Wang F I, Stohlman S A, Fleming J O
Department of Neurology, School of Medicine, University of Southern California, Los Angeles 90033.
J Neuroimmunol. 1990 Nov;30(1):31-41. doi: 10.1016/0165-5728(90)90050-w.
The neurotropic mouse hepatitis viruses (MHV), in particular strain JHM (JHMV or MHV-4), cause experimental central nervous system demyelination that pathologically resembles multiple sclerosis, an important human demyelinating disease. The mechanism of JHMV-induced demyelination remains unclear, though its tropism for oligodendrocytes had led to the belief that JHMV causes demyelination by direct lysis of these myelin-producing cells. However, several studies have also implicated the involvement of immune responses in the demyelinating process. In this communication, we present evidence that generalized immunosuppression with gamma irradiation prevents JHMV-induced demyelination, a finding that was not limited to a particular strain of JHMV or to one strain of mouse. In addition, significant paralytic-demyelinating disease was restored to infected, irradiated mice after the adoptive transfer of nylon wool nonadherent splenic cells and appeared to be restricted by the major histocompatibility complex (MHC). These observations indicate that the principal mechanisms of JHMV-induced demyelination are most likely immunopathological.
嗜神经性小鼠肝炎病毒(MHV),特别是JHM株(JHMV或MHV - 4),可引起实验性中枢神经系统脱髓鞘,其病理表现类似于多发性硬化症,这是一种重要的人类脱髓鞘疾病。尽管JHMV对少突胶质细胞具有嗜性,导致人们认为JHMV通过直接裂解这些产生髓磷脂的细胞而引起脱髓鞘,但JHMV诱导脱髓鞘的机制仍不清楚。然而,多项研究也表明免疫反应参与了脱髓鞘过程。在本通讯中,我们提供证据表明,γ射线全身免疫抑制可预防JHMV诱导的脱髓鞘,这一发现不限于特定的JHMV株或某一品系的小鼠。此外,在过继转移尼龙毛非黏附脾细胞后,感染并接受照射的小鼠恢复了严重的麻痹性脱髓鞘疾病,且似乎受主要组织相容性复合体(MHC)限制。这些观察结果表明,JHMV诱导脱髓鞘的主要机制很可能是免疫病理学机制。