Please use this identifier to cite or link to this item: https://doi.org/10.1038/nbt1332
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dc.titleExploiting lymphatic transport and complement activation in nanoparticle vaccines
dc.contributor.authorReddy, S.T.
dc.contributor.authorVan Der Vlies, A.J.
dc.contributor.authorSimeoni, E.
dc.contributor.authorAngeli, V.
dc.contributor.authorRandolph, G.J.
dc.contributor.authorO'Neil, C.P.
dc.contributor.authorLee, L.K.
dc.contributor.authorSwartz, M.A.
dc.contributor.authorHubbell, J.A.
dc.date.accessioned2016-11-29T01:19:51Z
dc.date.available2016-11-29T01:19:51Z
dc.date.issued2007-10
dc.identifier.citationReddy, S.T., Van Der Vlies, A.J., Simeoni, E., Angeli, V., Randolph, G.J., O'Neil, C.P., Lee, L.K., Swartz, M.A., Hubbell, J.A. (2007-10). Exploiting lymphatic transport and complement activation in nanoparticle vaccines. Nature Biotechnology 25 (10) : 1159-1164. ScholarBank@NUS Repository. https://doi.org/10.1038/nbt1332
dc.identifier.issn10870156
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/131541
dc.description.abstractAntigen targeting and adjuvancy schemes that respectively facilitate delivery of antigen to dendritic cells and elicit their activation have been explored in vaccine development. Here we investigate whether nanoparticles can be used as a vaccine platform by targeting lymph node-residing dendritic cells via interstitial flow and activating these cells by in situ complement activation. After intradermal injection, interstitial flow transported ultra-small nanoparticles (25 nm) highly efficiently into lymphatic capillaries and their draining lymph nodes, targeting half of the lymph node-residing dendritic cells, whereas 100-nm nanoparticles were only 10% as efficient. The surface chemistry of these nanoparticles activated the complement cascade, generating a danger signal in situ and potently activating dendritic cells. Using nanoparticles conjugated to the model antigen ovalbumin, we demonstrate generation of humoral and cellular immunity in mice in a size- and complement-dependent manner. © 2007 Nature Publishing Group.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1038/nbt1332
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentMICROBIOLOGY
dc.description.doi10.1038/nbt1332
dc.description.sourcetitleNature Biotechnology
dc.description.volume25
dc.description.issue10
dc.description.page1159-1164
dc.description.codenNABIF
dc.identifier.isiut000250226600027
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