IFOM, FIRC Institute of Molecular Oncology, Milan 20139, Italy.
Laboratory of Hematology-Oncology, European Institute of Oncology IRCCS, Milan 20141, Italy.
Cell Rep. 2022 Aug 23;40(8):111256. doi: 10.1016/j.celrep.2022.111256.
Immunotherapy is improving the prognosis and survival of cancer patients, but despite encouraging outcomes in different cancers, the majority of tumors are resistant to it, and the immunotherapy combinations are often accompanied by severe side effects. Here, we show that a periodic fasting-mimicking diet (FMD) can act on the tumor microenvironment and increase the efficacy of immunotherapy (anti-PD-L1 and anti-OX40) against the poorly immunogenic triple-negative breast tumors (TNBCs) by expanding early exhausted effector T cells, switching the cancer metabolism from glycolytic to respiratory, and reducing collagen deposition. Furthermore, FMD reduces the occurrence of immune-related adverse events (irAEs) by preventing the hyperactivation of the immune response. These results indicate that FMD cycles have the potential to enhance the efficacy of anti-cancer immune responses, expand the portion of tumors sensitive to immunotherapy, and reduce its side effects.
免疫疗法正在改善癌症患者的预后和生存率,但尽管在不同癌症中取得了令人鼓舞的结果,大多数肿瘤仍然对其具有抗性,而且免疫疗法组合常常伴随着严重的副作用。在这里,我们表明,周期性禁食模拟饮食(FMD)可以通过扩展早期耗竭效应 T 细胞、将癌症代谢从糖酵解转变为呼吸作用以及减少胶原蛋白沉积来作用于肿瘤微环境,从而提高免疫疗法(抗 PD-L1 和抗 OX40)对免疫原性差的三阴性乳腺癌(TNBC)的疗效。此外,FMD 通过防止免疫反应的过度激活来降低免疫相关不良事件(irAEs)的发生。这些结果表明,FMD 周期有可能增强抗癌免疫反应的疗效,扩大对免疫疗法敏感的肿瘤部分,并降低其副作用。