Kurowska Weronika, Kuca-Warnawin Ewa H, Radzikowska Anna, Maśliński Włodzimierz
National Institute of Geriatrics, Rheumatology and Rehabilitation, Warsaw, Poland.
Cent Eur J Immunol. 2017;42(4):390-398. doi: 10.5114/ceji.2017.72807. Epub 2017 Dec 30.
The most specific autoimmunity known for rheumatoid arthritis (RA) is reflected by generation of anti-citrullinated protein antibodies (ACPA). Presence of ACPA in established RA is associated with disease severity, while generation of ACPA at early developmental phases of RA can have a strong predictive value for progressing to the full-blown disease. Hence, development of ACPA may be of crucial importance to the pathogenesis of RA. Therefore, a lot of effort has been put recently to investigate the feature of ACPA at early developmental stages of RA (before disease onset) and functional activities of these autoantibodies. Results of these studies enlarged the knowledge about the nature of ACPA, which is essential for planning the therapeutic or preventive strategies interfering with their development and pathogenic functions. In this review we describe recent evidence for a role of ACPA in the etiopathogenesis of RA and indicate key unresolved issues regarding ACPA biology that need to be clarified in the future.
类风湿关节炎(RA)最为明确的自身免疫表现是抗瓜氨酸化蛋白抗体(ACPA)的产生。在已确诊的RA中,ACPA的存在与疾病严重程度相关,而在RA早期发展阶段ACPA的产生对疾病进展至全面发作具有很强的预测价值。因此,ACPA的产生可能对RA的发病机制至关重要。因此,最近人们付出了很多努力来研究RA早期发展阶段(疾病发作前)ACPA的特征以及这些自身抗体的功能活性。这些研究结果扩展了我们对ACPA性质的认识,这对于制定干扰其产生和致病功能的治疗或预防策略至关重要。在本综述中,我们描述了ACPA在RA发病机制中作用的最新证据,并指出了关于ACPA生物学仍未解决的关键问题,这些问题有待未来阐明。