コンテンツへスキップ
Merck

Targeting REGNASE-1 programs long-lived effector T cells for cancer therapy.

Nature (2019-12-13)
Jun Wei, Lingyun Long, Wenting Zheng, Yogesh Dhungana, Seon Ah Lim, Cliff Guy, Yanyan Wang, Yong-Dong Wang, Chenxi Qian, Beisi Xu, Anil Kc, Jordy Saravia, Hongling Huang, Jiyang Yu, John G Doench, Terrence L Geiger, Hongbo Chi
要旨

Adoptive cell therapy represents a new paradigm in cancer immunotherapy, but it can be limited by the poor persistence and function of transferred T cells1. Here we use an in vivo pooled CRISPR-Cas9 mutagenesis screening approach to demonstrate that, by targeting REGNASE-1, CD8+ T cells are reprogrammed to long-lived effector cells with extensive accumulation, better persistence and robust effector function in tumours. REGNASE-1-deficient CD8+ T cells show markedly improved therapeutic efficacy against mouse models of melanoma and leukaemia. By using a secondary genome-scale CRISPR-Cas9 screening, we identify BATF as the key target of REGNASE-1 and as a rheostat that shapes antitumour responses. Loss of BATF suppresses the increased accumulation and mitochondrial fitness of REGNASE-1-deficient CD8+ T cells. By contrast, the targeting of additional signalling factors-including PTPN2 and SOCS1-improves the therapeutic efficacy of REGNASE-1-deficient CD8+ T cells. Our findings suggest that T cell persistence and effector function can be coordinated in tumour immunity and point to avenues for improving the efficacy of adoptive cell therapy for cancer.

材料
製品番号
ブランド
製品内容

Sigma-Aldrich
カルボニルシアニド 4-(トリフルオロメトキシ)フェニルヒドラゾン, ≥98% (TLC), powder
Sigma-Aldrich
抗Tom20/Tomm20抗体、クローン2F8.1, clone 2F8.1, from mouse