Kimpel Donald, Dayton Tim, Kannan Krishnaswamy, Wolf Robert E
Department of Medicine, Center of Excellence of Rheumatology and Arthritis, LSU Health Sciences Center, Shreveport, Louisiana 71130, USA.
Inflammation. 2003 Apr;27(2):59-70. doi: 10.1023/a:1023215515617.
Rheumatoid arthritis (RA) is a common systemic inflammatory disease thought to be T-helper-1 cell driven, though current controversy involves the relative role of T cells versus other leukocytes. Thus, there is a need for better understanding of the role of various leukocytes and their subsets in RA. Using the streptococcal cell wall (SCW) induced arthritis model, we examined leukocytes isolated from peripheral blood, spleen, and lymph nodes using monoclonal antibodies directed against lineage specific cell surface markers. Activation status of these cells was assessed using CD44 and CD71 as markers. T cells in general, and CD4+ T cells in particular were found to be activated in spleen and lymph nodes. B cells and monocytes in spleen demonstrated increased activation as well. The activation of cells in the myeloid and lymphoid lineages in the chronic phase of arthritis indicates ongoing involvement of innate and cognate immunity. This study quantitates specific changes in B and T lymphocytes, and myeloid cells and is consistent with findings in human RA in which specific antibodies, T cells, and myeloid cells are all implicated in the pathogenesis of RA.
类风湿性关节炎(RA)是一种常见的全身性炎症性疾病,一般认为由辅助性T1细胞驱动,不过目前的争议在于T细胞与其他白细胞的相对作用。因此,有必要更好地了解各种白细胞及其亚群在类风湿性关节炎中的作用。利用链球菌细胞壁(SCW)诱导的关节炎模型,我们使用针对谱系特异性细胞表面标志物的单克隆抗体,检测了从外周血、脾脏和淋巴结中分离出的白细胞。以CD44和CD71作为标志物评估这些细胞的激活状态。一般的T细胞,尤其是CD4 + T细胞在脾脏和淋巴结中被发现处于激活状态。脾脏中的B细胞和单核细胞也表现出激活增加。关节炎慢性期髓系和淋巴系细胞的激活表明先天性免疫和适应性免疫持续参与其中。本研究对B淋巴细胞、T淋巴细胞和髓系细胞的特定变化进行了定量分析,这与人类类风湿性关节炎的研究结果一致,在人类类风湿性关节炎中,特异性抗体、T细胞和髓系细胞均与类风湿性关节炎的发病机制有关。