Show simple item record

dc.contributor.authorRider, Todd H.
dc.contributor.authorZook, Christina E.
dc.contributor.authorBoettcher, Tara L.
dc.contributor.authorWick, Scott T.
dc.contributor.authorPancoast, Jennifer S.
dc.contributor.authorZusman, Benjamin D.
dc.date.accessioned2011-10-13T14:08:56Z
dc.date.available2011-10-13T14:08:56Z
dc.date.issued2011-07
dc.date.submitted2011-05
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/1721.1/66234
dc.description.abstractCurrently there are relatively few antiviral therapeutics, and most which do exist are highly pathogen-specific or have other disadvantages. We have developed a new broad-spectrum antiviral approach, dubbed Double-stranded RNA (dsRNA) Activated Caspase Oligomerizer (DRACO) that selectively induces apoptosis in cells containing viral dsRNA, rapidly killing infected cells without harming uninfected cells. We have created DRACOs and shown that they are nontoxic in 11 mammalian cell types and effective against 15 different viruses, including dengue flavivirus, Amapari and Tacaribe arenaviruses, Guama bunyavirus, and H1N1 influenza. We have also demonstrated that DRACOs can rescue mice challenged with H1N1 influenza. DRACOs have the potential to be effective therapeutics or prophylactics for numerous clinical and priority viruses, due to the broad-spectrum sensitivity of the dsRNA detection domain, the potent activity of the apoptosis induction domain, and the novel direct linkage between the two which viruses have never encountered.en_US
dc.description.sponsorshipNational Institute of Allergy and Infectious Diseases (U.S.) (grant AI057159)en_US
dc.description.sponsorshipNew England Regional Center of Excellence for Biodefense and Emerging Infectious Diseasesen_US
dc.description.sponsorshipUnited States. Dept. of Defense (Director of Defense Research & Engineering)en_US
dc.description.sponsorshipUnited States. Defense Threat Reduction Agencyen_US
dc.description.sponsorshipUnited States. Defense Advanced Research Projects Agencyen_US
dc.language.isoen_US
dc.publisherPublic Library of Scienceen_US
dc.relation.isversionofhttp://dx.doi.org/10.1371/journal.pone.0022572en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/en_US
dc.sourcePLoSen_US
dc.titleBroad-Spectrum Antiviral Therapeuticsen_US
dc.typeArticleen_US
dc.identifier.citationRider, Todd H. et al. “Broad-Spectrum Antiviral Therapeutics.” Ed. Suryaprakash Sambhara. PLoS ONE 6 (2011): e22572.en_US
dc.contributor.departmentLincoln Laboratoryen_US
dc.contributor.approverRider, Todd H.
dc.contributor.mitauthorRider, Todd H.
dc.contributor.mitauthorZook, Christina E.
dc.contributor.mitauthorBoettcher, Tara L.
dc.contributor.mitauthorWick, Scott T.
dc.contributor.mitauthorPancoast, Jennifer S.
dc.contributor.mitauthorZusman, Benjamin D.
dc.relation.journalPLoS ONEen_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.orderedauthorsRider, Todd H.; Zook, Christina E.; Boettcher, Tara L.; Wick, Scott T.; Pancoast, Jennifer S.; Zusman, Benjamin D.en
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record