Boche D, Gray F, Chakrabarti L, Hurtrel M, Montagnier L, Hurtrel B
Unité d'Oncologie Virale, Institut Pasteur, Paris.
Neuropathol Appl Neurobiol. 1995 Dec;21(6):535-9. doi: 10.1111/j.1365-2990.1995.tb01100.x.
To assess the susceptibility of resident microglia to simian immunodeficiency virus (SIV) infection, we analysed the brains of rhesus macaques after intracerebral (i.c.) inoculation of the virus into the central region at 7 days, 1, 2 and 3 months post-inoculation (p.i.). The brains of animals showed the same moderate neuropathological changes in central, frontal and parietal regions of the brain, characterized by gliosis, microglial nodules, perivascular infiltrates and occasional white matter pallor and similar low numbers of infected cells detected by in situ hybridization. These results, showing that i.c. inoculation did not lead to preferential infection of brain tissue, even near the inoculation point at 7 days p.i., provide evidence for the low susceptibility of resident microglia to SIV replication during the early stages of infection.
为评估常驻小胶质细胞对猴免疫缺陷病毒(SIV)感染的易感性,我们分析了恒河猴在接种病毒后7天、1个月、2个月和3个月时,经脑内(i.c.)将病毒接种到脑中央区域后的脑部情况。动物的大脑在脑中央、额叶和顶叶区域呈现相同程度的中度神经病理学变化,其特征为胶质增生、小胶质细胞结节、血管周围浸润以及偶尔出现的白质苍白,并且通过原位杂交检测到的感染细胞数量相似且较少。这些结果表明,即使在接种后7天靠近接种点处,脑内接种也不会导致脑组织的优先感染,这为常驻小胶质细胞在感染早期对SIV复制的低易感性提供了证据。