Iigo M, Nishikata K, Nakajima Y, Moriyama M
Chemotherapy Division, National Cancer Center Research Institute, Tokyo, Japan.
J Biol Regul Homeost Agents. 1989 Jul-Sep;3(3):108-11.
Treatment with a combination of recombinant human interleukin-2 (rHIL-2) and recombinant mouse interferon-beta (rIFN-beta) had a significant antitumor effect against subcutaneous (s.c.) adenocarcinoma-755 and colon-38, but this combination performed no better than rHIL-2 alone against s.c. Lewis lung carcinoma in C57BL/6 mice. Injecting a combination of rHIL-2 and rIFN-beta into mice with adenocarcinoma-755 or colon-38 tumors resulted in a marked increase in L3T4+, Lyt-2+ and asialo GM1+ cells in the peritoneal cavity. On the other hand, the treatment of mice with Lewis lung carcinoma with rHIL-2 and rIFN-beta produced almost no change of each subset in the peritoneal cavity compared to cytokine alone. Thus, sensitive tumors (adenocarcinoma-755 and colon-38) in combined treatment with rHIL-2 and rIFN-beta markedly increased L3T4+, Lyt-2+ and asialo GM1+ cells in the peritoneal cavity, but the insensitive tumor (Lewis lung carcinoma) did not.
重组人白细胞介素-2(rHIL-2)与重组小鼠干扰素-β(rIFN-β)联合治疗对皮下接种的腺癌-755和结肠癌-38具有显著的抗肿瘤作用,但在C57BL/6小鼠中,该联合治疗对皮下接种的Lewis肺癌的效果并不比单独使用rHIL-2更好。将rHIL-2和rIFN-β联合注射到患有腺癌-755或结肠癌-38肿瘤的小鼠体内,导致腹腔内L3T4+、Lyt-2+和去唾液酸GM1+细胞显著增加。另一方面,与单独使用细胞因子相比,用rHIL-2和rIFN-β治疗患有Lewis肺癌的小鼠,腹腔内各亚群几乎没有变化。因此,在联合使用rHIL-2和rIFN-β治疗时,敏感肿瘤(腺癌-755和结肠癌-38)可使腹腔内L3T4+、Lyt-2+和去唾液酸GM1+细胞显著增加,但不敏感肿瘤(Lewis肺癌)则不会。