Robertson M N, Spangrude G J, Hasenkrug K, Perry L, Nishio J, Wehrly K, Chesebro B
Laboratory of Persistent Viral Diseases, National Institute of Allergy and Infectious Diseases, Hamilton, Montana 59840.
J Virol. 1992 Jun;66(6):3271-7. doi: 10.1128/JVI.66.6.3271-3277.1992.
Spontaneous recovery from Friend virus complex-induced leukemic splenomegaly in H-2Db/b mice correlated with the appearance of Friend virus complex-specific cytotoxic T lymphocytes (CTL) detectable directly in spleen cell populations. By testing CTL on target cells containing expression vectors encoding individual retroviral structural proteins, the main viral protein recognized was shown to be the Friend murine leukemia helper virus envelope glycoprotein. In vivo depletion of CD8-positive T cells drastically reduced the incidence of recovery, providing direct evidence for the role of CD8-positive CTL in the spontaneous recovery process. In vivo depletion of CD4-positive cells had little effect on the early stages of recovery but did cause a marked reduction in the final incidence of recovery at 60 to 90 days. Thus, CD8-positive cells were required for the initiation of the recovery process, whereas CD4-positive cells appeared to be required for maintenance of the recovered status.
在H-2Db/b小鼠中,从Friend病毒复合物诱导的白血病性脾肿大中自发恢复与在脾细胞群体中可直接检测到的Friend病毒复合物特异性细胞毒性T淋巴细胞(CTL)的出现相关。通过在含有编码单个逆转录病毒结构蛋白的表达载体的靶细胞上测试CTL,结果表明被识别的主要病毒蛋白是Friend鼠白血病辅助病毒包膜糖蛋白。体内清除CD8阳性T细胞可大幅降低恢复的发生率,这为CD8阳性CTL在自发恢复过程中的作用提供了直接证据。体内清除CD4阳性细胞对恢复的早期阶段影响不大,但确实导致60至90天时最终恢复发生率显著降低。因此,恢复过程的启动需要CD8阳性细胞,而维持恢复状态似乎需要CD4阳性细胞。