| Literature DB >> 28381540 |
Chad E Mire1,2, Joan B Geisbert1,2, Viktoriya Borisevich1,2, Karla A Fenton1,2, Krystle N Agans1,2, Andrew I Flyak3, Daniel J Deer1,2, Herta Steinkellner4, Ognian Bohorov5, Natasha Bohorova5, Charles Goodman5, Andrew Hiatt5, Do H Kim5, Michael H Pauly5, Jesus Velasco5, Kevin J Whaley4, James E Crowe3,6,7, Larry Zeitlin8, Thomas W Geisbert9,2.
Abstract
As observed during the 2013-2016 Ebola virus disease epidemic, containment of filovirus outbreaks is challenging and made more difficult by the lack of approved vaccine or therapeutic options. Marburg and Ravn viruses are highly virulent and cause severe and frequently lethal disease in humans. Monoclonal antibodies (mAbs) are a platform technology in wide use for autoimmune and oncology indications. Previously, we described human mAbs that can protect mice from lethal challenge with Marburg virus. We demonstrate that one of these mAbs, MR191-N, can confer a survival benefit of up to 100% to Marburg or Ravn virus-infected rhesus macaques when treatment is initiated up to 5 days post-inoculation. These findings extend the small but growing body of evidence that mAbs can impart therapeutic benefit during advanced stages of disease with highly virulent viruses and could be useful in epidemic settings.Entities:
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Year: 2017 PMID: 28381540 PMCID: PMC5719873 DOI: 10.1126/scitranslmed.aai8711
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956