Targeting PD-L1 in non-small cell lung cancer using CAR T cells.
Ming LiuXu WangWei LiXinfang YuPedro Flores-VillanuevaZijun Y Xu-MonetteLing LiMingzhi ZhangKen H H YoungXiaodong MaYong LiPublished in: Oncogenesis (2020)
Antibodies against programmed cell death protein 1 (PD-1) and its ligand (PD-L1) have dramatically changed the landscape of therapies for non-small cell lung carcinoma (NSCLC); however, the majority of patients do not respond to these agents. In addition, hyperprogressive disease (HPD) develops in a larger portion of NSCLC patients treated with PD-1/PD-L1 inhibitors than in patients treated with standard chemotherapy. The use of chimeric antigen receptor (CAR) T cells has been successful to treat blood cancers but not for solid tumors like NSCLC. In this work, we constructed CAR T cells that target PD-L1 and evaluated their efficacy in NSCLC with either high or low PD-L1 expression. PD-L1-CAR T cells exhibited antigen-specific activation, cytokine production, and cytotoxic activity against PD-L1high NSCLC cells and xenograft tumors. Furthermore, the addition of a subtherapeutic dose of local radiotherapy improved the efficacy of PD-L1-CAR T cells against PD-L1low NSCLC cells and tumors. Our findings indicate that PD-L1-CAR T cells represent a novel therapeutic strategy for patients with PD-L1-positive NSCLC, particularly for those who are susceptible to HPD.
Keyphrases
- small cell lung cancer
- advanced non small cell lung cancer
- induced apoptosis
- cell cycle arrest
- brain metastases
- end stage renal disease
- endoplasmic reticulum stress
- early stage
- ejection fraction
- epidermal growth factor receptor
- signaling pathway
- newly diagnosed
- single cell
- radiation therapy
- chronic kidney disease
- pi k akt
- cell therapy
- squamous cell carcinoma
- wastewater treatment
- bone marrow
- small molecule
- patient reported
- peritoneal dialysis
- protein protein
- chemotherapy induced