Yang Chun-hua, Huang Feng, Deng Xiao-hu, Zhang Jiang-lin, Zhang Li-yun, Guo Jun-hua, Liang Dong-feng, Wang Li-sha, Zhang Ya-mei
Department of Rheumatology, General Hospital of Chinese People's Liberation Army, Beijing, China.
Zhonghua Yi Xue Za Zhi. 2006 Sep 19;86(35):2451-4.
To evaluate the effect of Infliximab and Etanercept two types of anti-tumor necrosis factor-alpha (TNF-alpha) inhibitors, on the serum level of matrix metalloproteinase 3 (MMP-3) in the pathogenesis of ankylosing spondylitis (AS).
47 patients with AS, 40 males and 7 females, aged 17 - 51, were treated with Infliximab (5 mg/kg i.v at weeks 0, 2, and 6); and 26 patients with AS were treated with Etanercept (25 mg, twice a week for 12 weeks). Clinical data including Bath AS indices (BASDAI and BASFI) and sera were collected at baseline and other different times. Erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP) were measured. Serum levels of MMP-3 were measured with MMP-3 ELISA kits.
Two, six, and ten weeks after Infliximab treatment the levels of ESR, CRP, and serum MMP-3 of the AS patients were all significantly lower than the baseline level (all P < 0.01), and the serum MMP-3 levels were all significantly correlated with ESR (all P < 0.05). In the Etanercept group 1, 2, 4, 8, and 12 weeks after treatment the levels of serum MMP-3, ESR, CRP, BASDAI, and BASFI were all significantly lower than the baseline levels (all P < 0.01); before the treatment ESR was significantly correlated with CRP (r = 0.80, P < 0.01), BASDAI was significantly correlated with BASFI (r = 0.48, P < 0.05), and MMP-3 was significantly correlated with ESR (r = 0.74, P < 0.01) and with CRP (r = 0.72, P < 0.01); and 12 weeks after the treatment significant correlation still existed between ESR and CRP (r = 0.40, P < 0.05), BASDAI and BASFI (r = 0.89, P < 0.01), and MMP-3 and ESR (r = 0.43, P = 0.029), however, there was no significant correlation between CRP and serum level of MMP-3 (r = 0.37, P = 0.061).
Infliximab and Etanercept, 2 anti-TNF-alpha inhibitors, not only significantly decrease the ESR and CRP, but also decrease the serum level of MMP-3 of patients with AS. MMP-3 is involved in the pathogenesis and disease activity of AS. MMP-3 is also a potentially useful marker of AS disease activity and useful parameter to assess the effectiveness of anti-TNF-alpha inhibitor in treatment of AS.
评估英夫利昔单抗和依那西普这两种抗肿瘤坏死因子-α(TNF-α)抑制剂对强直性脊柱炎(AS)发病机制中基质金属蛋白酶3(MMP-3)血清水平的影响。
47例AS患者,男40例,女7例,年龄17 - 51岁,接受英夫利昔单抗治疗(第0、2和6周静脉注射5 mg/kg);26例AS患者接受依那西普治疗(25 mg,每周两次,共12周)。在基线及其他不同时间收集包括巴斯强直性脊柱炎指数(BASDAI和BASFI)在内的临床数据和血清。检测红细胞沉降率(ESR)和C反应蛋白(CRP)。用MMP-3 ELISA试剂盒检测血清MMP-3水平。
英夫利昔单抗治疗2周、6周和10周后,AS患者的ESR、CRP和血清MMP-3水平均显著低于基线水平(均P < 0.01),且血清MMP-3水平均与ESR显著相关(均P < 0.05)。依那西普组治疗1周、2周、4周、8周和12周后,血清MMP-3、ESR、CRP、BASDAI和BASFI水平均显著低于基线水平(均P < 0.01);治疗前ESR与CRP显著相关(r = 0.80,P < 0.01),BASDAI与BASFI显著相关(r = 0.48,P < 0.05),MMP-3与ESR显著相关(r = 0.74,P < 0.01)且与CRP显著相关(r = 0.72,P < 0.01);治疗12周后ESR与CRP仍存在显著相关性(r = 0.40,P < 0.05),BASDAI与BASFI显著相关(r = 0.89,P < 0.01),MMP-3与ESR显著相关(r = 0.43,P = 0.029),然而,CRP与血清MMP-3水平之间无显著相关性(r = 0.37,P = 0.061)。
英夫利昔单抗和依那西普这两种抗TNF-α抑制剂不仅能显著降低AS患者的ESR和CRP,还能降低其血清MMP-3水平。MMP-3参与AS的发病机制和疾病活动。MMP-3也是AS疾病活动的一个潜在有用标志物以及评估抗TNF-α抑制剂治疗AS有效性的有用参数。