First Affiliated Hospital of China Medical University, Nanjing North Street 155, Shenyang 110001, China.
Cytokine. 2011 Mar;53(3):289-91. doi: 10.1016/j.cyto.2010.12.003. Epub 2010 Dec 28.
We measured serum levels of Tumor necrosis factor (TNF)-like weak inducer of apoptosis (TWEAK), interleukin 15 (IL-15), monocyte chemoattractant protein 1 (MCP-1), and matrix metalloproteinase (MMP)-3 for patients with Psoriatic arthritis (PsA), and investigated whether TWEAK levels are associated with clinical disease activity and expression of proinflammatory cytokines.
Forty five patients with PsA and forty five patients with osteoarthritis (OA) were involved in this study between January 2008 and December 2009. At the time of blood sample collection, the disease activity of patients with PsA was assessed according to the 28-joint count Disease Activity Score (DAS28). Serum levels of TWEAK, IL-15, MCP-1, and MMP-3 were measured using commercial enzyme-linked immunosorbent assay (ELISA) kits according to the manufacturers' protocol.
In patients with PsA, serum TWEAK, IL-15, MCP-1 and MMP-3 levels were significantly elevated, and serum TWEAK levels showed a significant correlation with DAS28 (r=0.405, p=0.006) and serum MMP-3 levels (r=0.375, p=0.011).
Serum TWEAK levels positively correlate with disease activity of PsA and confirm that TWEAK plays a crucial role in the pathogenesis of PsA. TWEAK may be a new important target for therapy in PsA.
我们测量了肿瘤坏死因子样凋亡弱诱导物(TWEAK)、白细胞介素 15(IL-15)、单核细胞趋化蛋白 1(MCP-1)和基质金属蛋白酶(MMP-3)在银屑病关节炎(PsA)患者中的血清水平,并研究了 TWEAK 水平是否与临床疾病活动和促炎细胞因子的表达有关。
2008 年 1 月至 2009 年 12 月期间,我们共纳入了 45 例 PsA 患者和 45 例骨关节炎(OA)患者。在采集血样时,根据 28 关节疾病活动评分(DAS28)评估 PsA 患者的疾病活动度。采用商业酶联免疫吸附试验(ELISA)试剂盒,按照制造商的方案,测定 TWEAK、IL-15、MCP-1 和 MMP-3 的血清水平。
在 PsA 患者中,血清 TWEAK、IL-15、MCP-1 和 MMP-3 水平显著升高,血清 TWEAK 水平与 DAS28 呈显著正相关(r=0.405,p=0.006),与血清 MMP-3 水平呈显著正相关(r=0.375,p=0.011)。
血清 TWEAK 水平与 PsA 的疾病活动度呈正相关,证实 TWEAK 在 PsA 的发病机制中起关键作用。TWEAK 可能成为 PsA 治疗的新的重要靶点。