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Targeted Secretion Inhibitors—Innovative Protein Therapeutics

Botulinum neurotoxins are highly effective therapeutic products. Their therapeutic success results from highly specific and potent inhibition of neurotransmitter release with a duration of action measured in months. These same properties, however, make the botulinum neurotoxins the most potent acute...

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Detalles Bibliográficos
Autores principales: Foster, Keith, Chaddock, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3153183/
https://www.ncbi.nlm.nih.gov/pubmed/22069575
http://dx.doi.org/10.3390/toxins2122795
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author Foster, Keith
Chaddock, John
author_facet Foster, Keith
Chaddock, John
author_sort Foster, Keith
collection PubMed
description Botulinum neurotoxins are highly effective therapeutic products. Their therapeutic success results from highly specific and potent inhibition of neurotransmitter release with a duration of action measured in months. These same properties, however, make the botulinum neurotoxins the most potent acute lethal toxins known. Their toxicity and restricted target cell activity severely limits their clinical utility. Understanding the structure-function relationship of the neurotoxins has enabled the development of recombinant proteins selectively incorporating specific aspects of their pharmacology. The resulting proteins are not neurotoxins, but a new class of biopharmaceuticals, Targeted Secretion Inhibitors (TSI), suitable for the treatment of a wide range of diseases where secretion plays a major role. TSI proteins inhibit secretion for a prolonged period following a single application, making them particularly suited to the treatment of chronic diseases. A TSI for the treatment of chronic pain is in clinical development.
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spelling pubmed-31531832011-11-08 Targeted Secretion Inhibitors—Innovative Protein Therapeutics Foster, Keith Chaddock, John Toxins (Basel) Review Botulinum neurotoxins are highly effective therapeutic products. Their therapeutic success results from highly specific and potent inhibition of neurotransmitter release with a duration of action measured in months. These same properties, however, make the botulinum neurotoxins the most potent acute lethal toxins known. Their toxicity and restricted target cell activity severely limits their clinical utility. Understanding the structure-function relationship of the neurotoxins has enabled the development of recombinant proteins selectively incorporating specific aspects of their pharmacology. The resulting proteins are not neurotoxins, but a new class of biopharmaceuticals, Targeted Secretion Inhibitors (TSI), suitable for the treatment of a wide range of diseases where secretion plays a major role. TSI proteins inhibit secretion for a prolonged period following a single application, making them particularly suited to the treatment of chronic diseases. A TSI for the treatment of chronic pain is in clinical development. MDPI 2010-12-03 /pmc/articles/PMC3153183/ /pubmed/22069575 http://dx.doi.org/10.3390/toxins2122795 Text en © 2010 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Foster, Keith
Chaddock, John
Targeted Secretion Inhibitors—Innovative Protein Therapeutics
title Targeted Secretion Inhibitors—Innovative Protein Therapeutics
title_full Targeted Secretion Inhibitors—Innovative Protein Therapeutics
title_fullStr Targeted Secretion Inhibitors—Innovative Protein Therapeutics
title_full_unstemmed Targeted Secretion Inhibitors—Innovative Protein Therapeutics
title_short Targeted Secretion Inhibitors—Innovative Protein Therapeutics
title_sort targeted secretion inhibitors—innovative protein therapeutics
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3153183/
https://www.ncbi.nlm.nih.gov/pubmed/22069575
http://dx.doi.org/10.3390/toxins2122795
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