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Reversion of Ebolavirus Disease from a Single Intramuscular Injection of a Pan-Ebolavirus Immunotherapeutic.
Kuang, Erin; Cross, Robert W; McCavitt-Malvido, Maria; Abelson, Dafna M; Borisevich, Viktoriya; Stuart, Lauren; Agans, Krystle N; Mlakar, Neil; Marimuthu, Arumugapradeep; Deer, Daniel J; Shestowsky, William S; Kim, Do; Geisbert, Joan B; Zeitlin, Larry; Moyer, Crystal L; Roy, Chad J; Geisbert, Thomas W; Bornholdt, Zachary A.
Afiliação
  • Kuang E; Mapp Biopharmaceutical, Inc., San Diego, CA 92121, USA.
  • Cross RW; Galveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555, USA.
  • McCavitt-Malvido M; Mapp Biopharmaceutical, Inc., San Diego, CA 92121, USA.
  • Abelson DM; Mapp Biopharmaceutical, Inc., San Diego, CA 92121, USA.
  • Borisevich V; Galveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555, USA.
  • Stuart L; Mapp Biopharmaceutical, Inc., San Diego, CA 92121, USA.
  • Agans KN; Galveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555, USA.
  • Mlakar N; Mapp Biopharmaceutical, Inc., San Diego, CA 92121, USA.
  • Marimuthu A; Mapp Biopharmaceutical, Inc., San Diego, CA 92121, USA.
  • Deer DJ; Galveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555, USA.
  • Shestowsky WS; Mapp Biopharmaceutical, Inc., San Diego, CA 92121, USA.
  • Kim D; Mapp Biopharmaceutical, Inc., San Diego, CA 92121, USA.
  • Geisbert JB; Galveston National Laboratory, University of Texas Medical Branch, Galveston, TX 77555, USA.
  • Zeitlin L; Mapp Biopharmaceutical, Inc., San Diego, CA 92121, USA.
  • Moyer CL; Mapp Biopharmaceutical, Inc., San Diego, CA 92121, USA.
  • Roy CJ; Eitr Biologics, Inc., San Diego, CA 92121, USA.
  • Geisbert TW; Department of Microbiology and Immunology, Tulane School of Medicine, New Orleans, LA 70112, USA.
  • Bornholdt ZA; Division of Microbiology, Tulane National Primate Research Center, Covington, LA 70447, USA.
Pathogens ; 11(6)2022 Jun 07.
Article em En | MEDLINE | ID: mdl-35745509
ABSTRACT
Intravenous (IV) administration of antiviral monoclonal antibodies (mAbs) can be challenging, particularly during an ongoing epidemic, due to the considerable resources required for performing infusions. An ebolavirus therapeutic administered via intramuscular (IM) injection would reduce the burdens associated with IV infusion and allow rapid treatment of exposed individuals during an outbreak. Here, we demonstrate how MBP134, a cocktail of two pan-ebolavirus mAbs, reverses the course of Sudan ebolavirus disease (Gulu variant) with a single IV or IM dose in non-human primates (NHPs) as late as five days post-exposure. We also investigate the utility of adding half-life extension mutations to the MBP134 mAbs, ultimately creating a half-life extended cocktail designated MBP431. When delivered as a post-exposure prophylactic or therapeutic, a single IM dose of MBP431 offered complete or significant protection in NHPs challenged with Zaire ebolavirus. In conjunction with previous studies, these results support the use of MBP431 as a rapidly deployable IM medical countermeasure against every known species of ebolavirus.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article