Fish D C, Bare R M, Hill P R, Huebner R J
Int J Cancer. 1979 Feb;23(2):269-73. doi: 10.1002/ijc.2910230219.
C57L, NIH, and SWR mice were immunized with inactivated Gross leukemia virus (GLV) and then mated with AKR males. Their F1 offspring were then immunized with the murine sarcoma virus pseudotype of GLV, MSV(GLV). The concentrations of infectious ecotropic AKR virus in tail extracts of immunized mice were 100- to 1,000-fold lower than in non-immunized controls when tested at 30--40 days of age. Although viral titers increased slightly with time, the titers remained at least one log10 lower in the immunized mice than in non-immunized F1 control mice at all times tested. The reduction in the level of expression of endogenous ecotropic virus showed a highly significant positive correlation with the reduction in incidence of spontaneous leukemia in these mice. These data thus show that successful immunoprevention of leukemia in mice can be achieved with viral vaccines.
将C57L、NIH和SWR小鼠用灭活的格罗斯白血病病毒(GLV)进行免疫,然后与AKR雄性小鼠交配。它们的F1代后代再用GLV的鼠肉瘤病毒假型,即MSV(GLV)进行免疫。在30至40日龄时进行检测,免疫小鼠尾部提取物中感染性亲嗜性AKR病毒的浓度比未免疫的对照组低100至1000倍。尽管病毒滴度随时间略有增加,但在所有检测时间点,免疫小鼠的滴度始终比未免疫的F1对照小鼠至少低一个log10。内源性亲嗜性病毒表达水平的降低与这些小鼠自发性白血病发病率的降低呈高度显著的正相关。因此,这些数据表明,用病毒疫苗可以成功地对小鼠进行白血病的免疫预防。