Lee Adrian Y S, Bannan Jennifer L, Adams Murray J, Körner Heinrich
Western Health, Melbourne, Victoria, Australia.
School of Medicine, University of Tasmania, Hobart, Tasmania, Australia.
Clin Rheumatol. 2017 Jun;36(6):1453-1456. doi: 10.1007/s10067-017-3652-3. Epub 2017 Apr 25.
B cells are known to play a dominant pathogenic role in autoimmune conditions such as systemic lupus erythematosus (SLE) and rheumatoid arthritis. In recent times, the chemokine receptor CCR6 and its cognate ligand CCL20 have been shown to play a role in the fundamental kinetics of germinal centres and B cell responses. As CCR6 is found on B cells and is upregulated after activation, we investigated the expression of CCR6 on naive, pre-germinal centre (GC), GC/plasma cell and memory B cells in peripheral B cells of SLE patients and healthy controls using flow cytometry. Pre-germinal centre B cells are found in lower proportions and the expression of CCR6 is increased on B cells of SLE patients, suggesting a role for the chemokine pair in the pathogenesis of the disease. Further studies are needed to explore these preliminary results.
已知B细胞在自身免疫性疾病(如系统性红斑狼疮和类风湿性关节炎)中起主要致病作用。近年来,趋化因子受体CCR6及其同源配体CCL20已被证明在生发中心的基本动力学和B细胞反应中发挥作用。由于CCR6存在于B细胞上且在激活后上调,我们使用流式细胞术研究了SLE患者和健康对照外周B细胞中幼稚、生发前中心(GC)、GC/浆细胞和记忆B细胞上CCR6的表达。生发前中心B细胞的比例较低,且SLE患者B细胞上CCR6的表达增加,这表明该趋化因子对在疾病发病机制中起作用。需要进一步研究来探索这些初步结果。