Cheeloo College of Medicine, Shandong University, Jinan, China.
Department of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, China.
Front Immunol. 2020 May 29;11:1088. doi: 10.3389/fimmu.2020.01088. eCollection 2020.
Programmed cell death protein-1/ligand 1 (PD-1/L1) targeted immune checkpoint inhibitors have become the focus of tumor treatment due to their promising efficacy. Currently, several PD-1/PD-L1 inhibitors have been approved for clinical practice with several more in clinical trials. Notably, based on available trial data, the selection of different PD-1/PD-L1 inhibitors in the therapeutic application and the corresponding efficacy varies. Widespread attention then is increasingly raised to the clinical comparability of different PD-1/PD-L1 inhibitors. The comparison of the inhibitors could not only help clinicians make in-depth understanding of them, but also further facilitate the selection of the optimal inhibitor for patients in treatment as well as for future clinical research and the development of new related drugs. As we all know, molecular structure could determine molecular function, which further affects their application. Therefore, in this review, we aim to comprehensively compare the structural basis, molecular biological functions, and clinical practice of different PD-1/PD-L1 inhibitors.
程序性死亡蛋白-1/配体 1(PD-1/L1)靶向免疫检查点抑制剂由于其疗效显著,成为肿瘤治疗的焦点。目前,已有多种 PD-1/PD-L1 抑制剂获得临床批准,还有更多的处于临床试验阶段。值得注意的是,基于现有试验数据,不同 PD-1/PD-L1 抑制剂在治疗应用中的选择和相应疗效存在差异。因此,不同 PD-1/PD-L1 抑制剂的临床可比性引起了广泛关注。这些抑制剂的比较不仅有助于临床医生深入了解它们,还可以进一步促进为治疗中的患者选择最佳抑制剂,并为未来的临床研究和新的相关药物的开发提供便利。众所周知,分子结构可以决定分子功能,进而影响它们的应用。因此,在这篇综述中,我们旨在全面比较不同 PD-1/PD-L1 抑制剂的结构基础、分子生物学功能和临床实践。