INSERM UMR 1097, Aix Marseille Université, Parc Scientifique de Luminy, Marseille, France.
Autoimmun Rev. 2012 Sep;11(11):801-3. doi: 10.1016/j.autrev.2012.02.009. Epub 2012 Feb 12.
Rheumatoid arthritis (RA) is a chronic autoimmune disease that causes cartilage and bone destruction. The mechanisms leading to RA are unknown. There is currently no reliable cure for RA. Early treatment can reduce inflammation, joint damage and bone destruction. Thus, early diagnosis of RA is critical. However, definitive diagnosis of RA can be difficult. Immunologic tests that can be performed for the diagnosis of RA include detection of anti citrullinated protein antibodies (ACPAs). However, one third of RA patients have no ACPAs. To identify new autoantibodies in RA, we used the sera of RA patients to screen protein arrays containing 8000 human proteins. We found and validated two major autoantigens: PAD4 (peptidyl arginine deiminase 4) and BRAF (v raf murine sarcoma viral oncogene homolog B1) catalytic domain. We identified peptide targets of anti PAD4 and BRAF autoantibodies. We observed that anti PAD4 are inhibitory whereas anti BRAF stimulate BRAF activity. Anti PAD4 and anti BRAF antibodies may be used to diagnose RA, particularly in the absence of anti citrullinated protein antibodies.
类风湿关节炎(RA)是一种慢性自身免疫性疾病,可导致软骨和骨破坏。导致 RA 的机制尚不清楚。目前尚无可靠的 RA 治疗方法。早期治疗可以减轻炎症、关节损伤和骨破坏。因此,早期诊断 RA 至关重要。然而,RA 的明确诊断可能具有挑战性。可用于 RA 诊断的免疫检测包括检测抗瓜氨酸蛋白抗体(ACPAs)。然而,三分之一的 RA 患者没有 ACPAs。为了在 RA 中识别新的自身抗体,我们使用 RA 患者的血清筛选了包含 8000 个人类蛋白的蛋白质阵列。我们发现并验证了两个主要的自身抗原:肽基精氨酸脱亚氨酶 4(PAD4)和 BRAF(v raf 鼠肉瘤病毒致癌基因同源物 B1)催化结构域。我们确定了抗 PAD4 和 BRAF 自身抗体的肽靶标。我们观察到抗 PAD4 具有抑制作用,而抗 BRAF 则刺激 BRAF 活性。抗 PAD4 和抗 BRAF 抗体可用于诊断 RA,特别是在缺乏抗瓜氨酸蛋白抗体的情况下。