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Efficacy of Bioactive Cyclic Peptides in Rheumatoid Arthritis: Translation from In Vitro to In Vivo Models

Using a novel drug discovery technology reported in previous issues of this journal cyclic peptides have been created which are able to down-regulate secretion of inflammatory cytokines, in vitro, by stimulated cells of the macrophage cell line J774. The cytokines in question, TNF-alpha and IL-6, ar...

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Autores principales: New, Roger, Bogus, Michal, Bansal, Gurpal S., Dryjska, Malgorzata, Zajkowska, Katarzyna, Burnet, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151468/
https://www.ncbi.nlm.nih.gov/pubmed/28946707
http://dx.doi.org/10.3390/molecules22101613
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author New, Roger
Bogus, Michal
Bansal, Gurpal S.
Dryjska, Malgorzata
Zajkowska, Katarzyna
Burnet, Michael
author_facet New, Roger
Bogus, Michal
Bansal, Gurpal S.
Dryjska, Malgorzata
Zajkowska, Katarzyna
Burnet, Michael
author_sort New, Roger
collection PubMed
description Using a novel drug discovery technology reported in previous issues of this journal cyclic peptides have been created which are able to down-regulate secretion of inflammatory cytokines, in vitro, by stimulated cells of the macrophage cell line J774. The cytokines in question, TNF-alpha and IL-6, are strongly implicated in etiology of diseases such as rheumatoid arthritis. Studies are reported here using the CAIA animal model for rheumatoid arthritis, which show that the peptides identified are indeed able to impact on inflammation of joints, induced in vivo. The results suggest that these peptides are effective at a dose which could be viable in man, and at which no adverse side effects are evident in the short term.
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spelling pubmed-61514682018-11-13 Efficacy of Bioactive Cyclic Peptides in Rheumatoid Arthritis: Translation from In Vitro to In Vivo Models New, Roger Bogus, Michal Bansal, Gurpal S. Dryjska, Malgorzata Zajkowska, Katarzyna Burnet, Michael Molecules Article Using a novel drug discovery technology reported in previous issues of this journal cyclic peptides have been created which are able to down-regulate secretion of inflammatory cytokines, in vitro, by stimulated cells of the macrophage cell line J774. The cytokines in question, TNF-alpha and IL-6, are strongly implicated in etiology of diseases such as rheumatoid arthritis. Studies are reported here using the CAIA animal model for rheumatoid arthritis, which show that the peptides identified are indeed able to impact on inflammation of joints, induced in vivo. The results suggest that these peptides are effective at a dose which could be viable in man, and at which no adverse side effects are evident in the short term. MDPI 2017-09-25 /pmc/articles/PMC6151468/ /pubmed/28946707 http://dx.doi.org/10.3390/molecules22101613 Text en © 2017 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
New, Roger
Bogus, Michal
Bansal, Gurpal S.
Dryjska, Malgorzata
Zajkowska, Katarzyna
Burnet, Michael
Efficacy of Bioactive Cyclic Peptides in Rheumatoid Arthritis: Translation from In Vitro to In Vivo Models
title Efficacy of Bioactive Cyclic Peptides in Rheumatoid Arthritis: Translation from In Vitro to In Vivo Models
title_full Efficacy of Bioactive Cyclic Peptides in Rheumatoid Arthritis: Translation from In Vitro to In Vivo Models
title_fullStr Efficacy of Bioactive Cyclic Peptides in Rheumatoid Arthritis: Translation from In Vitro to In Vivo Models
title_full_unstemmed Efficacy of Bioactive Cyclic Peptides in Rheumatoid Arthritis: Translation from In Vitro to In Vivo Models
title_short Efficacy of Bioactive Cyclic Peptides in Rheumatoid Arthritis: Translation from In Vitro to In Vivo Models
title_sort efficacy of bioactive cyclic peptides in rheumatoid arthritis: translation from in vitro to in vivo models
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151468/
https://www.ncbi.nlm.nih.gov/pubmed/28946707
http://dx.doi.org/10.3390/molecules22101613
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