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基质金属蛋白酶-3的活性形式是炎症性关节疾病中滑膜炎症和软骨更新的标志物。

The active form of MMP-3 is a marker of synovial inflammation and cartilage turnover in inflammatory joint diseases.

作者信息

Sun Shu, Bay-Jensen Anne-Christine, Karsdal Morten A, Siebuhr Anne Sofie, Zheng Qinlong, Maksymowych Walter P, Christiansen Thorbjørn G, Henriksen Kim

机构信息

Nordic Bioscience Biomarkers and Research, Herlev, Denmark.

出版信息

BMC Musculoskelet Disord. 2014 Mar 19;15:93. doi: 10.1186/1471-2474-15-93.

Abstract

BACKGROUND

Matrix metalloproteinase-3 (MMP-3) plays an important role in the pathology of rheumatoid arthritis (RA) and ankylosing spondylitis (AS). Measurement of active MMP-3 in clinical samples could provide information about progression of rheumatoid diseases, and potentially response to treatment. Hence, we aimed to develop a sensitive assay specifically measuring the active form of MMP-3 (act-MMP-3) both in ex vivo models and in human sera.

METHODS

A monoclonal antibody against the first 6 amino acids of act-MMP-3 was developed, and the specificity was carefully tested by comparing total and active MMP-3. A technically robust act-MMP-3 ELISA was produced. For biological validation, human synovial membrane and human cartilage explant (HEX) culture models were measured and compared by ELISA and immunoblots. For clinical relevance, the serum levels of act-MMP-3 in AS and RA patients before and after anti-TNF-α treatment were evaluated.

RESULTS

A highly specific and technically robust ELISA detecting act-MMP-3 in serum was developed. The lower limit of detection was 33.7 pg/mL. The dilution and spiking recovery of human serum was within 100 ± 20%. The average intra- and inter-assay variations were 3.1% and 13.5% respectively.High levels of act-MMP-3 expression were observed in human synovial membrane culture and oncostatin M and TNF-α stimulated human cartilage. In a cross-sectional study of both AS and RA patients, serum act-MMP-3 level was correlated with C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR). In addition, in patients receiving anti-TNF-α treatment, the serum level of act-MMP-3 was significantly reduced compared to baseline level reflecting the anti-inflammatory effects of the treatment.

CONCLUSION

We have successfully developed an assay measuring act-MMP-3 in human serum showing correlation to inflammatory markers. Further studies are required to clarify, whether act-MMP-3 can serve as a predictive marker for outcome in chronic rheumatoid disorders.

摘要

背景

基质金属蛋白酶-3(MMP-3)在类风湿关节炎(RA)和强直性脊柱炎(AS)的病理过程中起重要作用。检测临床样本中的活性MMP-3可为类风湿疾病的进展及潜在的治疗反应提供信息。因此,我们旨在开发一种灵敏的检测方法,专门用于在体外模型和人血清中检测活性形式的MMP-3(act-MMP-3)。

方法

制备了一种针对act-MMP-3前6个氨基酸的单克隆抗体,并通过比较总MMP-3和活性MMP-3仔细测试了其特异性。建立了一种技术稳健的act-MMP-3酶联免疫吸附测定法(ELISA)。为进行生物学验证,通过ELISA和免疫印迹法对人滑膜和人软骨外植体(HEX)培养模型进行检测和比较。为评估临床相关性,对AS和RA患者在抗TNF-α治疗前后的血清act-MMP-3水平进行了评估。

结果

开发出一种高度特异且技术稳健的ELISA法,用于检测血清中的act-MMP-3。检测下限为33.7 pg/mL。人血清的稀释和加标回收率在100±20%以内。平均批内和批间变异分别为3.1%和13.5%。在人滑膜培养物以及抑瘤素M和TNF-α刺激的人软骨中观察到高水平的act-MMP-3表达。在一项针对AS和RA患者的横断面研究中,血清act-MMP-3水平与C反应蛋白(CRP)和红细胞沉降率(ESR)相关。此外,在接受抗TNF-α治疗的患者中,血清act-MMP-3水平与基线水平相比显著降低,反映了该治疗的抗炎作用。

结论

我们成功开发了一种检测人血清中act-MMP-3的方法,该方法与炎症标志物相关。需要进一步研究以阐明act-MMP-3是否可作为慢性类风湿疾病预后的预测标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c1f/4003863/2525d9ba7859/1471-2474-15-93-1.jpg

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