Mazurenko N P, Iakovleva L S, Shcherbak N P, Pavlovskaia A I, Zueva Iu N
Eksp Onkol. 1987;9(1):41-6.
Mouse vaccination with alive endogenous N-tropic virus OA-3 inhibited and decreased the development of the Rauscher leukemia in C57B1/6 mice (B-type) and SWR mice (N-type) as well as the development 7,12-dimethyl benzanthracene (DMBA)-induced tumours in mouse hybrids (neither N-, nor B-types). The effect of vaccination was DMBA- or MLV-P-dose-dependent. Vaccination with the same virus did not affect the incidence of gamma-irradiation-induced leukemia in CBA mice (N-type) and C57B1/6 mice while it increased twice the incidence of radiation leukemia in DBA mice (N-type). However, the incidence of thymomas lowered in radiation leukemia-bearing vaccinated mice of all the 3 strains, which may result from inhibition of murine thymotropic endogenous virus reproduction. The data obtained indicate the participation of murine own endogenous viruses in DMBA- or gamma-irradiation induced carcinogenesis.
用活的内源性N向性病毒OA - 3对小鼠进行免疫接种,可抑制并减少C57B1/6小鼠(B型)和SWR小鼠(N型)中劳斯氏白血病的发展,以及小鼠杂种(既非N型也非B型)中7,12 - 二甲基苯并蒽(DMBA)诱导肿瘤的发展。疫苗接种的效果呈DMBA或MLV - P剂量依赖性。用相同病毒进行免疫接种对CBA小鼠(N型)和C57B1/6小鼠中γ射线诱导的白血病发病率没有影响,而在DBA小鼠(N型)中,它使辐射性白血病的发病率增加了两倍。然而,在所有这3个品系中,接种疫苗的患辐射性白血病小鼠的胸腺瘤发病率降低了,这可能是由于抑制了嗜鼠胸腺内源性病毒的繁殖。所获得的数据表明,小鼠自身的内源性病毒参与了DMBA或γ射线诱导的致癌过程。