Sharpin R K, Wilson J D
Clin Exp Immunol. 1977 Aug;29(2):205-12.
A modified method for estimating erythrocyte-antibody (EA) rosette formation of human peripheral blood lymphocytes (PBL) reveals consistent differences between rheumatoid arthritis (RA) patients tested and healthy control subjects. Using this method we find an average of 27 +/- 0-8% (standard error of mean) of PBL from 120 RA patients forming EA rosettes in contrast to only 6 +/- 0-6% of PBL from ninety-five healthy controls, and 7 +/- 0-9% from eighteen patients with systemic lupus erythematosus (SLE). This difference is not due to monocytes forming EA rosettes or to T-cell sheep red blood cell (SRBC) binding. The concentration of antibody used in our assay appears to highlight the RA-control differences--suggesting a possible qualitative difference in EA-binding capacity. We find no correlation between EA binding and disease duration or rheumatoid factor titre. The assay is susceptible to technical variation, and the effects of antibody concentration, lymphocyte to SRBC ratio, method of blood collection and lymphocyte-separation procedure have all been evaluated.
一种用于估计人外周血淋巴细胞(PBL)红细胞抗体(EA)花环形成的改良方法显示,在接受检测的类风湿性关节炎(RA)患者与健康对照受试者之间存在一致的差异。使用该方法,我们发现120例RA患者的PBL平均有27±0.8%(均值标准误)形成EA花环,相比之下,95例健康对照的PBL只有6±0.6%形成EA花环,18例系统性红斑狼疮(SLE)患者的PBL为7±0.9%。这种差异并非由于单核细胞形成EA花环或T细胞与绵羊红细胞(SRBC)结合所致。我们检测中使用的抗体浓度似乎突出了RA患者与对照之间的差异,这表明EA结合能力可能存在质的差异。我们发现EA结合与疾病持续时间或类风湿因子滴度之间没有相关性。该检测易受技术变异影响,我们已评估了抗体浓度、淋巴细胞与SRBC比例、采血方法和淋巴细胞分离程序的影响。