Iigo M, Tsuda H, Moriyama M
Chemotherapy Division, National Cancer Center Research Institute, Tokyo, Japan.
Clin Exp Metastasis. 1994 Nov;12(6):368-74. doi: 10.1007/BF01755880.
Chemoimmunotherapy of pulmonary metastases was investigated in a protocol of combined anti-tumour agents and interferon-beta and/or interleukin-2. The combination of interferon-beta and interleukin-2 after treatment with etoposide or cisplatin exerted profound therapeutic effects in an experimental model (lung colonization) using colon carcinoma 26, which was resistant to interferon-beta or to interleukin-2 alone. Cured mice treated with anti-tumour agents and cytokines rejected re-implanted tumours. Moreover, this approach also had profound effects on spontaneous pulmonary metastases, together with the effect on primary tumours. However, this combination of cytokines did not enhance the anti-tumour activity of etoposide in athymic mice with pulmonary metastases. Injections of tumour-bearing BALB/c mice with a combination of etoposide and these cytokines resulted in a marked increase in CD8+, asialo-GM1+ cells. Thus the combined treatment with interferon-beta and interleukin-2 after administration of cytotoxic drugs may induce specific anti-tumour immunity, and such combinations may offer a new approach to the development of effective therapy for cancer metastases.
在一项联合使用抗肿瘤药物以及干扰素-β和/或白细胞介素-2的方案中,对肺转移瘤的化学免疫疗法进行了研究。在使用对单独的干扰素-β或白细胞介素-2耐药的结肠癌26构建的实验模型(肺定植)中,依托泊苷或顺铂治疗后联合使用干扰素-β和白细胞介素-2发挥了显著的治疗效果。用抗肿瘤药物和细胞因子治疗的治愈小鼠排斥重新植入的肿瘤。此外,这种方法对自发性肺转移以及对原发性肿瘤都有显著影响。然而,这种细胞因子组合在有肺转移的无胸腺小鼠中并未增强依托泊苷的抗肿瘤活性。给荷瘤BALB/c小鼠注射依托泊苷和这些细胞因子的组合导致CD8⁺、无唾液酸GM1⁺细胞显著增加。因此,在给予细胞毒性药物后联合使用干扰素-β和白细胞介素-2可能诱导特异性抗肿瘤免疫,并且这种联合可能为开发有效的癌症转移治疗方法提供新途径。