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dc.contributor.authorIrvine, Darrell
dc.date.accessioned2023-02-23T18:52:53Z
dc.date.available2023-02-23T18:52:53Z
dc.date.issued2022
dc.identifier.urihttps://hdl.handle.net/1721.1/148202
dc.description.abstractActivation of the innate immune system via pattern recognition receptors (PRRs) is key to generate lasting adaptive immunity. PRRs detect unique chemical patterns associated with invading microorganisms, but whether and how the physical properties of PRR ligands influence the development of the immune response remains unknown. Through the study of fungal mannans, we show that the physical form of PRR ligands dictates the immune response. Soluble mannans are immunosilent in the periphery but elicit a potent pro-inflammatory response in the draining lymph node (dLN). By modulating the physical form of mannans, we developed a formulation that targets both the periphery and the dLN. When combined with viral glycoprotein antigens, this mannan formulation broadens epitope recognition, elicits potent antigen-specific neutralizing antibodies, and confers protection against viral infections of the lung. Thus, the physical properties of microbial ligands determine the outcome of the immune response and can be harnessed for vaccine development.en_US
dc.language.isoen
dc.publisherElsevier BVen_US
dc.relation.isversionof10.1016/J.CELL.2022.01.009en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titleAn adjuvant strategy enabled by modulation of the physical properties of microbial ligands expands antigen immunogenicityen_US
dc.typeArticleen_US
dc.identifier.citationIrvine, Darrell. 2022. "An adjuvant strategy enabled by modulation of the physical properties of microbial ligands expands antigen immunogenicity." Cell, 185 (4).
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineering
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineering
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MIT
dc.contributor.departmentRagon Institute of MGH, MIT and Harvard
dc.contributor.departmentHoward Hughes Medical Institute
dc.relation.journalCellen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2023-02-23T18:44:53Z
dspace.orderedauthorsBorriello, F; Poli, V; Shrock, E; Spreafico, R; Liu, X; Pishesha, N; Carpenet, C; Chou, J; Di Gioia, M; McGrath, ME; Dillen, CA; Barrett, NA; Lacanfora, L; Franco, ME; Marongiu, L; Iwakura, Y; Pucci, F; Kruppa, MD; Ma, Z; Lowman, DW; Ensley, HE; Nanishi, E; Saito, Y; O’Meara, TR; Seo, H-S; Dhe-Paganon, S; Dowling, DJ; Frieman, M; Elledge, SJ; Levy, O; Irvine, DJ; Ploegh, HL; Williams, DL; Zanoni, Ien_US
dspace.date.submission2023-02-23T18:45:04Z
mit.journal.volume185en_US
mit.journal.issue4en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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