Department of Cell and Molecular Biology, Uppsala University, SE-75124, Uppsala, Sweden.
J Clin Immunol. 2012 Jun;32(3):540-50. doi: 10.1007/s10875-012-9657-4. Epub 2012 Feb 11.
The progress in identifying immunological mechanisms in juvenile idiopathic arthritis (JIA) has partly been hampered by the fact that the disease is heterogeneous. Here we have investigated complement and Fc receptors, as part of the inflammatory process, in two subgroups of JIA.
Blood from 26 patients with oligoarticular or polyarticular course type JIA and 21 healthy age and sex-matched controls were investigated by FACS and immunoassays.
Increased numbers of monocytes and augmented plasma levels of C-reactive protein, C3a and IgG were found in both JIA subgroups. However, only polyarticular patients exhibited increased expression of Fc gamma receptor (FcγR) II and III and complement receptor (CR) 1 on monocytes along with enhanced CR1 expression on B cells. A correlation was observed between degree of receptor expression and C3a levels in the patients.
Complement and Fc receptors are up regulated in children with multiple joint involvements, thus highlighting these pathways in the pathogenesis of polyarticular JIA.
儿童特发性关节炎(JIA)的免疫学机制研究进展受到疾病异质性的阻碍。本研究旨在探讨 JIA 两种亚型中补体和 Fc 受体(炎症反应的一部分)。
流式细胞术和免疫测定法检测 26 例少关节型或多关节型 JIA 患者和 21 名年龄和性别匹配的健康对照者的血液。
两个 JIA 亚组的单核细胞数量增加,C 反应蛋白、C3a 和 IgG 血浆水平升高。然而,只有多关节型患者的单核细胞上 FcγR II 和 III 以及 CR1 的表达增加,B 细胞上的 CR1 表达增强。患者的受体表达程度与 C3a 水平之间存在相关性。
多关节型 JIA 患儿的补体和 Fc 受体表达上调,提示这些通路在其发病机制中发挥作用。