Miller D J, Rivera-Quiñones C, Njenga M K, Leibowitz J, Rodriguez M
Department of Immunology, Mayo Clinic and Foundation, Rochester, Minnesota 55905, USA.
J Neurosci. 1995 Dec;15(12):8345-52. doi: 10.1523/JNEUROSCI.15-12-08345.1995.
Animal models with selective genetic immunodeficiencies are useful tools to identify pathogenic mechanisms of disease. Resistant (C57BL/6F 129/J) (H-2b) mice are rendered susceptible to Theiler's murine encephalomyelitis virus-induced demyelination by genetic disruption of the beta 2 microglobulin gene [beta 2 m(-l-)]. The absence of beta 2 m prevents the expression of major histocompatibility complex class I molecules and normal levels of functional CD8+ T cells. We tested whether genetic depletion of beta 2 m would permit CNS remyelination after chronic demyelination induced by the Daniel's strain of Theiler's virus. In contrast to the minimal spontaneous remyelination observed in SJL/J mice after infection with the Daniel's strain of Theiler's virus, chronically infected beta 2 m(-I-) mice showed extensive and progressive spontaneous CNS remyelination at 6, 12, and 18 months after infection. Spontaneous remyelination by both oligodendrocytes and Schwann cells occurred despite the presence of persistent virus antigen and RNA, but was associated with diminished virus-specific humoral and delayed-type hypersensitivity responses. These experiments support the hypothesis that the immune response inhibits myelin regeneration after virus-induced CNS demyelination.
具有选择性遗传免疫缺陷的动物模型是识别疾病致病机制的有用工具。通过β2微球蛋白基因(β2m(-/-))的基因破坏,抗性(C57BL/6F 129/J)(H-2b)小鼠对泰勒氏鼠脑脊髓炎病毒诱导的脱髓鞘变得易感。β2m的缺失阻止了主要组织相容性复合体I类分子的表达以及功能性CD8+T细胞的正常水平。我们测试了β2m的基因缺失是否会在泰勒氏病毒丹尼尔株诱导的慢性脱髓鞘后允许中枢神经系统重新髓鞘化。与感染泰勒氏病毒丹尼尔株的SJL/J小鼠中观察到的最小程度的自发重新髓鞘化相反,慢性感染的β2m(-/-)小鼠在感染后6、12和18个月显示出广泛且进行性的中枢神经系统自发重新髓鞘化。尽管存在持续的病毒抗原和RNA,但少突胶质细胞和雪旺细胞均发生了自发重新髓鞘化,不过这与病毒特异性体液反应和迟发型超敏反应减弱有关。这些实验支持了免疫反应抑制病毒诱导的中枢神经系统脱髓鞘后髓鞘再生的假说。