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

Identifieur interne : 001079 ( PubMed/Corpus ); précédent : 001078; suivant : 001080

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

Auteurs : 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

Source :

RBID : pubmed:28155869

Abstract

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.

DOI: 10.1038/srep41537
PubMed: 28155869

Links to Exploration step

pubmed:28155869

Le document en format XML

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<div type="abstract" xml:lang="en">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.</div>
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<CoiStatement>No competing financial interests for all authors. JFF is employed by the United Nations and views expressed herein are those of the author(s) and do not necessarily reflect the views of the United Nations.</CoiStatement>
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