Rational design and development of a peptide inhibitor for the PD-1/PD-Ll interaction

被引:40
作者
Boohaker, Rebecca J. [1 ,2 ]
Sambandam, Vijaya [1 ]
Segura, Isaac [3 ]
Miller, James [4 ]
Suto, Mark [1 ]
Xu, Bo [1 ,2 ,5 ]
机构
[1] Southern Res Inst, Drug Discovery Div, Birmingham, AL 35205 USA
[2] Univ Alabama Birmingham, Birmingham Comprehens Canc Ctr, Dept Cell Dev & Integrat Biol, Birmingham, AL 35294 USA
[3] Spring Hill Coll, Dept Chem, Mobile, AL 36608 USA
[4] Wake Forest Univ, Dept Chem, Winston Salem, NC 27109 USA
[5] Tianjin Med Univ Canc Inst & Hosp, Natl Clin Res Ctr Canc, Tianjins Clin Res Ctr Canc, Key Lab Breast Canc Prevent & Therapy,Minist Educ, Tianjin, Peoples R China
关键词
PD-1; Peptide therapy; Immune checkpoints; CD8; T-cells; CELL LUNG-CANCER; DOCK WEB SERVER; PD-1;
D O I
10.1016/j.canlet.2018.04.031
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
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-LI 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 P1120131 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-Ll binding while maintaining CTL viability and activity that can further the development of alternatives to antibody based immunotherapies. (C) 2018 Published by Elsevier B.V.
引用
收藏
页码:11 / 21
页数:11
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