Feist E, Kuckelkorn U, Dörner T, Dönitz H, Scheffler S, Hiepe F, Kloetzel P M, Burmester G R
Charité University Hospital, Humboldt University of Berlin, Germany.
Arthritis Rheum. 1999 Apr;42(4):697-702. doi: 10.1002/1529-0131(199904)42:4<697::AID-ANR12>3.0.CO;2-H.
The proteasome subunit HC9 (alpha3) has recently been identified as a major target of the humoral autoimmune response in patients with autoimmune myositis and systemic lupus erythematosus. Since B cell hyperreactivity is a common feature of systemic autoimmune diseases, patients with primary Sjögren's syndrome (SS) and other control groups were investigated to evaluate the significance of autoantibodies against the proteasome.
Analyses of autoantibodies directed against the 20S proteasome were performed using enzyme-linked immunosorbent assay, immunoblot, and 2-dimensional electrophoresis. Forty-three patients with primary SS, 47 patients with rheumatoid arthritis including 9 with secondary SS, 19 patients with gastrointestinal tumors, and 80 healthy controls were tested for antiproteasome antibodies.
Antiproteasome antibodies were detected in 39% of patients (17 of 43) with primary SS. In contrast, only 1 of 47 patients with rheumatoid arthritis showed positive reactivity (P < 0.001). Serum samples from 19 tumor patients (P < 0.003) and 80 healthy controls (P < 0.001) were serologically negative. Moreover, immunoblotting and 2-dimensional analysis of the antiproteasome response revealed a polyspecific recognition pattern in 7 patients with primary SS. Different proteasomal subunits of the alpha and beta type, including subunits that carried the proteolytic active sites, were recognized by the patients' sera.
The humoral antiproteasome response in primary SS, in contrast to its secondary form, is characterized by an extensive recognition pattern of several subunits, indicating a polyspecific B cell activation against the 20S proteasome. Moreover, proteolytically active beta-type subunits, which are important for the generation of major histocompatibility complex class I-restricted antigens, appear to be targets of the autoimmune response. The data indicate that the proteasome itself may stand on a cross point of pathways that links mechanisms of the immune defense with features of systemic autoimmunity.
蛋白酶体亚基HC9(α3)最近被确定为自身免疫性肌炎和系统性红斑狼疮患者体液自身免疫反应的主要靶点。由于B细胞反应性亢进是系统性自身免疫性疾病的一个共同特征,因此对原发性干燥综合征(SS)患者及其他对照组进行了研究,以评估抗蛋白酶体自身抗体的意义。
采用酶联免疫吸附测定、免疫印迹和二维电泳法分析针对20S蛋白酶体的自身抗体。检测了43例原发性SS患者、47例类风湿关节炎患者(包括9例继发性SS患者)、19例胃肠道肿瘤患者和80名健康对照者的抗蛋白酶体抗体。
在39%(43例中的17例)的原发性SS患者中检测到抗蛋白酶体抗体。相比之下,47例类风湿关节炎患者中只有1例呈阳性反应(P<0.001)。19例肿瘤患者(P<0.003)和80名健康对照者(P<0.001)的血清样本在血清学上呈阴性。此外,对抗蛋白酶体反应的免疫印迹和二维分析显示,7例原发性SS患者存在多特异性识别模式。患者血清识别了α型和β型不同的蛋白酶体亚基,包括带有蛋白水解活性位点的亚基。
与继发性SS不同,原发性SS中的体液抗蛋白酶体反应的特征是对几个亚基具有广泛的识别模式,表明针对20S蛋白酶体存在多特异性B细胞激活。此外,对主要组织相容性复合体I类限制性抗原的产生很重要的具有蛋白水解活性的β型亚基似乎是自身免疫反应的靶点。数据表明,蛋白酶体本身可能处于将免疫防御机制与系统性自身免疫特征联系起来的途径的交叉点上。