Department of Biomedical Engineering, University of Houston, Houston, TX, 77204-5060, USA.
Center for Clinical Studies, Webster, TX, 77598, USA.
Proteomics Clin Appl. 2020 Mar;14(2):e1800114. doi: 10.1002/prca.201800114. Epub 2019 Dec 11.
Psoriasis is a complex immunological skin disease. However, whether humoral autoimmunity is involved in the pathogenesis of psoriasis remains unclear. The aim is to determine if there are autoantibodies associated with disease activity of psoriasis.
A novel autoantigen array harboring 75 antigens is developed to discover autoantibodies in the serum of psoriasis patients (N = 12) compared to healthy controls (N = 12). Validation studies are performed in a larger cohort of psoriasis patients (N = 73) and healthy controls (N = 75) together with atopic dermatitis as disease controls (N = 10).
The screening results demonstrate that immunoglobulin G4 (IgG4) anti-gliadin autoantibodies are significantly elevated in the serum of psoriasis patients, compared to healthy controls. Receiver operating characteristic (ROC) analysis indicates that IgG4 anti-gliadin autoantibody levels can clearly discriminate psoriasis patients from healthy controls with an AUC of 0.98 (p < 0.001). Also, IgG4 anti-gliadin autoantibody can reflect disease severity with the psoriasis area severity index score in a subpopulation of psoriasis patients.
These results suggest that IgG4 anti-gliadin autoantibody may be a disease marker of psoriasis, and it may be useful in clinical diagnostics and disease monitoring of psoriasis.
This work represents a relatively comprehensive screening of autoantibodies, that is, IgG4 autoantibodies in psoriasis using an in-house autoantigen array. This novel proteomic platform may be useful in clinical screening of IgG type or IgG4 subtype autoantibodies in psoriasis patients for disease monitoring or drug responses. Particularly, IgG4 anti-gliadin autoantibody, as a new potential disease marker of psoriasis, may be useful in clinical diagnostics or prognostics of related immunological disorders.
银屑病是一种复杂的免疫性皮肤病。然而,体液自身免疫是否参与银屑病的发病机制尚不清楚。本研究旨在确定是否存在与银屑病疾病活动相关的自身抗体。
开发了一种新型的自身抗原阵列,其中包含 75 种抗原,用于发现银屑病患者(N=12)与健康对照者(N=12)血清中的自身抗体。在更大的银屑病患者队列(N=73)和健康对照者(N=75)以及特应性皮炎作为疾病对照者(N=10)中进行验证研究。
筛选结果表明,与健康对照者相比,银屑病患者血清中免疫球蛋白 G4(IgG4)抗麦胶蛋白自身抗体明显升高。受试者工作特征(ROC)分析表明,IgG4 抗麦胶蛋白自身抗体水平可清晰地区分银屑病患者与健康对照者,AUC 为 0.98(p<0.001)。此外,在银屑病患者亚群中,IgG4 抗麦胶蛋白自身抗体水平可反映疾病严重程度与银屑病面积严重指数评分。
这些结果表明,IgG4 抗麦胶蛋白自身抗体可能是银屑病的疾病标志物,可能有助于银屑病的临床诊断和疾病监测。
本工作代表了使用内部自身抗原阵列对银屑病自身抗体(即 IgG4 自身抗体)进行的相对全面的筛选。该新型蛋白质组学平台可能有助于临床筛选银屑病患者 IgG 型或 IgG4 亚型自身抗体,用于疾病监测或药物反应。特别是,IgG4 抗麦胶蛋白自身抗体作为一种新的潜在银屑病疾病标志物,可能有助于相关免疫性疾病的临床诊断或预后。