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首页> 外文期刊>International journal of rheumatic diseases >Serum proteome analysis in patients with rheumatoid arthritis receiving therapy with etanercept, a chimeric tumor necrosis factor-alpha receptor.
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Serum proteome analysis in patients with rheumatoid arthritis receiving therapy with etanercept, a chimeric tumor necrosis factor-alpha receptor.

机译:接受依那西普治疗的类风湿关节炎患者的血清蛋白质组学分析。依那西普是一种嵌合的肿瘤坏死因子-α受体。

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摘要

Rheumatoid arthritis (RA) is a chronic inflammatory disorder of the synovium resulting in the destruction of affected joint cartilage and bone structures. Etanercept is a biological agent that blocks the tumor necrosis factor-α (TNF-α)-mediated inflammatory processes in RA patients, and has a regenerative effect on cartilage. In order to identify novel disease-related proteins and candidate biomarkers, we performed proteomic profiling of the serum in patients with RA who were treated with etanercept.Serum samples were obtained from eight RA patients before and after etanercept treatment. The low molecular weight proteins in the serum were concentrated and analyzed by liquid chromatography-tandem mass spectrometry. The results before and after etanercept treatment were compared by the spectrum count method.Among a total of 477 proteins identified, 12 were found to be decreased and five were increased by etanercept treatment. Some of the changed proteins were known to be related to RA, and most of the other changed proteins may play possible roles in the TNF-α signaling pathway or the state of cartilage and extracellular matrix.The present proteomic study identified several proteins that could be involved in the pathogenesis of RA. These findings could thus lead to the identification of novel candidate disease-related protein biomarkers for RA, or indicate new targets for therapy.
机译:类风湿关节炎(RA)是一种滑膜的慢性炎症性疾病,会导致关节软骨和骨骼结构的破坏。 Etanercept是一种生物制剂,可阻断RA患者中肿瘤坏死因子-α(TNF-α)介导的炎症过程,并对软骨具有再生作用。为了鉴定与疾病相关的新蛋白和候选生物标志物,我们对接受依那西普治疗的RA患者进行了蛋白质组学分析,并从依那西普治疗前后的8位RA患者中获取了血清样本。浓缩血清中的低分子量蛋白质,并通过液相色谱-串联质谱法进行分析。通过光谱计数法比较了依那西普治疗前后的结果。在鉴定出的477种蛋白质中,依那西普处理减少了12种蛋白质,增加了5种。已知某些改变的蛋白质与RA相关,而大多数其他改变的蛋白质可能在TNF-α信号通路或软骨和细胞外基质的状态中可能发挥作用。本蛋白质组学研究确定了几种可能与RA相关的蛋白质。参与RA的发病机制。因此,这些发现可能导致针对RA的新的候选疾病相关蛋白质生物标记物的鉴定,或表明新的治疗靶标。

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