Zaloom Y, Gallagher G
University of Glasgow Department of Surgery, Glasgow Royal Infirmary, Scotland, U.K.
Anticancer Res. 1993 Jul-Aug;13(4):1081-5.
We have examined the relative abilities of interleukin-4 (IL-4) and interleukin-2 (IL-2) to inhibit the growth of the B.16 melanoma in C57BL/6 mice. Tumours were allowed to become established and then treated peritumourally with either IL-4 or IL-2, or a combination of IL-4 plus IL-2. Treatment was continued for 7 days and then the tumours were removed and weighed. The results showed that IL-4 strongly inhibited tumour growth in 83% of individuals, but complete resolution was observed in only 18%. In the IL-2 treated groups, the percentage of growth-inhibited tumours was markedly less (50%), with 14% complete resolutions. In the IL-4+IL-2 treated tumours resolution was again different, such that only 57% of tumours were smaller than those seen in the controls but there was a high number bearing no measurable tumour (25%). In addition, of the three treatments described, only peritumoural administration of IL-4 alone could mediate the induction of systemic protection from tumour growth. These results suggest that IL-4 and IL-2 have different mechanisms of action and that IL-2 may antagonise the effect of IL-4 such that the action of the two materials when combined is highly unpredictable.
我们研究了白细胞介素-4(IL-4)和白细胞介素-2(IL-2)抑制C57BL/6小鼠B.16黑色素瘤生长的相对能力。待肿瘤形成后,在肿瘤周围给予IL-4或IL-2,或IL-4加IL-2的组合进行治疗。治疗持续7天,然后切除肿瘤并称重。结果显示,IL-4强烈抑制了83%个体的肿瘤生长,但仅18%观察到肿瘤完全消退。在IL-2治疗组中,肿瘤生长受抑制的百分比明显较低(50%),完全消退率为14%。在IL-4 + IL-2治疗的肿瘤中,消退情况又有所不同,只有57%的肿瘤比对照组小,但有大量肿瘤无法测量(25%)。此外,在所描述的三种治疗中,只有单独在肿瘤周围给予IL-4能够介导对肿瘤生长的全身保护诱导。这些结果表明,IL-4和IL-2具有不同的作用机制,并且IL-2可能拮抗IL-4的作用,使得两种物质联合使用时的作用高度不可预测。