticity is ascertained by significant abrogation of the immunity after systemic depletion of pDCs, local application of a TNF-α inhibitor, or null mutation of IFN regulatory factor7 (IRF7). In contrast to conventional adjuvants that cause persistent inflammation and skin lesions, micro-sterile inflammation enhances efficacy of influenza vaccines, yet with diminished adverse effects.en
dc.language.isoen_USen
dc.relation.isversionofdoi:10.1038/ncomms5447en
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC4391636/pdf/en
dash.licenseLAAen_US
dc.titleA micro-sterile inflammation array as an adjuvant for influenza vaccinesen
dc.typeJournal Articleen_US
dc.description.versionVersion of Recorden
dc.relation.journalNature communicationsen
dash.depositing.authorWu, Mei X.en_US
dc.date.available2015-05-04T15:27:28Z
dc.identifier.doi10.1038/ncomms5447*
dash.contributor.affiliatedWu, Mei


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