Abe J, Wakimoto H, Aoyagi M, Hirakawa K, Hamada H
Department of Molecular Biotherapy Research, Japanese Foundation for Cancer Research, Tokyo.
Cancer Immunol Immunother. 1995 Aug;41(2):82-6. doi: 10.1007/BF01527403.
Vaccinations with tumor cells engineered to express certain cytokines have been demonstrated to induce potent and specific antitumor immunity. In our previous report, we carried out a comparative study on the ability of cytokine-gene-modified tumor vaccines to induce host immune responses, and found that irradiated tumor cells, genetically modified to secrete granulocyte/macrophage-colony-stimulating factor (GM-CSF tumor vaccine), were the most potent stimulators of systemic antitumor immunity. In this report, using the experimental tumor models in which the GM-CSF tumor vaccine was less effective in immunopotentiation, we found that the combined use of a biological response modifier (BRM) OK-432 remarkably enhanced the antitumor activity induced by the GM-CSF tumor vaccine. These data indicate the possible role of a BRM such as OK-432 to intensify further the specific tumor vaccination therapy.
用经过基因工程改造以表达某些细胞因子的肿瘤细胞进行疫苗接种,已被证明可诱导强大而特异的抗肿瘤免疫。在我们之前的报告中,我们对细胞因子基因修饰的肿瘤疫苗诱导宿主免疫反应的能力进行了比较研究,发现经基因改造以分泌粒细胞/巨噬细胞集落刺激因子的辐照肿瘤细胞(GM-CSF肿瘤疫苗)是全身抗肿瘤免疫的最有效刺激剂。在本报告中,使用GM-CSF肿瘤疫苗免疫增强效果较差的实验性肿瘤模型,我们发现生物反应调节剂(BRM)OK-432的联合使用显著增强了GM-CSF肿瘤疫苗诱导的抗肿瘤活性。这些数据表明BRM如OK-432在进一步强化特异性肿瘤疫苗治疗方面可能发挥的作用。