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Prevention and treatment of Clostridium perfringens epsilon toxin intoxication in mice with a neutralizing monoclonal antibody (c4D7) produced in Nicotiana benthamiana.
Garcia, J P; Beingesser, J; Bohorov, O; Bohorova, N; Goodman, C; Kim, D; Pauly, M; Velasco, J; Whaley, K; Zeitlin, L; Roy, C J; Uzal, F A.
Afiliación
  • Garcia JP; California Animal Health and Food Safety Laboratory System, San Bernardino Branch, School of Veterinary Medicine, University of California, Davis, San Bernardino, CA 92408, USA.
  • Beingesser J; California Animal Health and Food Safety Laboratory System, San Bernardino Branch, School of Veterinary Medicine, University of California, Davis, San Bernardino, CA 92408, USA.
  • Bohorov O; Mapp Biopharmaceutical, Inc., San Diego, CA, USA.
  • Bohorova N; Mapp Biopharmaceutical, Inc., San Diego, CA, USA.
  • Goodman C; Mapp Biopharmaceutical, Inc., San Diego, CA, USA.
  • Kim D; Mapp Biopharmaceutical, Inc., San Diego, CA, USA.
  • Pauly M; Mapp Biopharmaceutical, Inc., San Diego, CA, USA.
  • Velasco J; Mapp Biopharmaceutical, Inc., San Diego, CA, USA.
  • Whaley K; Mapp Biopharmaceutical, Inc., San Diego, CA, USA.
  • Zeitlin L; Mapp Biopharmaceutical, Inc., San Diego, CA, USA.
  • Roy CJ; Microbiology Division, Tulane National Primate Research Center, Covington, LA, USA.
  • Uzal FA; California Animal Health and Food Safety Laboratory System, San Bernardino Branch, School of Veterinary Medicine, University of California, Davis, San Bernardino, CA 92408, USA. Electronic address: fuzal@cahfs.ucdavis.edu.
Toxicon ; 88: 93-8, 2014 Sep.
Article en En | MEDLINE | ID: mdl-24950050
Epsilon toxin (ETX), produced by Clostridium perfringens types B and D, is among the most lethal toxins known. ETX is a potential bioterrorism threat that was listed as a Category B agent by the U.S. Centers for Disease Control until 2012 and it still remains a toxin of interest for several government agencies. We produced a monoclonal antibody (MAb) against ETX (ETX MAb c4D7) in Nicotiana benthamiana and characterized its preventive and therapeutic efficacy in mice. The ETX preparation used was highly lethal for mice (LD50 = 1.6 µg/kg) and resulted in a mean time from inoculation to death of 18 and 180 min when administered intravenously or intraperitoneally, respectively. High lethal challenge resulted in dramatic increases of a variety of pro-inflammatory cytokines in serum, while lower, but still lethal doses, did not elicit such responses. ETX MAb c4D7 was highly effective prophylactically (ED50 = 0.3 mg/kg; ED100 = 0.8 mg/kg) and also provided protection when delivered 15-30 min post-ETX intoxication. These data suggest that ETX MAb c4D7 may have use as a pre- and post-exposure treatment for ETX intoxication.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Nicotiana / Toxinas Bacterianas / Anticuerpos Neutralizantes / Anticuerpos Monoclonales Límite: Animals Idioma: En Revista: Toxicon Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Nicotiana / Toxinas Bacterianas / Anticuerpos Neutralizantes / Anticuerpos Monoclonales Límite: Animals Idioma: En Revista: Toxicon Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido