Cui Li, Elzakra Naseim, Xu Shuaimei, Xiao Gary Guishan, Yang Yan, Hu Shen
UCLA School of Dentistry, Los Angeles, CA 90095, USA.
UCLA Jonsson Comprehensive Cancer Center, Los Angeles, CA 900953, USA.
Oncotarget. 2017 May 2;8(18):30039-30049. doi: 10.18632/oncotarget.15613.
Primary Sjögren's syndrome (pSS) is a chronic autoimmune disease which might progress to mucosal-associated lymphoid tissue lymphoma (pSS/MALT). Diagnosis of pSS requires an invasive tissue biopsy and a delay in diagnosis of pSS has been frequently reported. In this study, four proteins including cofilin-1, alpha-enolase, annexin A2 and Rho GDP-dissociation inhibitor 2 (RGI2) were found to be over-expressed in pSS and pSS/MALT by 2D gel electrophoresis/mass spectrometry, and the finding was verified by the microarray analysis and western blotting results. We then developed enzyme-linked immunosorbent assays for autoantibodies including anti-cofilin-1, anti-alpha-enolase and anti-RGI2 with good quantitative ability. The expression levels of salivary anti-cofilin-1, anti-alpha-enolase and anti-RGI2 were found to be the highest in pSS/MALT patients and lowest in healthy controls. The combination of these three antiantibodies yielded an "area under the curve" (AUC) value of 0.94 with an 86% sensitivity and 93% specificity in distinguishing patients with pSS from healthy controls, an AUC value of 0.99 with a 95% sensitivity and 94% specificity in distinguishing patients with pSS/MALT from healthy controls and an AUC value of 0.86 with a 75% sensitivity and 94% specificity in distinguishing pSS/MALT patients from pSS patients. Collectively, we have successfully identified a panel of potential autoantigens that are progressively up-regulated during the development of pSS and its progression to MALT lymphoma. The autoantibody biomarkers may be used to help diagnose pSS and predict its progression to MALT lymphoma.
原发性干燥综合征(pSS)是一种慢性自身免疫性疾病,可能会进展为黏膜相关淋巴组织淋巴瘤(pSS/MALT)。pSS的诊断需要进行侵入性组织活检,且经常有关于pSS诊断延迟的报道。在本研究中,通过二维凝胶电泳/质谱法发现,包括丝切蛋白-1、α-烯醇化酶、膜联蛋白A2和Rho GDP解离抑制剂2(RGI2)在内的四种蛋白质在pSS和pSS/MALT中过表达,这一发现通过微阵列分析和蛋白质印迹结果得到了验证。然后,我们开发了针对抗丝切蛋白-1、抗α-烯醇化酶和抗RGI2等自身抗体的酶联免疫吸附测定法,具有良好的定量能力。发现唾液中抗丝切蛋白-1、抗α-烯醇化酶和抗RGI2的表达水平在pSS/MALT患者中最高,在健康对照中最低。这三种自身抗体的组合在区分pSS患者与健康对照时,“曲线下面积”(AUC)值为0.94,灵敏度为86%,特异性为93%;在区分pSS/MALT患者与健康对照时,AUC值为0.99,灵敏度为95%,特异性为94%;在区分pSS/MALT患者与pSS患者时,AUC值为0.86,灵敏度为75%,特异性为94%。总体而言,我们成功鉴定出一组潜在的自身抗原,它们在pSS发展及其向MALT淋巴瘤进展过程中逐渐上调。这些自身抗体生物标志物可用于帮助诊断pSS并预测其向MALT淋巴瘤的进展。