McLeod R, Estes R G, Cohen H
Trans R Soc Trop Med Hyg. 1985;79(6):781-7. doi: 10.1016/0035-9203(85)90116-6.
Considerable evidence documents the importance of co-factors, including the immune response, in expression of oncogenicity of tumour viruses. To determine whether a common protozoal infection that can depress lymphocyte function alters manifestations of oncogenic virus infection, a mouse model of Toxoplasma infection with depressed T lymphocyte function was developed. In this model, Toxoplasma depressed blastogenic transformation to the T-cell mitogen Concanavalin A and primary antibody response to sheep red blood cells which requires T cell help. Uninfected and Toxoplasma-infected mice were then infected with Moloney leukaemia or Moloney sarcoma viruses and development of lymphoma and sarcoma were evaluated. Toxoplasma infection, which induced depression of T-cell function, decreased the incidence of Moloney sarcoma virus induced rhabdomyosarcomas but did not alter progression or regression of tumour in those mice that developed tumour. Conjoint infection with Toxoplasma and Moloney leukaemia virus did not increase incidence of lymphoma when compared with incidence of lymphoma in mice infected with Moloney leukaemia virus alone.
大量证据证明了包括免疫反应在内的辅助因子在肿瘤病毒致癌性表达中的重要性。为了确定一种能够抑制淋巴细胞功能的常见原生动物感染是否会改变致癌病毒感染的表现,构建了一种T淋巴细胞功能受抑制的弓形虫感染小鼠模型。在该模型中,弓形虫抑制了对T细胞有丝分裂原刀豆球蛋白A的母细胞转化以及对需要T细胞辅助的绵羊红细胞的初次抗体反应。然后,将未感染和感染弓形虫的小鼠感染莫洛尼白血病病毒或莫洛尼肉瘤病毒,并评估淋巴瘤和肉瘤的发生情况。诱导T细胞功能受抑制的弓形虫感染降低了莫洛尼肉瘤病毒诱导的横纹肌肉瘤的发生率,但并未改变那些发生肿瘤的小鼠中肿瘤的进展或消退情况。与仅感染莫洛尼白血病病毒的小鼠相比,弓形虫与莫洛尼白血病病毒的联合感染并未增加淋巴瘤的发生率。