Division of Urology, Department of Surgery, Cedars-Sinai Medical Center, 8635 West 3rd Street, Suite 1070W, Los Angeles, CA 90048, USA.
Br J Cancer. 2011 Feb 15;104(4):643-52. doi: 10.1038/bjc.2011.15. Epub 2011 Feb 1.
Temsirolimus is a mammalian target of rapamycin (mTOR) inhibitor and rapamycin analogue that is approved for treating advanced renal cell carcinoma (RCC). It is being actively evaluated in clinical trials for melanoma. The mTOR inhibitors are also immunosuppressants and are used clinically to prevent rejection following solid-organ transplant. Novel immunotherapies are being actively developed for immunoresponsive tumours, such as RCC and melanoma.
Immune-modulating effects of temsirolimus were characterised when used in combination with cancer vaccines targeting RCC (RENCA) and melanoma (B16). Cancer vaccines were recombinant tumour-specific proteins (CA9 or gp100), and recombinant heat shock protein (HSP; hsp110) served as the immune adjuvant.
In murine models, temsirolimus enhanced the anti-tumour activity of cancer vaccines used to treat established RENCA and B16 tumours. A tumour prevention model established that the enhanced anti-tumour activity associated with temsirolimus was immune mediated. In mice treated with an HSP-based anti-tumour vaccine, temsirolimus-treated CD8 T cells had greater interferon-γ and cytotoxic T-cell responses when compared with mice treated with vaccine alone. Temsirolimus also enhanced the formation of CD8 memory cells following administration of HSP-based cancer vaccine.
These results provide a rationale for combining mTOR inhibitor with immunotherapy when treating immunoresponsive tumours.
替西罗莫司是一种哺乳动物雷帕霉素靶蛋白(mTOR)抑制剂和雷帕霉素类似物,已被批准用于治疗晚期肾细胞癌(RCC)。它正在临床试验中积极评估用于黑色素瘤。mTOR 抑制剂也是免疫抑制剂,临床上用于预防实体器官移植后的排斥反应。新型免疫疗法正在积极开发用于免疫反应性肿瘤,如 RCC 和黑色素瘤。
当替西罗莫司与针对 RCC(RENCA)和黑色素瘤(B16)的癌症疫苗联合使用时,其免疫调节作用得到了表征。癌症疫苗是重组肿瘤特异性蛋白(CA9 或 gp100),重组热休克蛋白(HSP;hsp110)用作免疫佐剂。
在小鼠模型中,替西罗莫司增强了用于治疗已建立的 RENCA 和 B16 肿瘤的癌症疫苗的抗肿瘤活性。建立了肿瘤预防模型,表明替西罗莫司相关的增强抗肿瘤活性是免疫介导的。在接受 HSP 为基础的抗肿瘤疫苗治疗的小鼠中,与单独接受疫苗治疗的小鼠相比,替西罗莫司治疗的 CD8 T 细胞具有更高的干扰素-γ 和细胞毒性 T 细胞反应。替西罗莫司还增强了 HSP 为基础的癌症疫苗给药后 CD8 记忆细胞的形成。
这些结果为在治疗免疫反应性肿瘤时将 mTOR 抑制剂与免疫疗法联合使用提供了依据。