Shimojima Y, Matsuda M, Ishii W, Gono T, Ikeda S
Department of Internal Medicine (Neurology and Rheumatology), Shinshu University School of Medicine, Matsumoto, Japan.
Clin Exp Rheumatol. 2008 Nov-Dec;26(6):1079-82.
Clinical pictures of poly-myalgia rheumatica (PMR) and remitting seronegative symmetrical synovitis with pitting edema (RS3PE) are often indistinguishable from those of early rheumatoid arthritis (RA). To investigate whether there is a difference in immunological aspects among these 3 disorders, we performed a phenotypic analysis of peripheral blood lymphocytes.
Eleven patients with early RA, 14 with PMR and 11 with RS3PE were enrolled in this study. After separation of mononuclear cells from peripheral blood using the Ficoll-Hypaque method, surface markers and intracellular cytokines of lymphocytes were analyzed by 2- or 3-color flow cytometry.
Both PMR and RS3PE showed a significant decrease in CD8CD25 cells (p<0.05), and significant increases in CD4IFN-gammaIL-4- (p<0.05), CD8IFN-gammaIL-4- (p<0.05 and p<0.01, respectively) and CD4TNF-alpha cells (p<0.05) compared with early RA. CD3CD4 cells were higher in PMR than in RS3PE (p<0.01), but there were no significant differences in any other phenotypes between these disorders.
A decrease in activated cytotoxic/suppressor T cells and increases in circulating Th1 and Tc1 cells may be common characteristics of PMR and RS3PE in comparison with early RA. Both disorders are clearly different from early RA, and probably belong to the same disease entity with regard to phenotypes of peripheral blood lymphocytes.
风湿性多肌痛(PMR)和缓解性血清阴性对称性滑膜炎伴凹陷性水肿(RS3PE)的临床表现常与早期类风湿关节炎(RA)难以区分。为研究这三种疾病在免疫学方面是否存在差异,我们对外周血淋巴细胞进行了表型分析。
本研究纳入了11例早期RA患者、14例PMR患者和11例RS3PE患者。采用Ficoll-Hypaque法从外周血中分离单个核细胞后,通过双色或三色流式细胞术分析淋巴细胞的表面标志物和细胞内细胞因子。
与早期RA相比,PMR和RS3PE的CD8CD25细胞均显著减少(p<0.05),而CD4IFN-γIL-4-(p<0.05)、CD8IFN-γIL-4-(分别为p<0.05和p<0.01)以及CD4TNF-α细胞显著增加(p<0.05)。PMR中的CD3CD4细胞高于RS3PE(p<0.01),但这两种疾病在其他任何表型上均无显著差异。
与早期RA相比,活化的细胞毒性/抑制性T细胞减少以及循环中的Th1和Tc1细胞增加可能是PMR和RS3PE的共同特征。这两种疾病均与早期RA明显不同,在外周血淋巴细胞表型方面可能属于同一疾病实体。