Southern Research Institute, Drug Discovery Division, Birmingham, AL, 35205, USA; University of Alabama at Birmingham Comprehensive Cancer Center, Department of Cell, Developmental and Integrative Biology, Birmingham, AL, 35294, USA.
Southern Research Institute, Drug Discovery Division, Birmingham, AL, 35205, USA.
Cancer Lett. 2018 Oct 10;434:11-21. doi: 10.1016/j.canlet.2018.04.031. Epub 2018 Jun 18.
We report here the rational design and validation of a peptide inhibitor to the PD-1/PD-L1 interaction as an attempt to develop a viable alternative to current inhibitory antibodies. We demonstrated, by biolayer interferometry and in silico docking simulations, that a PD-L1 peptide mimetic (PL120131) can interfere with the PD-1/PD-L1 interaction by binding to PD-1. We show that PL120131 is capable of inhibiting PD-1 mediated apoptotic signaling pathway and rescuing Jurkat cells and primary lymphocytes from apoptosis. Additionally, we show that PL120131 treatment allows for CTL anti-tumor activity. Furthermore, PL120131 can maintain co-culture survivability and activity of T Cells in a 3D co-culture model better than the anti-PD-1 blocking antibody. Together, the characterization of this PD-1/PD-L1 inhibiting peptide provides insight regarding the ability to inhibit PD-L1 binding while maintaining CTL viability and activity that can further the development of alternatives to antibody based immunotherapies.
我们在此报告了一种针对 PD-1/PD-L1 相互作用的肽抑制剂的合理设计和验证,试图开发一种可行的替代当前抑制性抗体的方法。我们通过生物层干涉法和计算机对接模拟证明,一种 PD-L1 肽模拟物(PL120131)可以通过与 PD-1 结合来干扰 PD-1/PD-L1 相互作用。我们表明,PL120131 能够抑制 PD-1 介导的凋亡信号通路,并挽救 Jurkat 细胞和原代淋巴细胞免于凋亡。此外,我们表明,PL120131 治疗允许 CTL 抗肿瘤活性。此外,PL120131 可以在 3D 共培养模型中比抗 PD-1 阻断抗体更好地维持共培养细胞的存活率和 T 细胞的活性。总之,这种 PD-1/PD-L1 抑制肽的特性提供了关于抑制 PD-L1 结合的能力的见解,同时保持 CTL 的活力和活性,这可以进一步开发替代抗体为基础的免疫疗法。