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Serum Clusterin as a Prognostic Marker of Chronic Spontaneous Urticaria

机译:血清簇蛋白作为慢性自发性荨麻疹的预后标志

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A substantial proportion of patients with chronic spontaneous urticaria (CSU) are refractory to antihistamines. However, identifying the subpopulation whose urticaria is not completely controlled by antihistamines remains difficult. The response of autologous serum skin test (ASST), a clinical test for the detection of basophil histamine-releasing activity upon autoantibodies or autoreactive stimulation, has been suggested as a potential predictor in the control of urticaria. We sought to identify proteins that were differentially expressed in the sera of patients with positive and negative ASST results and to investigate their association with urticaria control.Proteomics analysis was performed using sera from 3 CSU patients with positive ASST results compared with those showing negative ASST results. Seven upregulated and 5 downregulated proteins were identified by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry in the ASST-positive group compared with the ASST-negative group.Proteins that were differentially expressed according to the ASST results in CSU patients were classified into 6 groups: apolipoproteins, glycoproteins, modified albumin, haptoglobulin, plectin, and others. Among these, apolipoprotein J or clusterin was validated using an enzyme-linked immunosorbent assay. Clusterin levels in 69 ASST-positive patients were significantly higher than those in 69 ASST-negative patients and in 86 healthy controls (231.2 +/- 44.0 vs 210.2 +/- 36.1 vs 118.7 +/- 71.9g/mL, P<0.001). Furthermore, clusterin levels differed significantly between patients with responsive and refractory responses to antihistamine treatment within 3 months (231.0 +/- 39.1 vs 205.1 +/- 40.4g/mL, P<0.001). ASST results and serum clusterin levels can predict 92.7% of CSU patients whose urticaria would be refractory to antihistamines. Serum clusterin can be a prognostic marker to determine the responsiveness to antihistamine treatment in patients with CSU.
机译:慢性自发性荨麻疹(CSU)患者中相当一部分对抗组胺药难治。然而,鉴定其荨麻疹不能完全被抗组胺药控制的亚人群仍然很困难。已经提出自体血清皮肤试验(ASST)的反应是一种临床试验,用于检测自身抗体或自身反应性刺激后嗜碱性粒细胞组胺释放活性,作为控制荨麻疹的潜在预测指标。我们试图鉴定在ASST结果阳性和阴性的患者血清中差异表达的蛋白质,并研究其与荨麻疹控制的相关性。蛋白质组学分析使用3例ASST结果阳性的CSU患者血清与ASST结果阴性的患者进行蛋白质组学分析。与ASST阴性组相比,ASST阳性组通过基质辅助激光解吸/电离飞行时间质谱鉴定了7种上调蛋白和5种下调蛋白.CSU患者根据ASST结果差异表达的蛋白质分为6组:载脂蛋白,糖蛋白,修饰的白蛋白,触球蛋白,凝集素等。其中,载脂蛋白J或簇蛋白已通过酶联免疫吸附测定法进行了验证。 69名ASST阳性患者的Clusterin水平显着高于69名ASST阴性患者和86名健康对照者(231.2 +/- 44.0 vs 210.2 +/- 36.1 vs 118.7 +/- 71.9g / mL,P <0.001) 。此外,在3个月内对抗组胺药有反应和难治性反应的患者之间,簇蛋白水平差异显着(231.0 +/- 39.1 vs 205.1 +/- 40.4g / mL,P <0.001)。 ASST结果和血清簇蛋白水平可以预测92.7%的荨麻疹患者对抗组胺药耐药。血清簇蛋白可以作为确定CSU患者对抗组胺药治疗反应的预后指标。

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