Fallis R J, Powers M L, Weiner H L
Neurology. 1987 Apr;37(4):719-23. doi: 10.1212/wnl.37.4.719.
We have serially analyzed peripheral blood T-cell phenotypes and reactivity to myelin basic protein (MBP) during the course of acute experimental allergic encephalomyelitis (EAE) in the Lewis rat and have correlated changes with the onset of clinical disease. A reduction in total T cells (W3/13+), due primarily to a reduced helper/inducer (W3/25+) subpopulation, preceded the onset of EAE. Circulating MBP-reactive lymphocytes were only transiently present in the blood at the time EAE was clinically evident. Our findings demonstrate that in EAE, immunologic abnormalities in the peripheral blood are transient and can begin before clinical disease is evident.
我们连续分析了Lewis大鼠急性实验性变应性脑脊髓炎(EAE)病程中外周血T细胞表型及对髓鞘碱性蛋白(MBP)的反应性,并将这些变化与临床疾病的发作相关联。EAE发作前,总T细胞(W3/13+)减少,主要是由于辅助/诱导(W3/25+)亚群减少。在EAE临床症状明显时,循环中MBP反应性淋巴细胞仅短暂存在于血液中。我们的研究结果表明,在EAE中,外周血中的免疫异常是短暂的,且可在临床疾病明显之前就开始出现。