Kinjo M, Naito S, Tanaka K
Acta Pathol Jpn. 1982 May;32(3):437-43. doi: 10.1111/j.1440-1827.1982.tb01400.x.
Formation of hematogenous metastasis in the congenitally athymic nude mice (nu/nu) and their heterozygous ones (nu/+) was compared 2 weeks after an intravenous injection of xenogeneic tumor cells of rat ascites hepatoma cells (AH 130) with high thromboplastic activity. AH 130 cells formed large numbers of metastatic foci in the lungs of nu/nu recipients, while they developed into only temporary growth of metastatic foci with subsequent regression in nu/+ mice. Cellular reaction to arrested tumor cells in the pulmonary vessels was composed of large mononuclear cells, and was extensive and prominent in nu+/mice in comparison with nu/nu mice 3 days after the injection of the tumor cells. The results suggest that mononuclear cells reaction is closely related to suppression of growth of micrometastasis. This is considered as a model that highly immunogenic tumor cells attenuated and could be rejected in relation to immunological mechanisms.
在静脉注射具有高促凝活性的大鼠腹水肝癌细胞(AH 130)异种肿瘤细胞两周后,比较先天性无胸腺裸鼠(nu/nu)及其杂合子(nu/+)中血源性转移的形成情况。AH 130细胞在nu/nu受体小鼠的肺部形成大量转移灶,而在nu/+小鼠中它们仅发展为转移灶的短暂生长,随后消退。注射肿瘤细胞3天后,肺血管中停滞肿瘤细胞的细胞反应由大单核细胞组成,与nu/nu小鼠相比,nu/+小鼠中的这种反应广泛且显著。结果表明,单核细胞反应与微转移生长的抑制密切相关。这被认为是一种模型,即高免疫原性肿瘤细胞因免疫机制而减弱并可被排斥。