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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 |
Appears in Collections: | Elements Staff Publications |
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