A novel bispecific peptide targeting PD-1 and PD-L1 with combined antitumor activity of T-cells derived from the patients with TSCC

Int Immunopharmacol. 2024 Sep 10:138:112582. doi: 10.1016/j.intimp.2024.112582. Epub 2024 Jul 8.

Abstract

Programmed death-1 (PD-1) and programmed death ligand-1 (PD-L1) are key immune checkpoints (ICs) that critically influence immunotherapy. Tumor resistance to single IC-targeting drugs has increased interest in dual-target drugs, which have shown feasibility for cancer treatment. In this study, we aimed to develop dual-target peptide drugs targeting the PD-1/PD-L1 pathway and to evaluate their efficacy compared to functional antibodies in enhancing the cytotoxicity of human T cells against tongue squamous carcinoma cell lines. Through sequence analysis and peptide truncation, we modified a pre-existing peptide named nABPD-1 targeting PD-1. Subsequently, we obtained two novel peptides named nABPD-2 and nABPD-3, with nABPD-2 showing an enhanced affinity for human PD-1 protein compared to nABPD-1. Importantly, nABPD-2 exhibited dual-targeting capability, possessing a high affinity for both PD-L1 and PD-1. Furthermore, nABPD-2 effectively promoted the cytotoxicity of human T cells against tongue squamous carcinoma cell lines, surpassing the efficacy of anti-PD-1 or anti-PD-L1 functional antibodies alone. Considering that nABPD-2 has lower production costs and dose requirements, it can potentially be used in therapeutic applications.

Keywords: Bispecific peptides; Cancer immunotherapy; PD-1, PD-L1; Tongue squamous cell carcinoma (TSCC).

MeSH terms

  • B7-H1 Antigen* / antagonists & inhibitors
  • Carcinoma, Squamous Cell* / drug therapy
  • Cell Line, Tumor
  • Humans
  • Immune Checkpoint Inhibitors / pharmacology
  • Immunotherapy / methods
  • Peptides* / pharmacology
  • Programmed Cell Death 1 Receptor* / antagonists & inhibitors
  • T-Lymphocytes / immunology
  • Tongue Neoplasms* / drug therapy

Substances

  • B7-H1 Antigen
  • CD274 protein, human
  • Immune Checkpoint Inhibitors
  • PDCD1 protein, human
  • Peptides
  • Programmed Cell Death 1 Receptor