Agirbasli M, Inanc N, Baykan O A, Direskeneli H
Department of Cardiology, Marmara University School of Medicine, Istanbul, Turkey.
Clin Exp Rheumatol. 2006 Sep-Oct;24(5):580-3.
Recent studies support an inflammatory basis for atherosclerosis. Patients with chronic inflammatory rheumatical disorders are at increased risk for cardiovascular events, and this can be partially attributed to the inhibition of fibrinolytic system. TNF a inhibitors such as infliximab are shown to retard the progression of inflammatory arthritides. In this study, we investigated the effects of infliximab on plasma fibrinolytic parameters.
Thirteen patients (7 female, 6 male; mean age: 44 +/- 11 years) with a clinical indication for infliximab (rheumatoid arthritis (RA) (n = 8), ankylosing spondylitis (AS) (n = 5)) were selected. Plasma plasminogen activator inhibitor (PAI-1), tissue plasminogen activator (t-PA) antigens (Ag) and high sensitive C-reactive protein (hs-CRP) levels were measured during low salt intake at baseline. All patients received infliximab (Remicaide, i.v. infusion, 3 mg/kg). Plasma PAI-1 Ag, t-PA Ag and hs-CRP were measured during low salt intake at the end of 2 weeks. All samples were collected at 9 AM. Antigen levels were determined using a 2-site enzyme-linked immunosorbent assay.
Patients experienced significant improvement in disease related activity scores after infliximab treatment. DAS score (for rheumatoid arthritis) and BASDAI index (for ankylosing spondylitis) decreased significantly after treatment (p = 0.01 and p = 0.04 respectively). Infliximab significantly reduced the marker of inflammation (hs-CRP) (8.3 +/- 3.9 vs. 4 +/- 4.1 mg/L, p < 0.01). Plasma PAI-1 antigen (64.7 +/- 26.9 vs. 40 +/- 31.1 ng/ml, p = 0.03) and PAI-1/t-PA ratio (10.8 +/- 5.9 vs. 6.6 +/- 3.8, p = 0.02) were significantly lower after the treatment. In contrast, plasma t-PA levels were unchanged (9.4 +/- 4.4 vs. 9.0 +/- 4.3 ng/ml, p = 0.73).
This study provides evidence that TNF alpha inhibition with infliximab decreases PAI-1 Ag level and PAI-1/t-PA ratio, and hence activates fibrinolytic system in patients with chronic inflammatory disorders.
近期研究支持动脉粥样硬化存在炎症基础。患有慢性炎症性风湿性疾病的患者发生心血管事件的风险增加,这部分可归因于纤维蛋白溶解系统的抑制。英夫利昔单抗等肿瘤坏死因子α抑制剂已显示可延缓炎性关节炎的进展。在本研究中,我们调查了英夫利昔单抗对血浆纤维蛋白溶解参数的影响。
选择13例有英夫利昔单抗临床适应证的患者(7例女性,6例男性;平均年龄:44±11岁)(类风湿关节炎(RA)(n = 8),强直性脊柱炎(AS)(n = 5))。在基线低盐饮食期间测量血浆纤溶酶原激活物抑制剂(PAI-1)、组织纤溶酶原激活物(t-PA)抗原(Ag)和高敏C反应蛋白(hs-CRP)水平。所有患者均接受英夫利昔单抗(类克,静脉输注,3mg/kg)治疗。在2周结束时低盐饮食期间测量血浆PAI-1 Ag、t-PA Ag和hs-CRP。所有样本均在上午9点采集。使用双位点酶联免疫吸附测定法测定抗原水平。
英夫利昔单抗治疗后患者疾病相关活动评分有显著改善。治疗后DAS评分(用于类风湿关节炎)和BASDAI指数(用于强直性脊柱炎)显著降低(分别为p = 0.01和p = 0.04)。英夫利昔单抗显著降低炎症标志物(hs-CRP)(8.3±3.9对4±4.1mg/L,p < 0.01)。治疗后血浆PAI-1抗原(64.7±26.9对40±31.1ng/ml,p = 0.03)和PAI-1/t-PA比值(10.8±5.9对6.6±3.8,p = 0.02)显著降低。相比之下,血浆t-PA水平未改变(9.4±4.4对9.0±4.3ng/ml,p = 0.73)。
本研究提供了证据表明,用英夫利昔单抗抑制肿瘤坏死因子α可降低PAI-1 Ag水平和PAI-1/t-PA比值,从而激活慢性炎症性疾病患者的纤维蛋白溶解系统。