Please use this identifier to cite or link to this item: https://doi.org/10.1186/ar2365
Title: Cartilage preservation by inhibition of Janus kinase 3 in two rodent models of rheumatoid arthritis
Authors: Milici, A.J
Kudlacz, E.M
Audoly, L 
Zwillich, S
Changelian, P
Keywords: 4 [n [1 (2 cyano 1 oxoethyl) 4 methyl 3 piperidinyl] n methylamino]pyrrolo[2,3 d]pyrimidine
interleukin 6
Janus kinase 3
tumor necrosis factor antibody
collagen
CP 690,550
CP-690,550
enzyme inhibitor
immunological adjuvant
interleukin 6
Janus kinase 3
pyrimidine derivative
pyrrole derivative
adjuvant arthritis
animal cell
animal experiment
animal model
animal tissue
article
chondroprotection
controlled study
DBA 1 mouse
dose response
drug blood level
drug dose comparison
drug efficacy
drug megadose
drug targeting
enzyme inhibition
Lewis rat
low drug dose
male
mouse
nonhuman
paw edema
protein blood level
rat
rheumatoid arthritis
scoring system
animal
arthritis
articular cartilage
blood
DBA mouse
drug antagonism
enzymology
immunology
pathology
rheumatoid arthritis
Adjuvants, Immunologic
Animals
Arthritis, Experimental
Arthritis, Rheumatoid
Cartilage, Articular
Collagen
Dose-Response Relationship, Drug
Enzyme Inhibitors
Interleukin-6
Janus Kinase 3
Male
Mice
Mice, Inbred DBA
Pyrimidines
Pyrroles
Rats
Rats, Inbred Lew
Issue Date: 2008
Citation: Milici, A.J, Kudlacz, E.M, Audoly, L, Zwillich, S, Changelian, P (2008). Cartilage preservation by inhibition of Janus kinase 3 in two rodent models of rheumatoid arthritis. Arthritis Research and Therapy 10 (1) : R14. ScholarBank@NUS Repository. https://doi.org/10.1186/ar2365
Rights: Attribution 4.0 International
Abstract: 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 ED50 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. © 2008 Milici et al.; licensee BioMed Central Ltd.
Source Title: Arthritis Research and Therapy
URI: https://scholarbank.nus.edu.sg/handle/10635/177981
ISSN: 14786354
DOI: 10.1186/ar2365
Rights: Attribution 4.0 International
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