| Autor: |
Jaspers JE; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA., Khan JF; Weill Cornell School of Medicine, New York, New York, USA., Godfrey WD; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA., Lopez AV; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA., Ciampricotti M; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA., Rudin CM; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.; Thoracic Oncology, Memorial Sloan Kettering Cancer Center, New York, New York, USA., Brentjens RJ; Weill Cornell School of Medicine, New York, New York, USA.; Department of Medicine, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA. |
| Abstrakt: |
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. |
