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dc.contributor.authorTharakaraman, Kannan
dc.contributor.authorSubramanian, Vidya
dc.contributor.authorCain, David
dc.contributor.authorSasisekharan, Viswanathan
dc.contributor.authorSasisekharan, Ram
dc.date.accessioned2015-10-29T18:54:31Z
dc.date.available2015-10-29T18:54:31Z
dc.date.issued2014-05
dc.date.submitted2014-04
dc.identifier.issn19313128
dc.identifier.urihttp://hdl.handle.net/1721.1/99522
dc.description.abstractBroadly neutralizing antibodies (bNAb) that target a conserved region of a viral antigen hold significant therapeutic promise. CR8020 is a bNAb that targets the stem region of influenza A virus (IAV) hemagglutinin (HA). CR8020 is currently being evaluated for prophylactic use against group 2 IAVs in phase II studies. Structural and computational analyses reported here indicate that CR8020 targets HA residues that are prone to antigenic drift and host selection pressure. Critically, CR8020 escape mutation is seen in certain H7N9 viruses from recent outbreaks. Furthermore, the ability of the bNAb Fc region to effectively engage activating Fcγ receptors (FCγR) is essential for antibody efficacy. In this regard, our data indicate that the membrane could sterically hinder the formation of HA-CR8020-FcγRIIa/HA-IgG-FcγRIIIa ternary complexes. Altogether, our analyses suggest that epitope mutability and accessibility to immune complex assembly are important attributes to consider when evaluating bNAb candidates for clinical development.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Merit Award R37 GM057073-13)en_US
dc.description.sponsorshipSingapore. National Research Foundation (Singapore-MIT Alliance for Research and Technology)en_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.chom.2014.04.009en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titleBroadly Neutralizing Influenza Hemagglutinin Stem-Specific Antibody CR8020 Targets Residues that Are Prone to Escape due to Host Selection Pressureen_US
dc.typeArticleen_US
dc.identifier.citationTharakaraman, Kannan, Vidya Subramanian, David Cain, Viswanathan Sasisekharan, and Ram Sasisekharan. “Broadly Neutralizing Influenza Hemagglutinin Stem-Specific Antibody CR8020 Targets Residues That Are Prone to Escape Due to Host Selection Pressure.” Cell Host & Microbe 15, no. 5 (May 2014): 644–651.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. School of Engineeringen_US
dc.contributor.departmentMIT Skoltech Initiativeen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorTharakaraman, Kannanen_US
dc.contributor.mitauthorSubramanian, Vidyaen_US
dc.contributor.mitauthorCain, Daviden_US
dc.contributor.mitauthorSasisekharan, Viswanathanen_US
dc.contributor.mitauthorSasisekharan, Ramen_US
dc.relation.journalCell Host & Microbeen_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
dspace.orderedauthorsTharakaraman, Kannan; Subramanian, Vidya; Cain, David; Sasisekharan, Viswanathan; Sasisekharan, Ramen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-2085-7840
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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