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dc.contributor.authorMcCoy, Laura E.
dc.contributor.authorvan Gils, Marit J.
dc.contributor.authorOzorowski, Gabriel
dc.contributor.authorMessmer, Terrence
dc.contributor.authorBriney, Bryan
dc.contributor.authorVoss, James E.
dc.contributor.authorKulp, Daniel W.
dc.contributor.authorMacauley, Matthew S.
dc.contributor.authorSok, Devin
dc.contributor.authorPauthner, Matthias
dc.contributor.authorMenis, Sergey
dc.contributor.authorCottrell, Christopher A.
dc.contributor.authorTorres, Jonathan L.
dc.contributor.authorHsueh, Jessica
dc.contributor.authorSchief, William R.
dc.contributor.authorWilson, Ian A.
dc.contributor.authorWard, Andrew B.
dc.contributor.authorSanders, Rogier W.
dc.contributor.authorBurton, Dennis R.
dc.date.accessioned2016-10-24T15:46:54Z
dc.date.available2016-10-24T15:46:54Z
dc.date.issued2016-08
dc.identifier.issn22111247
dc.identifier.urihttp://hdl.handle.net/1721.1/104939
dc.description.abstractA major advance in the search for an HIV vaccine has been the development of a near-native Envelope trimer (BG505 SOSIP.664) that can induce robust autologous Tier 2 neutralization. Here, potently neutralizing monoclonal antibodies (nAbs) from rabbits immunized with BG505 SOSIP.664 are shown to recognize an immunodominant region of gp120 centered on residue 241. Residue 241 occupies a hole in the glycan defenses of the BG505 isolate, with fewer than 3% of global isolates lacking a glycan site at this position. However, at least one conserved glycan site is missing in 89% of viruses, suggesting the presence of glycan holes in most HIV isolates. Serum evidence is consistent with targeting of holes in natural infection. The immunogenic nature of breaches in the glycan shield has been under-appreciated in previous attempts to understand autologous neutralizing antibody responses and has important potential consequences for HIV vaccine design.en_US
dc.description.sponsorshipInternational AIDS Vaccine Initiative. Neutralizing Antibody Consortium. (Collaboration for AIDS Vaccine Discovery Grants OPP1084519 and OPP1115782)en_US
dc.description.sponsorshipDuke Center for HIV/AIDS Vaccine Immunology and Immunogen (Discovery Grant UM1AI100663)en_US
dc.description.sponsorshipUnited States. Agency for International Developmenten_US
dc.description.sponsorshipBill & Melinda Gates Foundationen_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.celrep.2016.07.074en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourceCell Reportsen_US
dc.titleHoles in the Glycan Shield of the Native HIV Envelope Are a Target of Trimer-Elicited Neutralizing Antibodiesen_US
dc.typeArticleen_US
dc.identifier.citationMcCoy, Laura E. et al. “Holes in the Glycan Shield of the Native HIV Envelope Are a Target of Trimer-Elicited Neutralizing Antibodies.” Cell Reports 16.9 (2016): 2327–2338.en_US
dc.contributor.departmentRagon Institute of MGH, MIT and Harvarden_US
dc.contributor.mitauthorBurton, Dennis R.
dc.relation.journalCell Reportsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsMcCoy, Laura E.; van Gils, Marit J.; Ozorowski, Gabriel; Messmer, Terrence; Briney, Bryan; Voss, James E.; Kulp, Daniel W.; Macauley, Matthew S.; Sok, Devin; Pauthner, Matthias; Menis, Sergey; Cottrell, Christopher A.; Torres, Jonathan L.; Hsueh, Jessica; Schief, William R.; Wilson, Ian A.; Ward, Andrew B.; Sanders, Rogier W.; Burton, Dennis R.en_US
dspace.embargo.termsNen_US
mit.licensePUBLISHER_CCen_US


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