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Production, Characterisation and Testing of an Ovine Antitoxin against Ricin; Efficacy, Potency and Mechanisms of Action
Ricin is a type II ribosome-inactivating toxin that catalytically inactivates ribosomes ultimately leading to cell death. The toxicity of ricin along with the prevalence of castor beans (its natural source) has led to its increased notoriety and incidences of nefarious use. Despite these concerns, t...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666376/ https://www.ncbi.nlm.nih.gov/pubmed/29057798 http://dx.doi.org/10.3390/toxins9100329 |
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author | Whitfield, Sarah J. C. Griffiths, Gareth D. Jenner, Dominic C. Gwyther, Robert J. Stahl, Fiona M. Cork, Lucy J. Holley, Jane L. Green, A. Christopher Clark, Graeme C. |
author_facet | Whitfield, Sarah J. C. Griffiths, Gareth D. Jenner, Dominic C. Gwyther, Robert J. Stahl, Fiona M. Cork, Lucy J. Holley, Jane L. Green, A. Christopher Clark, Graeme C. |
author_sort | Whitfield, Sarah J. C. |
collection | PubMed |
description | Ricin is a type II ribosome-inactivating toxin that catalytically inactivates ribosomes ultimately leading to cell death. The toxicity of ricin along with the prevalence of castor beans (its natural source) has led to its increased notoriety and incidences of nefarious use. Despite these concerns, there are no licensed therapies available for treating ricin intoxication. Here, we describe the development of a F(ab’)(2) polyclonal ovine antitoxin against ricin and demonstrate the efficacy of a single, post-exposure, administration in an in vivo murine model of intoxication against aerosolised ricin. We found that a single dose of antitoxin afforded a wide window of opportunity for effective treatment with 100% protection observed in mice challenged with aerosolised ricin when given 24 h after exposure to the toxin and 75% protection when given at 30 h. Treated mice had reduced weight loss and clinical signs of intoxication compared to the untreated control group. Finally, using imaging flow cytometry, it was found that both cellular uptake and intracellular trafficking of ricin toxin to the Golgi apparatus was reduced in the presence of the antitoxin suggesting both actions can contribute to the therapeutic mechanism of a polyclonal antitoxin. Collectively, the research highlights the significant potential of the ovine F(ab’)(2) antitoxin as a treatment for ricin intoxication. |
format | Online Article Text |
id | pubmed-5666376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-56663762017-11-09 Production, Characterisation and Testing of an Ovine Antitoxin against Ricin; Efficacy, Potency and Mechanisms of Action Whitfield, Sarah J. C. Griffiths, Gareth D. Jenner, Dominic C. Gwyther, Robert J. Stahl, Fiona M. Cork, Lucy J. Holley, Jane L. Green, A. Christopher Clark, Graeme C. Toxins (Basel) Article Ricin is a type II ribosome-inactivating toxin that catalytically inactivates ribosomes ultimately leading to cell death. The toxicity of ricin along with the prevalence of castor beans (its natural source) has led to its increased notoriety and incidences of nefarious use. Despite these concerns, there are no licensed therapies available for treating ricin intoxication. Here, we describe the development of a F(ab’)(2) polyclonal ovine antitoxin against ricin and demonstrate the efficacy of a single, post-exposure, administration in an in vivo murine model of intoxication against aerosolised ricin. We found that a single dose of antitoxin afforded a wide window of opportunity for effective treatment with 100% protection observed in mice challenged with aerosolised ricin when given 24 h after exposure to the toxin and 75% protection when given at 30 h. Treated mice had reduced weight loss and clinical signs of intoxication compared to the untreated control group. Finally, using imaging flow cytometry, it was found that both cellular uptake and intracellular trafficking of ricin toxin to the Golgi apparatus was reduced in the presence of the antitoxin suggesting both actions can contribute to the therapeutic mechanism of a polyclonal antitoxin. Collectively, the research highlights the significant potential of the ovine F(ab’)(2) antitoxin as a treatment for ricin intoxication. MDPI 2017-10-18 /pmc/articles/PMC5666376/ /pubmed/29057798 http://dx.doi.org/10.3390/toxins9100329 Text en © Crown copyright (2017), Dstl. This material is licensed under the terms of the Open Government Licence except where otherwise stated. To view this licence, visit: http://www.nationalarchives.gov.uk/doc/open-government-licence/version/3 or write to the Information Policy Team, The National Archives, Kew, London TW9 4DU, or email: psi@nationalarchives.gsi.gov.uk. |
spellingShingle | Article Whitfield, Sarah J. C. Griffiths, Gareth D. Jenner, Dominic C. Gwyther, Robert J. Stahl, Fiona M. Cork, Lucy J. Holley, Jane L. Green, A. Christopher Clark, Graeme C. Production, Characterisation and Testing of an Ovine Antitoxin against Ricin; Efficacy, Potency and Mechanisms of Action |
title | Production, Characterisation and Testing of an Ovine Antitoxin against Ricin; Efficacy, Potency and Mechanisms of Action |
title_full | Production, Characterisation and Testing of an Ovine Antitoxin against Ricin; Efficacy, Potency and Mechanisms of Action |
title_fullStr | Production, Characterisation and Testing of an Ovine Antitoxin against Ricin; Efficacy, Potency and Mechanisms of Action |
title_full_unstemmed | Production, Characterisation and Testing of an Ovine Antitoxin against Ricin; Efficacy, Potency and Mechanisms of Action |
title_short | Production, Characterisation and Testing of an Ovine Antitoxin against Ricin; Efficacy, Potency and Mechanisms of Action |
title_sort | production, characterisation and testing of an ovine antitoxin against ricin; efficacy, potency and mechanisms of action |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666376/ https://www.ncbi.nlm.nih.gov/pubmed/29057798 http://dx.doi.org/10.3390/toxins9100329 |
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