Melendro E I, Saldate C, Rivero S J, Alarcon-Segovia D
Clin Immunol Immunopathol. 1983 Jun;27(3):340-7. doi: 10.1016/0090-1229(83)90086-7.
We studied by flow cytometry using monoclonal antibodies the T3, T4, and T8 subpopulations of T cells in the peripheral blood of 109 patients with various connective tissue diseases who were not receiving any treatment. Comparison of the results was made with those obtained with normal controls matched for age and sex with each connective tissue disease group. When compared as disease groups, patients with systemic lupus erythematosus (n = 41) had decreased T8 cells, but patients with active disease (n = 17) had all three T-cell subpopulations lower than their controls, whereas those with inactive disease (n = 24) showed no differences. Patients with rheumatoid arthritis (n = 23) had decreased T3 and T8 cells, whereas patients with scleroderma (n = 22) only had decreased T3 cells, and patients with primary Sjögren's syndrome (n = 15) had lower proportions of all three T-cell subpopulations than their matched controls. Patients with mixed connective tissue disease (n = 8) had proportions of all three T-cell subpopulations akin to those of their matched controls, but showed a tendency to have decreased T8 cells that reached statistical significance when compared to the entire control group. Although our findings tend to support the notion that the abnormalities in immunoregulatory T-cell circuits leading to autoimmunity are different in each connective tissue disease, the great variability found in both patients and controls seems to preclude the use of these determinations in individual patients for clinical purposes.
我们使用单克隆抗体通过流式细胞术研究了109例未接受任何治疗的各种结缔组织疾病患者外周血中T细胞的T3、T4和T8亚群。将结果与各结缔组织疾病组年龄和性别匹配的正常对照者的结果进行比较。作为疾病组进行比较时,系统性红斑狼疮患者(n = 41)的T8细胞减少,但活动期疾病患者(n = 17)的所有三个T细胞亚群均低于其对照者,而疾病非活动期患者(n = 24)则无差异。类风湿关节炎患者(n = 23)的T3和T8细胞减少,而硬皮病患者(n = 22)仅T3细胞减少,原发性干燥综合征患者(n = 15)的所有三个T细胞亚群比例均低于其匹配的对照者。混合性结缔组织病患者(n = 8)的所有三个T细胞亚群比例与匹配的对照者相似,但与整个对照组相比,其T8细胞有减少的趋势,且达到统计学意义。尽管我们的研究结果倾向于支持这样一种观点,即导致自身免疫的免疫调节性T细胞回路异常在每种结缔组织疾病中都不同,但在患者和对照者中发现的巨大变异性似乎排除了将这些测定用于个体患者临床目的的可能性。