Klareskog Lars, Rönnelid Johan, Lundberg Karin, Padyukov Leonid, Alfredsson Lars
Rheumatology Unit, Department of Medicine, Karolinska Institutet/Karolinska University Hospital, SE-171 76, Stockholm, Sweden.
Annu Rev Immunol. 2008;26:651-75. doi: 10.1146/annurev.immunol.26.021607.090244.
Antibodies to citrullinated proteins (ACPA), i.e., to peptides posttranslationally modified by the conversion of arginine to citrulline, are specific serological markers for rheumatoid arthritis (RA). Studies on anticitrulline immunity, summarized in this review, demonstrate that the criterion-based syndrome RA should be subdivided into at least two distinct subsets (ACPA-positive and ACPA-negative disease). A new etiological model is proposed for ACPA-positive RA, built on MHC class II-dependent activation of adaptive immunity. Fundamentals of this model include the following: (a) ACPA antedate onset of arthritis; (b) ACPA may aggravate arthritis in rodents; (c) ACPA are triggered in the context of genes that confer susceptibility to RA (HLA-DRB1 SE) and by environmental agents triggering RA (smoking or bacterial stimuli); (d) ACPA may complex with citrullinated proteins present in target tissue as part of a multistep process for arthritis development. The model provides a new basis for molecular studies on the pathogenesis of ACPA-positive arthritis.
抗瓜氨酸化蛋白抗体(ACPA),即针对经精氨酸向瓜氨酸转化后进行翻译后修饰的肽段的抗体,是类风湿关节炎(RA)的特异性血清学标志物。本综述中总结的关于抗瓜氨酸免疫的研究表明,基于标准的综合征RA应至少细分为两个不同的亚组(ACPA阳性和ACPA阴性疾病)。本文提出了一种针对ACPA阳性RA的新病因模型,该模型基于MHC II类依赖性适应性免疫激活。该模型的基本要点如下:(a)ACPA早于关节炎发病;(b)ACPA可能加重啮齿动物的关节炎;(c)ACPA在赋予RA易感性的基因(HLA - DRB1 SE)背景下以及由引发RA的环境因素(吸烟或细菌刺激)触发;(d)作为关节炎发展多步骤过程的一部分,ACPA可能与靶组织中存在的瓜氨酸化蛋白形成复合物。该模型为ACPA阳性关节炎发病机制的分子研究提供了新的基础。