Division of Haematology and Immunology, Leeds Institute of Medical Research, Leeds, UK.
Division of Immunology-Oncology Research Center, Maisonneuve-Rosemont Hospital, Montreal, QC, Canada.
Adv Exp Med Biol. 2019;1164:225-233. doi: 10.1007/978-3-030-22254-3_17.
Immune checkpoint blockade (ICB) has proved successful in the immunotherapeutic treatment of various human cancers. Despite its success, most patients are still not cured while immunogenic cold cancers are still poorly responsive. There is a need for novel clinical interventions in immunotherapy, either alone or in conjunction with ICB. Here, we outline our recent discovery that the intracellular signaling kinase glycogen synthase kinase-3 (GSK-3) is a central regulator of PD-1 in T-cells. We demonstrate the application of small molecule inhibitor (SMI) approaches to down-regulate PD-1 in tumor immunotherapy. GSK-3 SMIs were found as effective as anti-PD-1 in the elimination of melanoma in mouse models. We propose the development of novel SMIs to target co-receptors for the future of immunotherapy.
免疫检查点阻断 (ICB) 已被证明在人类各种癌症的免疫治疗中取得了成功。尽管取得了成功,但大多数患者仍未治愈,而免疫原性冷肿瘤的反应仍然很差。免疫疗法需要新的临床干预措施,无论是单独使用还是与 ICB 联合使用。在这里,我们概述了我们最近的发现,即细胞内信号激酶糖原合酶激酶-3 (GSK-3) 是 T 细胞中 PD-1 的中央调节剂。我们证明了小分子抑制剂 (SMI) 方法在肿瘤免疫治疗中下调 PD-1 的应用。GSK-3 SMI 被发现与抗 PD-1 一样有效,可以消除小鼠模型中的黑色素瘤。我们提出开发针对共受体的新型 SMI,以展望免疫治疗的未来。