Department of Medical Biotechnology, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran; Cellular and Molecular Biology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Department of Anatomy, School of Medicine, Kurdistan University of Medical Sciences, Sanandaj, Iran.
Life Sci. 2024 Feb 1;338:122387. doi: 10.1016/j.lfs.2023.122387. Epub 2023 Dec 26.
Chimeric antigen receptor-modified T (CAR-T) are genetically engineered cells to express tumor-specific antigens revolutionizing the treatment of hematologic malignancies. The hostile tumor microenvironment (TME) remains a challenge for CAR-T cell therapy in solid tumors. As a solution, combinational therapy with immune checkpoint inhibitors (ICIs) is shown to improve the safety and efficacy of CAR-T cell therapy. To avoid side effects related to the application of ICIs in combinational therapy, engineering CARs to express tumor-specific antigens may help improvement of clinical outcomes. Those CARs expressing single chain variable fragments (scFvs) or nanobodies against immune checkpoint stimulatory or inhibitory molecules, such as the programmed death-1 (PD-1)/programmed death-ligand 1 (PD-L1) signaling axis are being extensively studied in various clinical trials. In this review, we discuss the significance of anti-PD-(L)1 scFv-expressing CAR-T cells in the treatment of human cancers, describing current challenges and potential strategies to overcome such predicaments in the area of cancer immunotherapy.
嵌合抗原受体修饰的 T 细胞(CAR-T)是表达肿瘤特异性抗原的基因工程细胞,彻底改变了血液恶性肿瘤的治疗方法。但在实体肿瘤中,CAR-T 细胞疗法仍面临着恶劣的肿瘤微环境(TME)的挑战。作为一种解决方案,联合免疫检查点抑制剂(ICIs)的治疗已被证明可以提高 CAR-T 细胞治疗的安全性和疗效。为了避免与 ICI 联合治疗相关的副作用,可以通过工程 CAR 来表达肿瘤特异性抗原,从而有助于改善临床结果。目前正在各种临床试验中广泛研究表达针对免疫检查点刺激或抑制分子的单链可变片段(scFv)或纳米抗体的 CAR,例如程序性死亡受体 1(PD-1)/程序性死亡配体 1(PD-L1)信号轴。在这篇综述中,我们讨论了抗 PD-(L)1 scFv 表达的 CAR-T 细胞在人类癌症治疗中的重要性,描述了当前的挑战和潜在策略,以克服癌症免疫治疗领域的这些困境。