Rational design and development of a peptide inhibitor for the PD-1/PD-L1 interaction.

Cancer Lett

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; Key Laboratory of Breast Cancer Prevention and Therapy, Ministry of Education, Tianjin's Clinical Research Center for Cancer, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Tianjin, China. Electronic address:

Published: October 2018

AI Article Synopsis

  • Researchers developed a peptide inhibitor, PL120131, to target the PD-1/PD-L1 interaction as a potential alternative to current antibody treatments.
  • The peptide was shown to bind to PD-1 and effectively inhibit the PD-1 signaling pathway, preventing apoptosis in immune cells like Jurkat cells and primary lymphocytes.
  • PL120131 demonstrated superior performance in enhancing T cell activity and survivability in a 3D co-culture model compared to traditional anti-PD-1 antibodies, highlighting its potential for advancing immunotherapy approaches.

Article Abstract

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.

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http://dx.doi.org/10.1016/j.canlet.2018.04.031DOI Listing

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