Studies on activation variables in multiple sclerosis.

S Fredrikson
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Abstract

The study aimed to evaluate the usefulness of some selected immune variables as markers of disease activation, progression and possible etiopathogenesis of multiple sclerosis (MS). Levels of neopterin, a factor known to be released from macrophages and monocytes at increased rates in cellular immune reactions were higher in cerebrospinal fluid (CSF) from patients with MS during exacerbations in comparison with remissions. The elevation in CSF during exacerbations was not reflected in serum. Expression of HLA class II antigens (DR) on activated T lymphocytes in CSF were encountered at elevated percentage in only 10% of patients with MS, against 81% of patients with acute aseptic meningoencephalitis (AM). In patients with AM, the DR expression on CSF T cells was found on both CD8+ and CD4+ cells. There was no correlation between percentage of DR+ T cells in CSF and disability, exacerbation/remission or recent onset of disease in patients with MS. Phenotypic characterization of mononuclear cells in CSF and peripheral blood revealed increased proportion of CD5+ cells in CSF compared to peripheral blood which in MS was not reflected by any changes in CD4+ or CD8+ cells, while in AM the increase of CD5+ cells in CSF was followed by increase of CD4+ cells. A population of CD5+, CD8-, CD4- cells might be postulated to occur in MS CSF. Levels of CD8+ cells in peripheral blood and CSF did not fluctuate in parallel with disease activity as measured as clinical exacerbation. OKB7+, OKM1+ and HLA-DR+ cells differed significantly between CSF and peripheral blood, indicative of a selective passage of cells into the central nervous system (CNS) - CSF compartment. Proliferating cells expressing transferrin receptors (OKT9) were generally few or absent in CSF of patients with MS. MS patients' bone marrow mononuclear cells showed higher spontaneous proliferation both in comparison with cells from bone marrow of control subjects and peripheral blood lymphocytes from MS patients. PHA response of bone marrow mononuclear cells from MS patients was also higher than that from controls. There was, however, no significant difference in proliferative response of peripheral blood lymphocytes between MS patients and controls. Seven of 11 MS patients showed morphological signs of activation in their bone marrow, without correlation to patients' clinical condition. Higher levels of undifferentiated or activated cells, measured as OKT10+ cells were found in peripheral blood of patients with MS compared to controls.(ABSTRACT TRUNCATED AT 400 WORDS)

多发性硬化症激活变量研究。
该研究旨在评估一些选定的免疫变量作为多发性硬化症(MS)疾病激活、进展和可能的发病机制标志物的有用性。多发性硬化症患者脑脊液(CSF)中的蝶呤(一种已知在细胞免疫反应中会从巨噬细胞和单核细胞中以更高的速度释放的因子)水平与缓解期相比更高。加重期脑脊液中的升高在血清中没有反映。CSF 中活化 T 淋巴细胞上的 HLA 二类抗原(DR)表达升高的比例在多发性硬化症患者中仅占 10%,而在急性无菌性脑膜脑炎(AM)患者中则占 81%。在急性无菌性脑膜脑炎患者中,CD8+和CD4+细胞的CSF T细胞上都有DR表达。多发性硬化症患者脑脊液中DR+ T细胞的百分比与残疾、病情加重/缓解或近期发病之间没有相关性。脑脊液和外周血中单核细胞的表型特征显示,与外周血相比,脑脊液中 CD5+ 细胞的比例增加了。可以推测在多发性硬化症患者的 CSF 中会出现 CD5+、CD8-、CD4- 细胞群。外周血和 CSF 中 CD8+ 细胞的水平并不随疾病活动(以临床恶化程度衡量)而波动。CSF和外周血中的OKB7+、OKM1+和HLA-DR+细胞差异显著,表明细胞有选择性地进入中枢神经系统(CNS)-CSF区。在多发性硬化症患者的脑脊液中,表达转铁蛋白受体(OKT9)的增殖细胞通常很少或没有。与对照组骨髓细胞和多发性硬化症患者外周血淋巴细胞相比,多发性硬化症患者的骨髓单核细胞显示出更高的自发性增殖。多发性硬化症患者骨髓单核细胞的 PHA 反应也高于对照组。然而,多发性硬化症患者与对照组的外周血淋巴细胞增殖反应无明显差异。11 名多发性硬化症患者中有 7 人的骨髓出现了活化的形态学迹象,但与患者的临床状况无关。与对照组相比,多发性硬化症患者外周血中以 OKT10+ 细胞衡量的未分化或活化细胞水平更高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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