PD1/PD-L1 immune checkpoint as a potential target for preventing brain tumor progression

Cancer Immunol Immunother. 2022 Sep;71(9):2067-2075. doi: 10.1007/s00262-021-03130-z. Epub 2022 Jan 29.

Abstract

Programmed death-1 (PD-1) is a cell surface receptor that functions as a T cell checkpoint and plays a central role in regulating T cell collapse. The binding of PD-1 to its ligand programmed death-ligand 1 (PD-L1) activates downstream signaling pathways and inhibits T cell activation in the perspective of immune system mechanism and regulation in tumor progression. It is well reported that tumors adopt certain immune-checkpoint pathways as a mechanism of resistance against immune cells such as T cells that are specific for tumor antigens. Indeed, the PD-1/PD-L1 pathway controls the induction and maintenance of immune tolerance within the tumor microenvironment. Thus, the PD-1/PD-L1 checkpoint regulation appears to be of extreme importance as well as the immunotherapy targeting that via and the using of PD-1/PD-L1 inhibitors that have changed the scenario of brain cancer treatment and survival. Here, we review the mechanism of action of PD-1 and PD-L1, the PD/PDL-1 signaling pathway involved in the progression of brain tumors, and its application as cancer immunotherapy counteracting tumor escape in central nervous system.

Keywords: Brain tumor; CNS; Immune system; Immunotherapy; PD/PDL-1 pathway.

Publication types

  • Review

MeSH terms

  • B7-H1 Antigen* / metabolism
  • Brain Neoplasms* / therapy
  • Humans
  • Immune Checkpoint Proteins* / metabolism
  • Immunotherapy
  • Programmed Cell Death 1 Receptor* / metabolism
  • Tumor Microenvironment

Substances

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