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A Monoclonal Antibody Combination against both Serotypes A and B Botulinum Toxin Prevents Inhalational Botulism in a Guinea Pig Model

Botulinum neurotoxins (BoNT) are extremely potent and can induce respiratory failure, requiring long-term intensive care to prevent death. Recombinant monoclonal antibodies (mAbs) hold considerable promise as BoNT therapeutics and prophylactics. In contrast, equine antitoxin cannot be used prophylac...

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Autores principales: Snow, Doris M., Cobb, Ronald R., Martinez, Juan, Finger-Baker, Isaac, Collins, Laura, Terpening, Sara, Syar, Emily S., Niemuth, Nancy, Kobs, Dean, Barnewall, Roy, Farr-Jones, Shauna, Marks, James D., Tomic, Milan T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824882/
https://www.ncbi.nlm.nih.gov/pubmed/33466411
http://dx.doi.org/10.3390/toxins13010031
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author Snow, Doris M.
Cobb, Ronald R.
Martinez, Juan
Finger-Baker, Isaac
Collins, Laura
Terpening, Sara
Syar, Emily S.
Niemuth, Nancy
Kobs, Dean
Barnewall, Roy
Farr-Jones, Shauna
Marks, James D.
Tomic, Milan T.
author_facet Snow, Doris M.
Cobb, Ronald R.
Martinez, Juan
Finger-Baker, Isaac
Collins, Laura
Terpening, Sara
Syar, Emily S.
Niemuth, Nancy
Kobs, Dean
Barnewall, Roy
Farr-Jones, Shauna
Marks, James D.
Tomic, Milan T.
author_sort Snow, Doris M.
collection PubMed
description Botulinum neurotoxins (BoNT) are extremely potent and can induce respiratory failure, requiring long-term intensive care to prevent death. Recombinant monoclonal antibodies (mAbs) hold considerable promise as BoNT therapeutics and prophylactics. In contrast, equine antitoxin cannot be used prophylactically and has a short half-life. Two three-mAb combinations are in development that specifically neutralize BoNT serotype A (BoNT/A) and B (BoNT/B). The three-mAb combinations addressing a single serotype provided pre-exposure prophylaxis in the guinea pig inhalation model. A lyophilized co-formulation of six mAbs, designated G03-52-01, that addresses both A and B serotypes is in development. Here, we investigated the efficacy of G03-52-01 to protect guinea pigs against an aerosol exposure challenge of BoNT/A1 or BoNT/B1. Previously, it was found that each antibody demonstrated a dose-dependent exposure and reached maximum circulating concentrations within 48 h after intramuscular (IM) or intravenous (IV) injection. Here we show that G03-52-01, in a single IM injection of G03-52-01 administered 48 h pre-exposure, protected guinea pigs against an aerosol challenge of up to 238 LD(50)s of BoNT/A1 and 191 LD(50)s of BoNT/B1. These data suggest that a single IM administration of G03-52-01 provides pre-exposure prophylaxis against botulism from an aerosol exposure of BoNT/A1 or BoNT/B1.
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spelling pubmed-78248822021-01-24 A Monoclonal Antibody Combination against both Serotypes A and B Botulinum Toxin Prevents Inhalational Botulism in a Guinea Pig Model Snow, Doris M. Cobb, Ronald R. Martinez, Juan Finger-Baker, Isaac Collins, Laura Terpening, Sara Syar, Emily S. Niemuth, Nancy Kobs, Dean Barnewall, Roy Farr-Jones, Shauna Marks, James D. Tomic, Milan T. Toxins (Basel) Article Botulinum neurotoxins (BoNT) are extremely potent and can induce respiratory failure, requiring long-term intensive care to prevent death. Recombinant monoclonal antibodies (mAbs) hold considerable promise as BoNT therapeutics and prophylactics. In contrast, equine antitoxin cannot be used prophylactically and has a short half-life. Two three-mAb combinations are in development that specifically neutralize BoNT serotype A (BoNT/A) and B (BoNT/B). The three-mAb combinations addressing a single serotype provided pre-exposure prophylaxis in the guinea pig inhalation model. A lyophilized co-formulation of six mAbs, designated G03-52-01, that addresses both A and B serotypes is in development. Here, we investigated the efficacy of G03-52-01 to protect guinea pigs against an aerosol exposure challenge of BoNT/A1 or BoNT/B1. Previously, it was found that each antibody demonstrated a dose-dependent exposure and reached maximum circulating concentrations within 48 h after intramuscular (IM) or intravenous (IV) injection. Here we show that G03-52-01, in a single IM injection of G03-52-01 administered 48 h pre-exposure, protected guinea pigs against an aerosol challenge of up to 238 LD(50)s of BoNT/A1 and 191 LD(50)s of BoNT/B1. These data suggest that a single IM administration of G03-52-01 provides pre-exposure prophylaxis against botulism from an aerosol exposure of BoNT/A1 or BoNT/B1. MDPI 2021-01-05 /pmc/articles/PMC7824882/ /pubmed/33466411 http://dx.doi.org/10.3390/toxins13010031 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Snow, Doris M.
Cobb, Ronald R.
Martinez, Juan
Finger-Baker, Isaac
Collins, Laura
Terpening, Sara
Syar, Emily S.
Niemuth, Nancy
Kobs, Dean
Barnewall, Roy
Farr-Jones, Shauna
Marks, James D.
Tomic, Milan T.
A Monoclonal Antibody Combination against both Serotypes A and B Botulinum Toxin Prevents Inhalational Botulism in a Guinea Pig Model
title A Monoclonal Antibody Combination against both Serotypes A and B Botulinum Toxin Prevents Inhalational Botulism in a Guinea Pig Model
title_full A Monoclonal Antibody Combination against both Serotypes A and B Botulinum Toxin Prevents Inhalational Botulism in a Guinea Pig Model
title_fullStr A Monoclonal Antibody Combination against both Serotypes A and B Botulinum Toxin Prevents Inhalational Botulism in a Guinea Pig Model
title_full_unstemmed A Monoclonal Antibody Combination against both Serotypes A and B Botulinum Toxin Prevents Inhalational Botulism in a Guinea Pig Model
title_short A Monoclonal Antibody Combination against both Serotypes A and B Botulinum Toxin Prevents Inhalational Botulism in a Guinea Pig Model
title_sort monoclonal antibody combination against both serotypes a and b botulinum toxin prevents inhalational botulism in a guinea pig model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7824882/
https://www.ncbi.nlm.nih.gov/pubmed/33466411
http://dx.doi.org/10.3390/toxins13010031
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