Johnson Erik E, Yamane Brett H, Buhtoiarov Ilia N, Lum Hillary D, Rakhmilevich Alexander L, Mahvi David M, Gillies Stephen D, Sondel Paul M
Departments of Surgery, Human Oncology, and Pediatrics and Paul P. Carbone Comprehensive Cancer Center, University of Wisconsin, Madison, WI 53792, USA.
Clin Cancer Res. 2009 Aug 1;15(15):4875-84. doi: 10.1158/1078-0432.CCR-09-0110. Epub 2009 Jul 28.
Radiofrequency ablation (RFA) is a common treatment modality for surgically unresectable tumors. However, there is a high rate of both local and systemic recurrence.
In this preclinical study, we sought to enhance the antitumor effect of RFA by combining it with huKS-IL2 immunocytokine [tumor-specific monoclonal antibody fused to interleukin-2 (IL2)] in mice bearing CT26-KS colon adenocarcinoma. Mice were treated with RFA, huKS-IL2 via intratumoral injection, or combination therapy.
Treatment of mice bearing s.c. tumors with RFA and huKS-IL2 resulted in significantly greater tumor growth suppression and enhanced survival compared with mice treated with RFA or huKS-IL2 alone. When subtherapeutic regimens of RFA or huKS-IL2 were used, tumors progressed in all treated mice. In contrast, the combination of RFA and immunocytokine resulted in complete tumor resolution in 50% of mice. Treatment of a tumor with RFA and intratumoral huKS-IL2 also showed antitumor effects against a distant untreated tumor. Tumor-free mice after treatment with RFA and huKS-IL2 showed immunologic memory based on their ability to reject subsequent challenges of CT26-KS and the more aggressive parental CT26 tumors. Flow cytometry analysis of tumor-reactive T cells from mice with complete tumor resolution showed that treatment with RFA and huKS-IL2 resulted in a greater proportion of cytokine-producing CD4 T cells and CD8 T cells compared with mice treated with RFA or huKS-IL2 alone.
These results show that the addition of huKS-IL2 to RFA significantly enhances the antitumor response in this murine model, resulting in complete tumor resolution and induction of immunologic memory.
射频消融(RFA)是治疗无法手术切除肿瘤的常用方法。然而,局部和全身复发率都很高。
在这项临床前研究中,我们试图通过将RFA与huKS-IL2免疫细胞因子[与白细胞介素-2(IL2)融合的肿瘤特异性单克隆抗体]联合应用于携带CT26-KS结肠腺癌的小鼠,来增强RFA的抗肿瘤效果。小鼠分别接受RFA、瘤内注射huKS-IL2或联合治疗。
与单独接受RFA或huKS-IL2治疗的小鼠相比,用RFA和huKS-IL2治疗皮下肿瘤的小鼠肿瘤生长抑制作用显著增强,生存期延长。当使用RFA或huKS-IL2的亚治疗方案时,所有接受治疗的小鼠肿瘤均进展。相反,RFA与免疫细胞因子联合使用使50%的小鼠肿瘤完全消退。用RFA和瘤内注射huKS-IL2治疗肿瘤也显示出对远处未治疗肿瘤的抗肿瘤作用。接受RFA和huKS-IL2治疗后无瘤小鼠表现出免疫记忆,基于它们排斥随后CT26-KS和更具侵袭性的亲本CT26肿瘤攻击的能力。对肿瘤完全消退小鼠的肿瘤反应性T细胞进行流式细胞术分析表明,与单独接受RFA或huKS-IL2治疗的小鼠相比,用RFA和huKS-IL2治疗导致产生细胞因子的CD4 T细胞和CD8 T细胞比例更高。
这些结果表明,在RFA中添加huKS-IL2可显著增强该小鼠模型中的抗肿瘤反应,导致肿瘤完全消退并诱导免疫记忆。