IFOM, The AIRC Institute of Molecular Oncology, 20139, Milan, Italy.
Laboratory of Pre-Clinical and Translational Research, IRCCS-CROB, Referral Cancer Center of Basilicata, 85028, Rionero in Vulture, Italy.
Nat Commun. 2023 Sep 8;14(1):5529. doi: 10.1038/s41467-023-41066-3.
Immune checkpoint inhibitors cause side effects ranging from autoimmune endocrine disorders to severe cardiotoxicity. Periodic Fasting mimicking diet (FMD) cycles are emerging as promising enhancers of a wide range of cancer therapies including immunotherapy. Here, either FMD cycles alone or in combination with anti-OX40/anti-PD-L1 are much more effective than immune checkpoint inhibitors alone in delaying melanoma growth in mice. FMD cycles in combination with anti-OX40/anti-PD-L1 also show a trend for increased effects against a lung cancer model. As importantly, the cardiac fibrosis, necrosis and hypertrophy caused by immune checkpoint inhibitors are prevented/reversed by FMD treatment in both cancer models whereas immune infiltration of CD3 and CD8 cells in myocardial tissues and systemic and myocardial markers of oxidative stress and inflammation are reduced. These results indicate that FMD cycles in combination with immunotherapy can delay cancer growth while reducing side effects including cardiotoxicity.
免疫检查点抑制剂会引起从自身免疫内分泌紊乱到严重的心脏毒性等副作用。定期模拟禁食(Fasting mimicking diet,FMD)周期作为多种癌症治疗方法(包括免疫疗法)的有前途的增强剂正在出现。在这里,FMD 周期单独或与抗 OX40/抗 PD-L1 联合使用,比单独使用免疫检查点抑制剂更能有效延缓小鼠黑色素瘤的生长。FMD 周期与抗 OX40/抗 PD-L1 联合使用也显示出对肺癌模型的效果增强趋势。同样重要的是,在这两种癌症模型中,FMD 治疗可预防/逆转免疫检查点抑制剂引起的心脏纤维化、坏死和肥大,而心肌组织中 CD3 和 CD8 细胞的免疫浸润以及系统性和心肌氧化应激和炎症标志物则减少。这些结果表明,FMD 周期与免疫疗法联合使用可以延缓癌症生长,同时减少包括心脏毒性在内的副作用。