Bishop S A, Hill T J
Department of Microbiology, University of Bristol, U.K.
J Neurol Sci. 1989 Jun;91(1-2):109-18. doi: 10.1016/0022-510x(89)90080-4.
Two models of herpes simplex virus (HSV) infection in the mouse (inoculation of the ear pinna or intravenous inoculation) were used to assess immune responses to the virus and myelin basic protein (MBP). In both models demyelination in the central nervous system (CNS) can be assessed by clinical signs; ear paralysis (ear inoculation) and hind limb paralysis (intravenous inoculation). In the ear model, low levels of antibody to MBP were detected at 7 and 14 days after inoculation. The incidence of such antibody was low and bore no correlation with signs of paralysis. Cells from draining lymph nodes of mice inoculated in the pinna showed a proliferative response to HSV and MBP in vitro. In both models, delayed-type hypersensitivity reactions were demonstrated against HSV and MBP but such reactions were most significant after i.v. inoculation. This may reflect the greater CNS damage associated with hind limb paralysis.
采用两种小鼠单纯疱疹病毒(HSV)感染模型(耳廓接种或静脉接种)来评估对该病毒和髓鞘碱性蛋白(MBP)的免疫反应。在这两种模型中,中枢神经系统(CNS)的脱髓鞘可通过临床体征来评估;耳部麻痹(耳部接种)和后肢麻痹(静脉接种)。在耳部模型中,接种后7天和14天检测到低水平的抗MBP抗体。此类抗体的发生率较低,且与麻痹体征无关。接种于耳廓的小鼠引流淋巴结中的细胞在体外对HSV和MBP表现出增殖反应。在这两种模型中,均证实对HSV和MBP存在迟发型超敏反应,但此类反应在静脉接种后最为显著。这可能反映了与后肢麻痹相关的更严重的中枢神经系统损伤。