Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Weill Cornell School of Medicine, New York, New York, USA.
J Clin Invest. 2023 May 1;133(9):e166028. doi: 10.1172/JCI166028.
Patients with small cell lung cancer (SCLC) generally have a poor prognosis and a median overall survival of only about 13 months, indicating the urgent need for novel therapies. Delta-like protein 3 (DLL3) has been identified as a tumor-specific cell surface marker on neuroendocrine cancers, including SCLC. In this study, we developed a chimeric antigen receptor (CAR) against DLL3 that displays antitumor efficacy in xenograft and murine SCLC models. CAR T cell expression of the proinflammatory cytokine IL-18 greatly enhanced the potency of DLL3-targeting CAR T cell therapy. In a murine metastatic SCLC model, IL-18 production increased the activation of both CAR T cells and endogenous tumor-infiltrating lymphocytes. We also observed an increased infiltration, repolarization, and activation of antigen-presenting cells. Additionally, human IL-18-secreting anti-DLL3 CAR T cells showed an increased memory phenotype, less exhaustion, and induced durable responses in multiple SCLC models, an effect that could be further enhanced with anti-PD-1 blockade. All together, these results define DLL3-targeting CAR T cells that produce IL-18 as a potentially promising novel strategy against DLL3-expressing solid tumors.
患有小细胞肺癌 (SCLC) 的患者通常预后较差,中位总生存期仅约 13 个月,表明迫切需要新的治疗方法。Delta-like 蛋白 3 (DLL3) 已被确定为神经内分泌癌(包括 SCLC)的肿瘤特异性细胞表面标志物。在这项研究中,我们开发了一种针对 DLL3 的嵌合抗原受体 (CAR),在异种移植和小鼠 SCLC 模型中显示出抗肿瘤疗效。CAR T 细胞表达促炎细胞因子 IL-18 极大地增强了 DLL3 靶向 CAR T 细胞治疗的效力。在小鼠转移性 SCLC 模型中,IL-18 的产生增加了 CAR T 细胞和内源性肿瘤浸润淋巴细胞的激活。我们还观察到抗原呈递细胞的浸润、重极化和激活增加。此外,分泌人 IL-18 的抗-DLL3 CAR T 细胞表现出增加的记忆表型、更少的衰竭,并在多种 SCLC 模型中诱导持久反应,这种效果可以通过抗 PD-1 阻断进一步增强。总而言之,这些结果定义了产生 IL-18 的靶向 DLL3 的 CAR T 细胞作为一种针对表达 DLL3 的实体瘤的潜在有前途的新策略。