Tsukada N, Matsuda M, Miyagi K, Yanagisawa N
Department of Neurology, Shinshu University School of Medicine, Matsumoto, Japan.
Autoimmunity. 1993;14(4):329-33. doi: 10.3109/08916939309079236.
To investigate the factors regulating the entry of lymphocytes into the brain, we assessed the adhesion in vitro of 51Cr labelled lymphocytes from peripheral blood of patients with multiple sclerosis (MS) to human cerebral endothelial cells, and evaluated the effect on the adhesion of endothelium activated by interferon-gamma (IFN-gamma), lipopolysaccharides (LPS), interleukin-1 (IL-1) and tumor necrosis factor (TNF). Patients with acute relapsing MS during an exacerbation showed significant increase in MNC adherence to cerebral endothelial cells as compared with controls (p < 0.001). MNC adherence to cerebral endothelial cells activated by IFN-gamma or LPS, was significantly increased as compared to the controls (p < 0.01). MNC adherence to endothelial cells was not blocked by antibodies against the intercellular adhesion molecule-1 (ICAM-1), but was blocked by lymphocyte function-associated antigen-1 (LFA-1). The increased adherence observed in patients with acute relapsing MS during an exacerbation would modulate the migration of lymphocytes across the blood-brain barrier (BBB).
为研究调节淋巴细胞进入脑内的因素,我们评估了来自多发性硬化症(MS)患者外周血的51Cr标记淋巴细胞与人类脑内皮细胞的体外黏附情况,并评估了干扰素-γ(IFN-γ)、脂多糖(LPS)、白细胞介素-1(IL-1)和肿瘤坏死因子(TNF)激活内皮细胞对黏附的影响。与对照组相比,处于病情加重期的急性复发型MS患者的单核细胞(MNC)对脑内皮细胞的黏附显著增加(p < 0.001)。与对照组相比,IFN-γ或LPS激活的脑内皮细胞对MNC的黏附显著增加(p < 0.01)。抗细胞间黏附分子-1(ICAM-1)抗体不能阻断MNC与内皮细胞的黏附,但淋巴细胞功能相关抗原-1(LFA-1)抗体可阻断该黏附。处于病情加重期的急性复发型MS患者中观察到的黏附增加会调节淋巴细胞穿过血脑屏障(BBB)的迁移。