Kang Kwi Young, Woo Jung-Won, Park Sung-Hwan
Division of Rheumatology, Department of Internal Medicine, The Catholic University of Korea College of Medicine, Seoul, Korea. ; Division of Rheumatology, Department of Internal Medicine, Incheon St. Mary's Hospital, The Catholic University of Korea College of Medicine, Incheon, Korea.
Department of Convergent Research Consortium for Immunologic Disease, Seoul St. Mary's Hospital, The Catholic University of Korea College of Medicine, Seoul, Korea. ; Business Development, Genexine Inc., Seongnam, Korea.
Korean J Intern Med. 2014 Jan;29(1):12-9. doi: 10.3904/kjim.2014.29.1.12. Epub 2014 Jan 2.
S100A8 and S100A9 are major leukocyte proteins, known as damage-associated molecular patterns, found at high concentrations in the synovial fluid of patients with rheumatoid arthritis (RA). A heterodimeric complex of S100A8/A9 is secreted by activated leukocytes and binds to Toll-like receptor 4, which mediates downstream signaling and promotes inflammation and autoimmunity. Serum and synovial fluid levels of S100A8/A9 are markedly higher in patients with RA than in patients with osteoarthritis or miscellaneous inflammatory arthritis. Serum levels of S100A8/A9 are significantly correlated with clinical and laboratory markers of inflammation, such as C-reactive protein, erythrocyte sedimentation rate, rheumatoid factor, and the Disease Activity Score for 28 joints. Significant correlations have also been found between S100A8/A9 and radiographic and clinical assessments of joint damage, such as hand radiographs and the Rheumatoid Arthritis Articular Damage score. In addition, among known inflammatory markers, S100A8/A9 has the strongest correlation with total sum scores of ultrasonography assessment. Furthermore, baseline levels of S100A8/A9 are independently associated with progression of joint destruction in longitudinal studies and are responsive to change during conventional and biologic treatments. These findings suggest S100A8/A9 to be a valuable diagnostic and prognostic biomarker for RA.
S100A8和S100A9是主要的白细胞蛋白,被称为损伤相关分子模式,在类风湿性关节炎(RA)患者的滑液中浓度很高。S100A8/A9异二聚体复合物由活化的白细胞分泌,并与Toll样受体4结合,后者介导下游信号传导并促进炎症和自身免疫。RA患者血清和滑液中S100A8/A9水平明显高于骨关节炎或其他炎症性关节炎患者。S100A8/A9的血清水平与炎症的临床和实验室指标显著相关,如C反应蛋白、红细胞沉降率、类风湿因子以及28个关节的疾病活动评分。在S100A8/A9与关节损伤的影像学和临床评估之间也发现了显著相关性,如手部X线片和类风湿性关节炎关节损伤评分。此外,在已知的炎症标志物中,S100A8/A9与超声检查评估的总分相关性最强。此外,在纵向研究中,S100A8/A9的基线水平与关节破坏的进展独立相关,并且在传统治疗和生物治疗期间对变化有反应。这些发现表明S100A8/A9是RA一种有价值的诊断和预后生物标志物。