Mogensen S C, Andersen H K
Infect Immun. 1977 Aug;17(2):274-7. doi: 10.1128/iai.17.2.274-277.1977.
The role of macrophages in the difference in liver pathogenicity between herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2) in mice was investigated by selectively blocking the macrophage function of the mice by silica. Intravenous administration of 3 mg of silica 2 h before virus inoculation partially abolished the difference between the two virus types, as judged by macroscopic and microscopic examination of the livers and by virus isolation studies. Intraperitoneal inoculation of 50 mg of silical before virus seemed more effective in suppressing the macrophage function, since this treatment almost completely eliminated the difference in hepatotropism between HSV-1 and HSV-2 as assessed by the number and size of the lesions appearing in the liver. The final outcome of the infection, death from encephalitis, was, however, not influenced by macrophage blockade.
通过用二氧化硅选择性阻断小鼠的巨噬细胞功能,研究了巨噬细胞在1型单纯疱疹病毒(HSV-1)和2型单纯疱疹病毒(HSV-2)对小鼠肝脏致病性差异中的作用。在病毒接种前2小时静脉注射3毫克二氧化硅,根据肝脏的宏观和微观检查以及病毒分离研究判断,部分消除了两种病毒类型之间的差异。在病毒接种前腹腔注射50毫克二氧化硅似乎在抑制巨噬细胞功能方面更有效,因为根据肝脏中出现的病变数量和大小评估,这种处理几乎完全消除了HSV-1和HSV-2之间的嗜肝性差异。然而,感染的最终结果,即死于脑炎,不受巨噬细胞阻断的影响。