PD-1/PD-L1 in disease

Immunotherapy. 2018 Feb;10(2):149-160. doi: 10.2217/imt-2017-0120.

Abstract

Aim: Expression of PD-1 on T/B cells regulates peripheral tolerance and autoimmunity. Binding of PD-1 to its ligand, PD-L1, leads to protection against self-reactivity. In contrary, tumor cells have evolved immune escape mechanisms whereby overexpression of PD-L1 induces anergy and/or apoptosis of PD-1 positive T cells by interfering with T cell receptor signal transduction. PD-L1 and PD-1 blockade using antibodies are in human clinical trials as an alternative cancer treatment modality. Areas covered: We describe the role of PD-1/PD-L1 in disease in the context of autoimmunity, neurological disorders, stroke and cancer.

Conclusion: For immunotherapy/vaccines to be successful, the expression of PD-L1/PD-1 on immune cells should be considered, and the combination of checkpoint inhibitors and vaccines may pave the way for successful outcomes to disease.

Keywords: PD-1; PD-L1; autoimmune disease; cancer; neurological disease; vaccines.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / therapeutic use*
  • Autoimmunity
  • B7-H1 Antigen / antagonists & inhibitors
  • B7-H1 Antigen / immunology
  • Cancer Vaccines / immunology*
  • Humans
  • Immunotherapy / methods*
  • Lymphocyte Activation
  • Neoplasms / immunology
  • Neoplasms / therapy*
  • Nervous System Diseases / immunology
  • Nervous System Diseases / therapy*
  • Programmed Cell Death 1 Receptor / antagonists & inhibitors
  • Programmed Cell Death 1 Receptor / immunology
  • Signal Transduction
  • Stroke / immunology
  • Stroke / therapy*
  • T-Lymphocytes / immunology*
  • Tumor Escape

Substances

  • Antibodies, Monoclonal
  • B7-H1 Antigen
  • Cancer Vaccines
  • PDCD1 protein, human
  • Programmed Cell Death 1 Receptor