Successful post-exposure prophylaxis of Ebola infected non-human primates using Ebola glycoprotein-specific equine IgG

نویسندگان

  • Oleg V. Pyankov
  • Yin Xiang Setoh
  • Sergey A. Bodnev
  • Judith H. Edmonds
  • Olga G. Pyankova
  • Stepan A. Pyankov
  • Gabor Pali
  • Shane Belford
  • Louis Lu
  • Mylinh La
  • George Lovrecz
  • Valentina A. Volchkova
  • Keith J. Chappell
  • Daniel Watterson
  • Glenn Marsh
  • Paul R. Young
  • Alexander A. Agafonov
  • Jillann F. Farmer
  • Victor E. Volchkov
  • Andreas Suhrbier
  • Alexander A. Khromykh
چکیده

Herein we describe production of purified equine IgG obtained from horses immunized with plasmid DNA followed by boosting with Kunjin replicon virus-like particles both encoding a modified Ebola glycoprotein. Administration of the equine IgG over 5 days to cynomolgus macaques infected 24 hours previously with a lethal dose of Ebola virus suppressed viral loads by more than 5 logs and protected animals from mortality. Animals generated their own Ebola glycoprotein-specific IgG responses 9-15 days after infection, with circulating virus undetectable by day 15-17. Such equine IgG may find utility as a post-exposure prophylactic for Ebola infection and provides a low cost, scalable alternative to monoclonal antibodies, with extensive human safety data and WHO-standardized international manufacturing capability available in both high and low income countries.

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عنوان ژورنال:

دوره 7  شماره 

صفحات  -

تاریخ انتشار 2017