Thioredoxin as a biomarker for oxidative stress in patients with rheumatoid arthritis

被引:135
作者
Jikimoto, T
Nishikubo, Y
Koshiba, M
Kanagawa, S
Morinobu, S
Morinobu, A
Saura, R
Mizuno, K
Kondo, S
Toyokuni, S
Nakamura, H
Yodoi, J
Kumagai, S
机构
[1] Kobe Univ, Grad Sch Med, Dept Clin Pathol & Immunol, Chuou Ku, Kobe, Hyogo 6500017, Japan
[2] Kobe Univ, Grad Sch Med, Dept Orthoped, Chuou Ku, Kobe, Hyogo 6500017, Japan
[3] Kyoto Univ, Grad Sch Med, Dept Pathol & Biol Dis, Sakyo Ku, Kyoto 6068501, Japan
[4] Kyoto Univ, Inst Viral Res, Dept Biol Responses, Sakyo Ku, Kyoto 6068507, Japan
基金
日本学术振兴会;
关键词
thioredoxin (TRX); rheumatoid arthritis; oxidative stress; 8-hydroxy-2 '-deoxyguanosine (8-OHdG); adult T-cell leukemia-derived factor (ADF);
D O I
10.1016/S0161-5890(01)00113-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There is no doubt that oxidative stress occurs in patients with rheumatoid arthritis (RA) and play an important role in both inflammation and destruction of RA joints. Thioredoxin (TRX) is a ubiquitous redox-active protein and is known to be induced in several cells against oxidative stress and to be secreted extracellularly. To clarify whether plasma thioredoxin levels could be a marker for oxidative stress in patients with RA, we measured plasma TRX levels in patients with RA using a sensitive sandwich enzyme-linked immunosorbent assay (ELISA) and investigated its relationship to TRX concentrations in the inflammatory joints. We have found that the plasma TRX levels of RA patients were significantly higher than those of normal subjects (86.8 +/- 54.1 ng/ml versus 38.61 +/- 18.5 ng/ml, P < 0.0001). The plasma levels were correlated with the disease activity of RA and also with serum C-reactive protein (CRP) values (P < 0.01). The concentration of TRX in synovial fluid (SF) from RA was 353.3 +/- 220.1 n/ml (mean S.D.) which was significantly higher than that in SF from osteoarthritis patients (70.6 +/- 31.0 ng/ml, P < 0.0001). The SF TRX concentration was significantly correlated with the number of leukocytes infiltrating in SF and with the serum CRP levels. The serum TRX levels were significantly positively correlated with the SFTRX concentrations in RA patients (P < 0.05). By the histological examination for synovial tissue of RA patients, TRX was shown to be present on the surface of synovial lining layer as well as in the leukocytes. Moreover, urinary excretion of 8-hydroxy-2'-deoxyguanosine (8-OHdG), a biomarker of oxidative DNA damage by endogenously generated oxygen radicals, was significantly higher in RA patients than in healthy subjects (11.55 +/- 4.71 versus 7.76 +/- 2.26 ng/mg creatinine, P < 0.0001). Plasma TRX levels were significantly correlated with urinary excretion of 8-OHdG (P < 0.005). We concluded that plasma TRX level is a new biomarker for the disease activity of RA and may reflect higher levels of oxidative stress in RA patients. 0 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:765 / 772
页数:8
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