Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387 Krakow, Poland.
Department of Clinical Immunology, Institute of Pediatrics, Jagiellonian University Medical College, Wielicka 265, 30-663 Krakow, Poland.
Molecules. 2019 Aug 1;24(15):2804. doi: 10.3390/molecules24152804.
is currently the only small-molecule modulator in clinical trials targeting PD-L1 and VISTA proteins - important negative checkpoint regulators of immune activation. The reported therapeutic results to some extent mimic those of FDA-approved monoclonal antibodies overcoming the limitations of the high production costs and adverse effects of the latter. However, no conclusive biophysical evidence proving the binding to hPD-L1 has ever been presented. Using well-known in vitro methods: NMR binding assay, HTRF and cell-based activation assays, we clearly show that there is no direct binding between and PD-L1. To strengthen our reasoning, we performed control experiments on - a 29-mer peptide, which is a precursor of . Positive controls consisted of the well-documented small-molecule PD-L1 inhibitors: and .
目前,它是唯一一款针对 PD-L1 和 VISTA 蛋白的临床研究中的小分子调节剂——这些蛋白是免疫激活的重要负性检查点调节剂。报道的治疗结果在某种程度上模拟了 FDA 批准的单克隆抗体的治疗效果,克服了后者生产成本高和副作用大的限制。然而,从未有过证明与 hPD-L1 结合的明确的生物物理证据。我们使用众所周知的体外方法:NMR 结合测定法、HTRF 和基于细胞的激活测定法,清楚地表明 与 PD-L1 之间没有直接结合。为了加强我们的推理,我们对 进行了对照实验, 是 29 肽,是 的前体。阳性对照由有充分文献记载的小分子 PD-L1 抑制剂组成: 和 。