Your browser doesn't support javascript.
loading
Development of a Cost-effective Ovine Polyclonal Antibody-Based Product, EBOTAb, to Treat Ebola Virus Infection.
Dowall, Stuart David; Callan, Jo; Zeltina, Antra; Al-Abdulla, Ibrahim; Strecker, Thomas; Fehling, Sarah K; Krähling, Verena; Bosworth, Andrew; Rayner, Emma; Taylor, Irene; Charlton, Sue; Landon, John; Cameron, Ian; Hewson, Roger; Nasidi, Abdulsalami; Bowden, Thomas A; Carroll, Miles W.
Affiliation
  • Dowall SD; Public Health England, Salisbury.
  • Callan J; MicroPharm, Newcastle Emlyn.
  • Zeltina A; Division of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, United Kingdom.
  • Al-Abdulla I; MicroPharm, Newcastle Emlyn.
  • Strecker T; Institute of Virology, Philipps University Marburg, Germany.
  • Fehling SK; Institute of Virology, Philipps University Marburg, Germany.
  • Krähling V; Institute of Virology, Philipps University Marburg, Germany.
  • Bosworth A; Public Health England, Salisbury.
  • Rayner E; Public Health England, Salisbury.
  • Taylor I; Public Health England, Salisbury.
  • Charlton S; Public Health England, Salisbury.
  • Landon J; MicroPharm, Newcastle Emlyn.
  • Cameron I; MicroPharm, Newcastle Emlyn.
  • Hewson R; Public Health England, Salisbury.
  • Nasidi A; Nigerian Centre for Disease Control, Abuja.
  • Bowden TA; Division of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, United Kingdom.
  • Carroll MW; Public Health England, Salisbury.
J Infect Dis ; 213(7): 1124-33, 2016 Apr 01.
Article in En | MEDLINE | ID: mdl-26715676
ABSTRACT
The highly glycosylated glycoprotein spike of Ebola virus (EBOV-GP1,2) is the primary target of the humoral host response. Recombinant EBOV-GP ectodomain (EBOV-GP1,2ecto) expressed in mammalian cells was used to immunize sheep and elicited a robust immune response and produced high titers of high avidity polyclonal antibodies. Investigation of the neutralizing activity of the ovine antisera in vitro revealed that it neutralized EBOV. A pool of intact ovine immunoglobulin G, herein termed EBOTAb, was prepared from the antisera and used for an in vivo guinea pig study. When EBOTAb was delivered 6 hours after challenge, all animals survived without experiencing fever or other clinical manifestations. In a second series of guinea pig studies, the administration of EBOTAb dosing was delayed for 48 or 72 hours after challenge, resulting in 100% and 75% survival, respectively. These studies illustrate the usefulness of EBOTAb in protecting against EBOV-induced disease.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Immunoglobulin G / Membrane Glycoproteins / Glycoproteins / Hemorrhagic Fever, Ebola / Ebolavirus / Antibodies, Viral Type of study: Health_economic_evaluation Limits: Animals / Female / Humans Language: En Journal: J Infect Dis Year: 2016 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Immunoglobulin G / Membrane Glycoproteins / Glycoproteins / Hemorrhagic Fever, Ebola / Ebolavirus / Antibodies, Viral Type of study: Health_economic_evaluation Limits: Animals / Female / Humans Language: En Journal: J Infect Dis Year: 2016 Document type: Article