Rabinovich R D, Calello M A, Boxaca M C, Quintans C J, Weissenbacher M C
Department of Microbiology, Faculty of Medicine, University of Buenos Aires, Argentina.
Intervirology. 1988;29(1):21-6. doi: 10.1159/000150025.
Splenocytes from Junin-virus-persistently-infected euthymic mice taken at 45 days postinfection seemed unable to induce overt signs of disease, to cause death, or to modify brain viral levels when transferred to athymic Junin-virus-infected mice. Findings differed sharply when the same recipients were transferred with splenocytes taken at 6 or 30 days postinfection from immunocompetent mice infected in adult life, since mortality reached 80 or 50%, respectively, and brain viral titers were significantly lowered. Furthermore, splenocytes taken at 6 days postinfection from whole adult mice proved harmless to persistently infected euthymic mice. These findings strongly suggest the existence of an immune system alteration in the immunocompetent mouse, attributable to Junin virus persistence. This premise is based on the fact that splenocytes from persistently infected mice were unable to recognize viral antigen expressed on recipient-infected cells. The absence or impairment of a specific cytotoxic T cell population is hereby postulated.
感染后45天处死的持续感染胡宁病毒的正常胸腺小鼠的脾细胞,在转移至无胸腺的感染胡宁病毒的小鼠后,似乎无法诱发明显的疾病迹象、导致死亡或改变脑内病毒水平。当相同的受体接受来自成年期感染的免疫活性小鼠在感染后6天或30天获取的脾细胞时,结果有显著差异,因为死亡率分别达到80%或50%,且脑内病毒滴度显著降低。此外,从成年小鼠整体在感染后6天获取的脾细胞对持续感染的正常胸腺小鼠无害。这些发现强烈提示,在免疫活性小鼠中存在一种归因于胡宁病毒持续感染的免疫系统改变。这一前提基于以下事实:来自持续感染小鼠的脾细胞无法识别受体感染细胞上表达的病毒抗原。据此推测存在特异性细胞毒性T细胞群体缺失或功能受损的情况。