Reder A T, Antel J P, Oger J J, McFarland T A, Rosenkoetter M, Arnason B G
Ann Neurol. 1984 Aug;16(2):242-9. doi: 10.1002/ana.410160214.
The median fluorescence intensity of peripheral blood T8+ (T-suppressor/cytotoxic) cells in patients with active (relapsing or progressive) or stable multiple sclerosis (MS) and in control subjects was determined with a fluorescence-activated cell sorter using an indirect immunofluorescence assay. Median fluorescence intensity was significantly lower in patients with active MS than in controls. No differences in median fluorescence intensity were found between patients with stable MS and controls. Analysis of T8+ cells that had been modulated in vitro with OKT8 indicated that the resultant reduction in the median T8 antigen density per cell resulted in fewer T8+ cells being enumerated when the fluorescence-activated cell sorter was used than when a fluorescence microscope was used. Reduced median T8 antigen density on cells as found in active MS may contribute to the apparent underrepresentation of circulating T-suppressor cells in such patients and may be associated with reduced suppressor cell function.
采用间接免疫荧光测定法,通过荧光激活细胞分选仪测定了活动期(复发型或进展型)或稳定型多发性硬化症(MS)患者及对照受试者外周血T8 +(T抑制/细胞毒性)细胞的中位荧光强度。活动期MS患者的中位荧光强度显著低于对照组。稳定型MS患者与对照组之间的中位荧光强度未发现差异。对用OKT8体外调节的T8 +细胞的分析表明,每个细胞中T8抗原密度的中位数降低,导致使用荧光激活细胞分选仪时计数的T8 +细胞比使用荧光显微镜时少。在活动期MS患者中发现的细胞上T8抗原密度中位数降低,可能导致此类患者循环T抑制细胞明显减少,并可能与抑制细胞功能降低有关。