Petrovská Nora, Prajzlerová Klára, Vencovský Jiří, Šenolt Ladislav, Filková Mária
Institute of Rheumatology and Department of Rheumatology, 1st Faculty of Medicine, Charles University in Prague, Czech Republic.
Institute of Rheumatology and Department of Rheumatology, 1st Faculty of Medicine, Charles University in Prague, Czech Republic.
Autoimmun Rev. 2021 May;20(5):102797. doi: 10.1016/j.autrev.2021.102797. Epub 2021 Mar 18.
Rheumatoid arthritis (RA) is a chronic autoimmune disease considered as a multistep process spanning from the interaction of genetic (e.g., shared epitope or non-HLA loci), environmental and behavioral risk factors (e.g., smoking) leading to breaking immune tolerance and autoimmune processes such as the production of autoantibodies (e.g., antibodies against citrullinated proteins ACPA or rheumatoid factors, RF), development of the first symptoms without clinical arthritis, and, finally, the manifestation of arthritis. Despite the typical joint involvement in established RA, the pathogenesis of the disease likely begins far from joint structures: in the lungs or periodontium in association with citrullination, intestinal microbiome, or adipose tissue, which supports normal findings in synovial tissue in ACPA+ patients with arthralgia. The presence of ACPA is detectable even years before the first manifestation of RA. The pre-clinical phase of RA is the period preceding clinically apparent RA with ACPA contributing to the symptoms without subclinical inflammation. While the combination of ACPA and RF increases the risk of progression to RA by up to 10 times, increasing numbers of novel autoantibodies are to be investigated to contribute to the increased risk and pathogenesis of RA. With growing knowledge about the course of RA, new aspiration emerges to cure and even prevent RA, shifting the "window of opportunity" to the pre-clinical phases of RA. The clinical definition of individuals at risk of developing RA (clinically suspect arthralgia, CSA) makes it possible to unify these at-risk individuals' clinical characteristics for "preventive" treatment in ongoing clinical trials using mostly biological or conventional synthetic disease-modifying drugs. However, the combination of symptoms, laboratory, and imaging biomarkers may be the best approach to select the correct target at-risk population. The current review aims to explore different phases of RA and discuss the potential of (non)pharmacological intervention aiming to prevent RA.
类风湿关节炎(RA)是一种慢性自身免疫性疾病,被认为是一个多步骤过程,涵盖遗传(如共享表位或非HLA基因座)、环境和行为风险因素(如吸烟)的相互作用,导致免疫耐受破坏和自身免疫过程,如自身抗体(如抗瓜氨酸化蛋白抗体ACPA或类风湿因子RF)的产生、无临床关节炎的首发症状的出现,以及最终关节炎的表现。尽管在已确诊的RA中典型的关节受累情况较为常见,但该疾病的发病机制可能始于远离关节结构的部位:与瓜氨酸化、肠道微生物群或脂肪组织相关的肺部或牙周组织,这支持了ACPA阳性且有关节痛的患者滑膜组织的正常表现。ACPA甚至在RA首次表现出现前数年就可检测到。RA的临床前期是指临床明显的RA出现之前的时期,ACPA在无亚临床炎症的情况下导致症状出现。虽然ACPA和RF的联合使进展为RA的风险增加多达10倍,但越来越多的新型自身抗体有待研究,以探讨其在RA风险增加和发病机制中的作用。随着对RA病程的认识不断增加,出现了治愈甚至预防RA的新愿望,将“机会窗口”转移到RA的临床前期阶段。对有发展为RA风险的个体(临床疑似关节痛,CSA)的临床定义,使得在正在进行的临床试验中能够统一这些高危个体的临床特征,以便使用主要是生物或传统合成的改善病情药物进行“预防性”治疗。然而,症状、实验室和影像生物标志物的联合可能是选择正确的高危目标人群的最佳方法。本综述旨在探讨RA的不同阶段,并讨论旨在预防RA的(非)药物干预的潜力。