Price M R, Baldwin R W
Br J Cancer. 1974 Nov;30(5):394-400. doi: 10.1038/bjc.1974.213.
Subcellular fractions from an aminoazo dye induced rat hepatoma (D23) were examined for their ability to evoke rejection responses in syngeneic hosts to transplanted tumour cells and to induce the production of humoral antibody. Membrane fractions isolated by zonal centrifugation and displaying an increased activity of tumour specific antigen (Price and Baldwin, 1974), as well as crude membrane fractions and purified tumour cell ghosts, all elicited tumour specific antibody demonstrable by membrane immunofluorescence staining of viable hepatoma D23 cells. Tumour cell nuclei or soluble cytoplasmic protein were, however, lacking in this capacity. Resistance to tumour cell challenge was not observed in rats treated with any of the hepatoma D23 subcellular fractions administered by various routes either alone or in admixture with bacterial adjuvants. These findings are relevant to current views that tumour immunity may be more optimally achieved by inoculation of intact (viable or attenuated) tumour cells.
检测了氨基偶氮染料诱导的大鼠肝癌(D23)的亚细胞组分,观察其在同基因宿主体内引发对移植肿瘤细胞的排斥反应以及诱导体液抗体产生的能力。通过区带离心分离得到的膜组分,其肿瘤特异性抗原活性增强(普赖斯和鲍德温,1974年),还有粗制膜组分和纯化的肿瘤细胞空壳,均可通过对活的肝癌D23细胞进行膜免疫荧光染色检测到肿瘤特异性抗体。然而,肿瘤细胞核或可溶性细胞质蛋白却没有这种能力。单独或以与细菌佐剂混合的方式通过各种途径给予肝癌D23亚细胞组分处理的大鼠,未观察到对肿瘤细胞攻击的抗性。这些发现与当前观点相关,即通过接种完整(活的或减毒的)肿瘤细胞可能能更有效地实现肿瘤免疫。