Rosenthal A, Fujinami R S, Lampert P W
Lab Invest. 1986 May;54(5):515-22.
In its natural murine host, infection with Theiler's murine encephalomyelitis virus (TMEV) produces a chronic, progressive demyelinating disease. To help elucidate the role of host immune mechanisms involved in demyelination, we studied TMEV infection in Nude mice. These animals demonstrated rising titers of infectious virus within the central nervous system and failed to produce anti-TMEV antibody. Neurologic signs including the development of severe hind limb paralysis were evident approximately 2 weeks postinfection with most animals succumbing within the first month. Immunoperoxidase studies demonstrated viral antigen in the cytoplasm of neurons and glial cells for the entire period of observation. Plaques of demyelination associated with scanty inflammatory infiltrates were present in the spinal cord by 14 days postinfection. Electron microscopic studies of the involved white matter revealed numerous degenerating glial cells, many of which contained paracrystalline arrays of picornavirus within their cytoplasm. Some of the infected glial cells were identified as oligodendrocytes by demonstrating their myelin-plasma membrane connections. The studies indicate that in Nude mice TMEV causes a lytic infection of oligodendrocytes producing demyelination independent of the T lymphocyte immune system.
在其天然的鼠类宿主中,感染泰勒氏鼠脑脊髓炎病毒(TMEV)会引发一种慢性、进行性脱髓鞘疾病。为了帮助阐明宿主免疫机制在脱髓鞘过程中的作用,我们研究了裸鼠中的TMEV感染情况。这些动物中枢神经系统内的传染性病毒滴度不断上升,且未能产生抗TMEV抗体。感染后约2周,包括严重后肢麻痹在内的神经症状明显,大多数动物在第一个月内死亡。免疫过氧化物酶研究表明,在整个观察期内,神经元和胶质细胞的细胞质中均存在病毒抗原。感染后14天,脊髓中出现了与少量炎性浸润相关的脱髓鞘斑块。对受累白质的电子显微镜研究显示,有大量退化的胶质细胞,其中许多细胞质内含有微小核糖核酸病毒的准晶体阵列。通过显示其髓磷脂-质膜连接,一些被感染的胶质细胞被鉴定为少突胶质细胞。这些研究表明,在裸鼠中,TMEV引起少突胶质细胞的溶细胞感染,导致脱髓鞘,且这一过程独立于T淋巴细胞免疫系统。