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S100 蛋白与风湿性疾病。

S100 proteins in rheumatic diseases.

机构信息

Institute of Immunology, University Hospital Münster, Münster, Germany.

Department of Otorhinolaryngology, Head and Neck Surgery, University Hospital Münster, Münster, Germany.

出版信息

Nat Rev Rheumatol. 2018 Sep;14(9):528-541. doi: 10.1038/s41584-018-0058-9.

Abstract

Rheumatic diseases are characterized by sterile inflammation that causes severe long-term damage to various organ systems. A growing body of evidence supports a pivotal role for the pro-inflammatory calcium-binding S100 family of proteins in the pathogenesis of rheumatic diseases. Some S100 proteins are released at the site of inflammation and act as danger-associated molecular pattern molecules by activating pattern recognition receptors. Increased concentrations of S100 proteins in serum and synovial fluid closely correlate with disease activity in several rheumatic diseases and serve as useful biomarkers for monitoring disease activity. Some S100 proteins are also valid biomarkers for predicting response to treatment, systemic organ involvement or disease flares in rheumatic diseases. Analyses of knockout mouse models have confirmed a functional role for S100 proteins, particularly S100A8 and S100A9, in rheumatic diseases, indicating that blocking the expression, release or function of these proteins might be an innovative therapeutic strategy. Owing to their local pattern of expression, specific mechanism of release and autoregulatory effects, such therapeutic approaches would primarily target the local inflammatory process and present only minor risks of systemic adverse effects.

摘要

风湿性疾病的特征是无菌性炎症,可导致多种器官系统的严重长期损害。越来越多的证据支持促炎钙结合 S100 蛋白家族在风湿性疾病发病机制中的关键作用。一些 S100 蛋白在炎症部位释放,并通过激活模式识别受体作为危险相关分子模式分子起作用。几种风湿性疾病中血清和滑液中 S100 蛋白浓度的增加与疾病活动密切相关,可作为监测疾病活动的有用生物标志物。一些 S100 蛋白也是预测风湿性疾病治疗反应、全身器官受累或疾病发作的有效生物标志物。敲除小鼠模型的分析证实了 S100 蛋白(尤其是 S100A8 和 S100A9)在风湿性疾病中的功能作用,表明阻断这些蛋白的表达、释放或功能可能是一种创新的治疗策略。由于其局部表达模式、特定的释放机制和自身调节作用,这种治疗方法主要针对局部炎症过程,且仅有较小的全身不良反应风险。

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