Mathur A, Khanna N, Chaturvedi U C
Postgraduate Department of Microbiology, K.G. Medical College, Lucknow, India.
Int J Exp Pathol. 1992 Oct;73(5):603-11.
In this study we have shown, for the first time, that Japanese encephalitis virus (JEV) and a low molecular weight (10 kDa) macrophage-derived neutrophil chemotactic factor (MDF) produced following JEV infection in mice could cause an alteration in the permeability of the blood-brain barrier resulting in leakage of plasma protein bound Evans blue dye and radiolabelled erythrocytes in brain. The maximum leakage occurred at day 6 after intracerebral (i.c.) JEV infection and was sensitive to anti-JEV antisera. Further, MDF caused peak leakage of dye and radiolabelled erythrocytes at 1 h post inoculation with a decline thereafter. Complete restoration of the integrity of the blood-brain barrier occurred by the 4th hour. The extent of leakage was dose dependent and showed a direct correlation between the level of MDF, clinical sickness and virus titre in brain. Anti-MDF antisera protected the mice against the effects of MDF. These findings show that JEV-induced cytokine, MDF, alters the integrity of the blood-brain barrier and thus controls the cellular and plasma leakage into the CNS.
在本研究中,我们首次表明,日本脑炎病毒(JEV)以及小鼠感染JEV后产生的一种低分子量(10 kDa)巨噬细胞源性中性粒细胞趋化因子(MDF),可导致血脑屏障通透性改变,致使血浆中与伊文思蓝染料结合的蛋白质及放射性标记红细胞漏入脑内。脑内接种JEV后第6天出现最大程度的渗漏,且对抗JEV抗血清敏感。此外,接种MDF后1小时出现染料和放射性标记红细胞的峰值渗漏,随后渗漏量下降。血脑屏障完整性在第4小时完全恢复。渗漏程度呈剂量依赖性,且显示出MDF水平、临床疾病表现和脑内病毒滴度之间存在直接相关性。抗MDF抗血清可保护小鼠免受MDF的影响。这些发现表明,JEV诱导产生的细胞因子MDF会改变血脑屏障的完整性,从而控制细胞和血浆向中枢神经系统的渗漏。