Salvarani C, Boiardi L, Macchioni P, Casadei Maldini M, Mancini R, Beltrandi E, Rossi F, Portioli I
2nd Divisione di Medicina (Unità Reumatologica), Arcispedale S. Maria Nuova, Reggio Emilia, Italy.
J Rheumatol. 1994 Oct;21(10):1865-9.
Soluble CD4 (sCD4) and sCD8 were measured in the sera of 19 patients with active polymyalgia rheumatica (PMR).
We correlated the results obtained with lymphocyte subpopulations, soluble interleukin 2 receptors (sIL-2R), and clinical and laboratory variables at diagnosis. In addition 15 patients were prospectively studied during a 6 month period of prednisone therapy. Assays of the sCD4 and sCD8 molecules and of the sIL-2R were performed using an enzyme-linked immunosorbent kit.
Serum sCD8 and sIL-2R levels were significantly elevated in patients with active disease compared to normal controls, while serum sCD4 and the relative percentage of CD8+ T cell levels decreased. In the 15 patients prospectively studied sCD8 levels fell significantly after 1 week of therapy along with the remission of clinical disease and normalization of erythrocyte sedimentation rate. At the end of the study period, sCD8 values did not differ from normal controls and they were significantly reduced compared to baseline values. CD8+ lymphopenia persisted at the end of the study. sCD4 levels remained significantly lower during the study period. sIL-2R levels fell significantly at the end of the study period. However, the 6-month levels of sIL-2R remained significantly higher compared to controls.
The rise of serum sCD8 levels observed in patients with PMR with active disease suggests an early activation of CD8 T cells. The therapeutic effect of steroid in PMR may be partially mediated by its effect on CD8 activated cells.
检测19例活动期风湿性多肌痛(PMR)患者血清中的可溶性CD4(sCD4)和sCD8水平。
将所得结果与诊断时的淋巴细胞亚群、可溶性白细胞介素2受体(sIL-2R)以及临床和实验室指标进行关联分析。此外,对15例患者进行了为期6个月的泼尼松治疗前瞻性研究。使用酶联免疫吸附试剂盒检测sCD4和sCD8分子以及sIL-2R。
与正常对照组相比,活动期疾病患者的血清sCD8和sIL-2R水平显著升高,而血清sCD4和CD8 + T细胞水平的相对百分比降低。在15例前瞻性研究的患者中,治疗1周后sCD8水平随临床疾病缓解和红细胞沉降率正常化而显著下降。在研究期结束时,sCD8值与正常对照组无差异,且与基线值相比显著降低。研究结束时CD8 +淋巴细胞减少持续存在。研究期间sCD4水平仍显著较低。研究期结束时sIL-2R水平显著下降。然而,sIL-2R的6个月水平仍显著高于对照组。
在活动期PMR患者中观察到的血清sCD8水平升高表明CD8 T细胞早期激活。类固醇在PMR中的治疗作用可能部分由其对CD8激活细胞的作用介导。