MMP-2, MMP-9, TIMP-1 and TIMP-2 levels in patients with rheumatoid arthritis and psoriatic arthritis

被引:1
|
作者
Giannelli, G
Erriquez, R
Iannone, F
Marinosci, F
Lapadula, G
Antonaci, S
机构
[1] Cesare Frugoni Policlin, Dipartimento Clin Med Immunol & Malattie Infett C, I-70124 Bari, Italy
[2] Univ Bari, Sch Med, Dept Internal Med & Publ Med, Rheumatol Unit, Bari, Italy
[3] Univ Bari, Sch Med, Dept Internal Med Immunol & Infect Dis, Sect Internal Med, Bari, Italy
关键词
matrix metalloproteases; gelatinases; rheumatoid arthritis; psoriatic arthritis;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. Rheumatoid arthritis (RA) and psoriatic arthritis (PA) are both chronic rheumatic inflammatory diseases characterized by disruption of the extra-cellular matrix (ECM) protein of the cartilage, likely induced by proteolytic enzymes such as matrix metalloproteases (MMPs). The goal of this study was to quantify the expression of MMPs such as MMP-2 and MMP-9, and their physiological tissue inhibitors TIMP-2 and TIMP-1, respectively, in serum and synovial fluid. Methods. Serum and synovial fluid from 24 RA patients and 17 PA patients were studied to determine the levels of MMP-2 and MMP-9 proteolytic activity using a modified gelatin zymography procedure. TIMP-1 and TIMP-2 were measured by a commercially available ELISA kit. Results. Our results show that MMP-2 was detected in the latent form only, while MMP-9 was present in latent and active form. Both gelatinases were more concentrated in synovial fluid than in serum, and TIMP-1 and TIMP-2 concentrations were also more elevated in synovial fluid than in serum. Conclusions. To investigate the remodelling of cartilage ECM proteins, the evaluation of synovial fluid concentrations of MMP-2, MMP-9, TIMP-1 and TIMP-2 is more reliable than that determined in serum. In view of these data, MMPs inhibitors might represent a possible target for new therapies delivered directly in the joint space.
引用
收藏
页码:335 / 338
页数:4
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