Horneff G, Hanson M, Wahn V
Department of Pediatrics, University of Düsseldorf, Germany.
Rheumatol Int. 1993;12(6):221-6. doi: 10.1007/BF00301005.
The V beta chain repertoire in peripheral blood T-cell was analyzed in 23 patients with juvenile rheumatoid arthritis (JRA). Of these, 15 patients had active disease as defined by tender and swollen joints. The ESR was elevated in all but three patients, C-reactive protein (CRP) was elevated in eight. Three patients were investigated during active and inactive phases of the disease. In the active phase of the disease T-cell composition was characterized by an increased number of CD4+ helper cells due to a marked increase in the CD4+CD45RA+ subgroup (34.0 +/- 10.9%, P < 0.001) and a decrease in CD8+CD29+ T-cells (10.3 +/- 5.6%, P < 0.05) compared to controls (15.4 +/- 10.0% and 17.8 +/- 12.3%, respectively). Using the monoclonal antibodies available to determine T-cell receptor (TCR) expression, patients with active disease demonstrated a significant predominance of T-cells bearing TCRs of the V beta 5 family as determined by flow cytometry (7.6 +/- 6.7 vs 3.4 +/- 1.3 in controls, P = 0.01). In active polyarthritis, up to 24% of peripheral blood T-cells expressed TCRs of the same family. In the majority of JRA patients and especially in non-active disease, no preferential TCRs were found compared to controls. However, even defining only a part of TCRs by immunofluorescence, in certain patients a preferential or dominant expression of a single V beta gene family in the T-cells was found, supporting the concept of an involvement of T-cells in the autoimmune pathogenesis of JRA.
对23例青少年类风湿性关节炎(JRA)患者外周血T细胞中的Vβ链谱进行了分析。其中,15例患者患有活动性疾病,根据关节压痛和肿胀来定义。除3例患者外,所有患者的血沉均升高,8例患者的C反应蛋白(CRP)升高。对3例患者在疾病的活动期和非活动期进行了研究。在疾病的活动期,T细胞组成的特征是CD4+辅助性T细胞数量增加,这是由于CD4+CD45RA+亚组显著增加(34.0±10.9%,P<0.001),与对照组相比,CD8+CD29+T细胞减少(10.3±5.6%,P<0.05)(对照组分别为15.4±10.0%和17.8±12.3%)。使用可获得的单克隆抗体来测定T细胞受体(TCR)表达,通过流式细胞术测定,患有活动性疾病的患者中携带Vβ5家族TCR的T细胞显著占优势(7.6±6.7 vs对照组的3.4±1.3,P=0.01)。在活动性多关节炎中,高达24%的外周血T细胞表达同一家族的TCR。在大多数JRA患者中,尤其是在非活动性疾病患者中,与对照组相比未发现优先的TCR。然而,即使仅通过免疫荧光确定部分TCR,在某些患者中也发现T细胞中单个Vβ基因家族存在优先或显性表达,这支持了T细胞参与JRA自身免疫发病机制的概念。