Wheelock E F, Caroline N L, Moore R D
J Virol. 1969 Jul;4(1):1-6. doi: 10.1128/JVI.4.1.1-6.1969.
A single inoculation of statolon into mice with established Friend virus (FV) leukemia can suppress the viral infection and produce a clinical remission lasting many months. Eventually, however, most of the mice develop characteristic FV leukemia. Persistence of FV activity in the spleens of mice during clinical remission can be demonstrated by cell transfer and histopathologic studies. Transfer to normal mice of a large number of spleen cells (10(7)) from mice in remission produces FV leukemia, and transfer of a small number of cells (10(2)) produces immunity to FV challenge. Histopathologic examination reveals clusters of abnormal FV leukemia-like cells directly beneath the capsules of the spleens of mice in clinical remission.
将链格孢菌素单次接种到患有已确立的弗氏病毒(FV)白血病的小鼠体内,可抑制病毒感染并产生持续数月的临床缓解。然而,最终大多数小鼠会发展出典型的FV白血病。通过细胞转移和组织病理学研究可以证明,在临床缓解期间小鼠脾脏中FV活性的持续存在。将处于缓解期的小鼠的大量脾细胞(10⁷)转移到正常小鼠体内会引发FV白血病,而转移少量细胞(10²)则会产生对FV攻击的免疫力。组织病理学检查显示,在临床缓解期的小鼠脾脏被膜下方有异常的FV白血病样细胞簇。