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dc.contributor.authorTharakaraman, Kannan
dc.contributor.authorSubramanian, Vidya
dc.contributor.authorViswanathan, Karthik
dc.contributor.authorSloan, Susan
dc.contributor.authorYen, Hui-Ling
dc.contributor.authorBarnard, Dale L.
dc.contributor.authorLeung, Y. H. Connie
dc.contributor.authorSzretter, Kristy J.
dc.contributor.authorKoch, Tyree J.
dc.contributor.authorDelaney, James C.
dc.contributor.authorBabcock, Gregory J.
dc.contributor.authorSasisekharan, Ram
dc.contributor.authorShriver, Zachary
dc.contributor.authorWogan, Gerald N
dc.date.accessioned2016-04-04T17:15:51Z
dc.date.available2016-04-04T17:15:51Z
dc.date.issued2015-09
dc.date.submitted2014-11
dc.identifier.issn0027-8424
dc.identifier.issn1091-6490
dc.identifier.urihttp://hdl.handle.net/1721.1/102129
dc.description.abstractEmerging strains of influenza represent a significant public health threat with potential pandemic consequences. Of particular concern are the recently emerged H7N9 strains which cause pneumonia with acute respiratory distress syndrome. Estimates are that nearly 80% of hospitalized patients with H7N9 have received intensive care unit support. VIS410, a human antibody, targets a unique conserved epitope on influenza A. We evaluated the efficacy of VIS410 for neutralization of group 2 influenza strains, including H3N2 and H7N9 strains in vitro and in vivo. VIS410, administered at 50 mg/kg, protected DBA mice infected with A/Anhui/2013 (H7N9), resulting in significant survival benefit upon single-dose (−24 h) or double-dose (−12 h, +48 h) administration (P < 0.001). A single dose of VIS410 at 50 mg/kg (−12 h) combined with oseltamivir at 50 mg/kg (−12 h, twice daily for 7 d) in C57BL/6 mice infected with A/Shanghai 2/2013 (H7N9) resulted in significant decreased lung viral load (P = 0.002) and decreased lung cytokine responses for nine of the 11 cytokines measured. Based on these results, we find that VIS410 may be effective either as monotherapy or combined with antivirals in treating H7N9 disease, as well as disease from other influenza strains.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.publisherNational Academy of Sciences (U.S.)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1073/pnas.1502374112en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceNational Academy of Sciences (U.S.)en_US
dc.titleA broadly neutralizing human monoclonal antibody is effective against H7N9en_US
dc.typeArticleen_US
dc.identifier.citationTharakaraman, Kannan, Vidya Subramanian, Karthik Viswanathan, Susan Sloan, Hui-Ling Yen, Dale L. Barnard, Y. H. Connie Leung, et al. “A Broadly Neutralizing Human Monoclonal Antibody Is Effective Against H7N9.” Proc Natl Acad Sci USA 112, no. 35 (August 17, 2015): 10890–10895.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.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorTharakaraman, Kannanen_US
dc.contributor.mitauthorSubramanian, Vidyaen_US
dc.contributor.mitauthorWogan, Gerald N.en_US
dc.contributor.mitauthorSasisekharan, Ramen_US
dc.relation.journalProceedings of the National Academy of Sciencesen_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.orderedauthorsTharakaraman, Kannan; Subramanian, Vidya; Viswanathan, Karthik; Sloan, Susan; Yen, Hui-Ling; Barnard, Dale L.; Leung, Y. H. Connie; Szretter, Kristy J.; Koch, Tyree J.; Delaney, James C.; Babcock, Gregory J.; Wogan, Gerald N.; Sasisekharan, Ram; Shriver, Zacharyen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-2085-7840
dc.identifier.orcidhttps://orcid.org/0000-0003-0771-9889
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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