Center for Cellular Immunotherapies, Abramson Cancer Center, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104-5156, USA.
Center for Cellular Immunotherapies, Abramson Cancer Center, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104-5156, USA.
Cell Rep. 2017 Sep 26;20(13):3025-3033. doi: 10.1016/j.celrep.2017.09.002.
The effects of transgenically encoded human and mouse IL-18 on T cell proliferation and its application in boosting chimeric antigen receptor (CAR) T cells are presented. Robust enhancement of proliferation of IL-18-secreting human T cells occurred in a xenograft model, and this was dependent on TCR and IL-18R signaling. IL-18 augmented IFN-γ secretion and proliferation of T cells activated by the endogenous TCR. TCR-deficient, human IL-18-expressing CD19 CAR T cells exhibited enhanced proliferation and antitumor activity in the xenograft model. Antigen-propelled activation of cytokine helper ensemble (APACHE) CAR T cells displayed inducible expression of IL-18 and enhanced antitumor immunity. In an intact mouse tumor model, CD19-IL-18 CAR T cells induced deeper B cell aplasia, significantly enhanced CAR T cell proliferation, and effectively augmented antitumor effects in mice with B16F10 melanoma. These findings point to a strategy to develop universal CAR T cells for patients with solid tumors.
本文介绍了转基因人源和鼠源白细胞介素 18(IL-18)对 T 细胞增殖的影响,及其在增强嵌合抗原受体(CAR)T 细胞中的应用。在异种移植模型中,IL-18 分泌的人源 T 细胞的增殖得到了显著增强,这依赖于 TCR 和 IL-18R 信号。IL-18 增强了由内源性 TCR 激活的 T 细胞的 IFN-γ分泌和增殖。在 TCR 缺陷的、表达人源 IL-18 的 CD19 CAR T 细胞的异种移植模型中,表现出增强的增殖和抗肿瘤活性。抗原驱动的细胞因子辅助复合物(APACHE)CAR T 细胞表现出可诱导的 IL-18 表达和增强的抗肿瘤免疫。在完整的小鼠肿瘤模型中,CD19-IL-18 CAR T 细胞诱导更深的 B 细胞耗竭,显著增强了 CAR T 细胞的增殖,并有效地增强了患有 B16F10 黑色素瘤小鼠的抗肿瘤效果。这些发现为开发用于实体瘤患者的通用 CAR T 细胞提供了一种策略。