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Cartilage preservation by inhibition of Janus kinase 3 in two rodent models of rheumatoid arthritis
INTRODUCTION: CP-690550 is a small molecule inhibitor of Janus kinase 3 (JAK3), a critical enzyme in the signaling pathway of multiple cytokines (interleukin (IL)-2, -7, -15 and -21) that are important in various T cell functions including development, activation and homeostasis. The purpose of this...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374467/ https://www.ncbi.nlm.nih.gov/pubmed/18234077 http://dx.doi.org/10.1186/ar2365 |
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author | Milici, Anthony J Kudlacz, Elizabeth M Audoly, Laurent Zwillich, Samuel Changelian, Paul |
author_facet | Milici, Anthony J Kudlacz, Elizabeth M Audoly, Laurent Zwillich, Samuel Changelian, Paul |
author_sort | Milici, Anthony J |
collection | PubMed |
description | INTRODUCTION: CP-690550 is a small molecule inhibitor of Janus kinase 3 (JAK3), a critical enzyme in the signaling pathway of multiple cytokines (interleukin (IL)-2, -7, -15 and -21) that are important in various T cell functions including development, activation and homeostasis. The purpose of this study was to evaluate CP-690550 in murine collagen-induced (CIA) and rat adjuvant-induced (AA) models of rheumatoid arthritis (RA). METHODS: CIA and AA were induced using standard protocols and animals received the JAK3 inhibitor via osmotic mini-pump infusion at doses ranging from 1.5–15 mg/kg/day following disease induction. Arthritis was assessed by clinical scores in the CIA models and paw swelling monitored using a plethysmometer in the AA model until study conclusion, at which time animals were killed and evaluated histologically. RESULTS: CP-690550 dose-dependently decreased endpoints of disease in both RA models with greater than 90% reduction observed at the highest administered dose. An approximate ED(50 )of approximately 1.5 mg/kg/day was determined for the compound based upon disease endpoints in both RA models examined and corresponds to CP-690550 serum levels of 5.8 ng/ml in mice (day 28) and 24 ng/ml in rats (day 24). The compound also reduced inflammatory cell influx and joint damage as measured histologically. Animals receiving a CP-690550 dose of 15 mg/k/d showed no histological evidence of disease. CONCLUSION: The efficacy observed with CP-690550 in CIA and AA suggests JAK3 inhibition may represent a novel therapeutic target for the treatment of RA. |
format | Text |
id | pubmed-2374467 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-23744672008-05-09 Cartilage preservation by inhibition of Janus kinase 3 in two rodent models of rheumatoid arthritis Milici, Anthony J Kudlacz, Elizabeth M Audoly, Laurent Zwillich, Samuel Changelian, Paul Arthritis Res Ther Research Article INTRODUCTION: CP-690550 is a small molecule inhibitor of Janus kinase 3 (JAK3), a critical enzyme in the signaling pathway of multiple cytokines (interleukin (IL)-2, -7, -15 and -21) that are important in various T cell functions including development, activation and homeostasis. The purpose of this study was to evaluate CP-690550 in murine collagen-induced (CIA) and rat adjuvant-induced (AA) models of rheumatoid arthritis (RA). METHODS: CIA and AA were induced using standard protocols and animals received the JAK3 inhibitor via osmotic mini-pump infusion at doses ranging from 1.5–15 mg/kg/day following disease induction. Arthritis was assessed by clinical scores in the CIA models and paw swelling monitored using a plethysmometer in the AA model until study conclusion, at which time animals were killed and evaluated histologically. RESULTS: CP-690550 dose-dependently decreased endpoints of disease in both RA models with greater than 90% reduction observed at the highest administered dose. An approximate ED(50 )of approximately 1.5 mg/kg/day was determined for the compound based upon disease endpoints in both RA models examined and corresponds to CP-690550 serum levels of 5.8 ng/ml in mice (day 28) and 24 ng/ml in rats (day 24). The compound also reduced inflammatory cell influx and joint damage as measured histologically. Animals receiving a CP-690550 dose of 15 mg/k/d showed no histological evidence of disease. CONCLUSION: The efficacy observed with CP-690550 in CIA and AA suggests JAK3 inhibition may represent a novel therapeutic target for the treatment of RA. BioMed Central 2008 2008-01-30 /pmc/articles/PMC2374467/ /pubmed/18234077 http://dx.doi.org/10.1186/ar2365 Text en Copyright © 2008 Milici et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Milici, Anthony J Kudlacz, Elizabeth M Audoly, Laurent Zwillich, Samuel Changelian, Paul Cartilage preservation by inhibition of Janus kinase 3 in two rodent models of rheumatoid arthritis |
title | Cartilage preservation by inhibition of Janus kinase 3 in two rodent models of rheumatoid arthritis |
title_full | Cartilage preservation by inhibition of Janus kinase 3 in two rodent models of rheumatoid arthritis |
title_fullStr | Cartilage preservation by inhibition of Janus kinase 3 in two rodent models of rheumatoid arthritis |
title_full_unstemmed | Cartilage preservation by inhibition of Janus kinase 3 in two rodent models of rheumatoid arthritis |
title_short | Cartilage preservation by inhibition of Janus kinase 3 in two rodent models of rheumatoid arthritis |
title_sort | cartilage preservation by inhibition of janus kinase 3 in two rodent models of rheumatoid arthritis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374467/ https://www.ncbi.nlm.nih.gov/pubmed/18234077 http://dx.doi.org/10.1186/ar2365 |
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