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Increased ERK and JNK activities correlate with disease activity in patients with systemic lupus erythematosus

激酶 MAPK/ERK通路 医学 外周血单个核细胞 丝裂原活化蛋白激酶 内科学 免疫学 化学 体外 生物化学
作者
Yair Molad,M Amit-Vasina,Olga Bloch,Yona Eli,Micha J. Rapoport
出处
期刊:Annals of the Rheumatic Diseases [BMJ]
卷期号:69 (01): 175-180 被引量:32
标识
DOI:10.1136/ard.2008.102780
摘要

Background: Aberrant signalling along the p21ras/MAP kinase pathway has been demonstrated in systemic lupus erythematosus (SLE). Objective: To determine whether expression and activity of the MAP kinases ERK and JNK reflect disease activity in patients with SLE. Methods: Blood samples of 42 outpatients with SLE were prospectively collected during four consecutive visits. The control group included 20 healthy subjects. Disease activity was assessed using the SLE Disease Activity Index (SLEDAI). Expression of total ERK and JNK kinases and their active forms (pERK and pJNK) was determined in whole protein lysates of peripheral blood mononuclear cells. Results: The mean levels of the active kinases pERK and pJNK were significantly increased in patients with active disease (SLEDAI 4–20) as compared with patients with inactive disease (SLEDAI 0–3), p = 0.04, as well as with healthy controls, p = 0.03 and p = 0.003 for pERK and pJNK, respectively. The percentage of activated forms of ERK and JNK of the total expression of these MAP kinases was also gradually increased, reaching 50% for pERK and >40% for pJNK in patients with SLE with moderate-to-severe disease (SLEDAI 7–20), p = 0.005, p = 0.005 and p = 0.02, p = 0.05 as compared with controls and inactive patients, respectively. A decrease of more than three SLEDAI points was associated with a significant reduction in the expression of both total and activated forms of ERK and JNK, p = 0.03, p = 0.01, respectively. Conclusions: The results show that ERK and JNK activity reflects disease activity in patients with SLE. These MAP kinases may serve as additional tools for the evaluation of disease activity and management of these patients.
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