医学
封锁
易普利姆玛
结肠炎
肿瘤坏死因子α
免疫疗法
免疫检查点
免疫学
无容量
促炎细胞因子
免疫系统
内科学
炎症
受体
作者
Maite Álvarez,Itziar Otano,Luna Minute,María Carmen Ochoa,Elísabeth Pérez-Ruiz,Ignacio Melero,Pedro Berraondo
出处
期刊:Cell stress
[Shared Science Publishers OG]
日期:2019-07-03
卷期号:3 (7): 236-239
被引量:21
标识
DOI:10.15698/cst2019.07.193
摘要
, Nature 569(7756): 428-432.), we analyzed the potential impact of prophylactic TNF neutralization therapy in the anti-PD1/CTLA-4 efficacy. Through several mouse models, we demonstrated that TNF neutralization ameliorated ICB-exacerbated colitis in addition to improving ICB-dependent anti-tumor efficacy. Similar results were obtained after prophylactic TNF blockade in graft vs host xenografted mouse models with human immune cells, which showed a reduction in colitis and hepatitis. Importantly, there was a preservation of the immunotherapeutic control of xenografted tumors after ICB treatment. Moreover, TNF and TNF-dependent gene expression is upregulated in the colon mucosa from patients affected by colitis as a side effect of ipilimumab and nivolumab. Our results, thus, provide evidence of the successful combination of prophylactic TNF neutralization with ICB therapy strategy to ameliorate toxicities, while keeping or even ameliorating anti-tumor efficacy. The prophylactic TNF blockade strategy is clinically feasible since excellent TNF inhibitors have been approved for the treatment of autoimmunity and are used for the immune-related serious adverse events in immunotherapy.
科研通智能强力驱动
Strongly Powered by AbleSci AI