Hughes P J, Kirk P F, Compston D A
Section of Neurology, University of Wales College of Medicine, Heath Park, Cardiff, UK.
J Neurol Neurosurg Psychiatry. 1989 Jan;52(1):118-21. doi: 10.1136/jnnp.52.1.118.
Peripheral blood T cell phenotypes have been analysed in serial samples from patients with multiple sclerosis, their unaffected relatives and controls using a panel of antibodies chosen to distinguish T suppressor and activated suppressor cells from other CD8 lymphocytes. Overall, the percentage of Leu 2a cells correlated with alterations in the Leu 2a/15 suppressor sub-population (r = 0.79, p less than 0.001). Fewer circulating Leu 2a and Leu 2a/15 positive cells were identified in multiple sclerosis patients than unaffected individuals but there was no alteration in percentage of activated (Leu 2a/DR) CD8 cells. These findings suggest that the fluctuations in CD8 cells, characteristic of patients with multiple sclerosis, are due to alterations in T suppressor phenotype; this may then lower the threshold for activation of other T cell subpopulations.
使用一组用于区分抑制性T细胞和活化抑制性细胞与其他CD8淋巴细胞的抗体,对多发性硬化症患者、其未患病亲属和对照组的系列样本中的外周血T细胞表型进行了分析。总体而言,Leu 2a细胞的百分比与Leu 2a/15抑制性亚群的变化相关(r = 0.79,p小于0.001)。与未患病个体相比,多发性硬化症患者循环中Leu 2a和Leu 2a/15阳性细胞较少,但活化的(Leu 2a/DR)CD8细胞百分比没有变化。这些发现表明,多发性硬化症患者特有的CD8细胞波动是由于抑制性T细胞表型的改变;这可能会降低其他T细胞亚群的活化阈值。