Programmed death ligand 2 in cancer-induced immune suppression

Clin Dev Immunol. 2012:2012:656340. doi: 10.1155/2012/656340. Epub 2012 Apr 29.

Abstract

Inhibitory molecules of the B7/CD28 family play a key role in the induction of immune tolerance in the tumor microenvironment. The programmed death-1 receptor (PD-1), with its ligands PD-L1 and PD-L2, constitutes an important member of these inhibitory pathways. The relevance of the PD-1/PD-L1 pathway in cancer has been extensively studied and therapeutic approaches targeting PD-1 and PD-L1 have been developed and are undergoing human clinical testing. However, PD-L2 has not received as much attention and its role in modulating tumor immunity is less clear. Here, we review the literature on the immunobiology of PD-L2, particularly on its possible roles in cancer-induced immune suppression and we discuss the results of recent studies targeting PD-L2 in cancer.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / therapeutic use
  • Clinical Trials as Topic
  • Humans
  • Immunosuppression Therapy*
  • Mice
  • Molecular Targeted Therapy / trends
  • Neoplasms / drug therapy
  • Neoplasms / immunology*
  • Programmed Cell Death 1 Ligand 2 Protein / immunology*
  • Tumor Escape
  • Tumor Microenvironment

Substances

  • Antineoplastic Agents
  • Programmed Cell Death 1 Ligand 2 Protein