Department of Medicine, Karolinska Institutet, Sweden.
Lupus. 2013 Apr;22(5):477-85. doi: 10.1177/0961203313479420.
The Ro52 protein of the Ro/SSA antigen was recently defined as an E3 ligase controlling cytokine production. Autoantibodies from systemic lupus erythematosus (SLE) patients targeting the Ro52-RING domain, containing the E3 ligase activity, have been shown to inhibit the E3 ligase activity of Ro52. The objective of the present study was to investigate correlations between clinical parameters in patients with SLE and levels of Ro/SSA (Ro52 and Ro60) and La/SSB autoantibodies, including autoantibodies directed towards the functional RING and B-box domains of the Ro52 protein. SLE patients (n=232) were clinically examined and disease activity indices collected concurrently to blood sampling. The samples were analyzed for immunological parameters including autoantibodies. Ro52 autoantibody levels were associated with more variables than the other analyzed antibodies and were significantly associated with several individual items related to sSS and the diagnosis of sSS itself (p=0.004). Other associated variables were high sedimentation rate (p=0.0003), levels of immunoglobulins (p=0.0003), and an inverse correlation with levels of lymphocytes (p=0.003) and leukocytes (p=0.01). Antibodies to the RING domain of Ro52, which is the functionally active domain with E3 ligase activity, were significantly correlated with disease activity as measured by the SLAM score. We conclude that autoantibodies against Ro52 and in particular its functional RING domain are important in lupus patients and associated with several clinical and laboratory features of the disease. The impact on disease activity of Ro52-RING specific antibodies was especially noted, and could imply a functional role for these autoantibodies in inhibiting Ro52 activity, which is important for the control of proinflammatory cytokine production, including type 1 interferons.
Ro/SSA 抗原的 Ro52 蛋白最近被定义为一种控制细胞因子产生的 E3 连接酶。来自系统性红斑狼疮 (SLE) 患者的靶向 Ro52-RING 结构域的自身抗体,其中包含 E3 连接酶活性,已被证明可抑制 Ro52 的 E3 连接酶活性。本研究的目的是调查 SLE 患者的临床参数与 Ro/SSA(Ro52 和 Ro60)和 La/SSB 自身抗体水平之间的相关性,包括针对 Ro52 蛋白功能 RING 和 B-盒结构域的自身抗体。对 232 例 SLE 患者进行了临床检查,并同时采集了疾病活动指数进行血液采样。对样本进行了免疫参数分析,包括自身抗体。与其他分析的抗体相比,Ro52 自身抗体水平与更多变量相关,与与 sSS 相关的几个个体项目以及 sSS 的诊断本身显著相关(p=0.004)。其他相关变量包括高沉降率(p=0.0003)、免疫球蛋白水平(p=0.0003)以及与淋巴细胞水平呈负相关(p=0.003)和白细胞(p=0.01)。Ro52 的 RING 结构域的抗体,其是具有 E3 连接酶活性的功能活性结构域,与 SLAM 评分测量的疾病活动显著相关。我们得出结论,针对 Ro52 及其功能 RING 结构域的自身抗体在狼疮患者中很重要,与疾病的几个临床和实验室特征相关。特别注意到针对 Ro52-RING 特异性抗体的疾病活动的影响,这可能意味着这些自身抗体在抑制 Ro52 活性方面具有功能作用,这对于控制包括 1 型干扰素在内的促炎细胞因子的产生很重要。