The PD-1/PD-L1 Axis and Virus Infections: A Delicate Balance

Front Cell Infect Microbiol. 2019 Jun 13:9:207. doi: 10.3389/fcimb.2019.00207. eCollection 2019.

Abstract

Programmed cell death protein (PD-1) and its ligands play a fundamental role in the evasion of tumor cells from antitumor immunity. Less well appreciated is the fact that the PD-1/PD-L1 axis also regulates antiviral immune responses and is therefore modulated by a number of viruses. Upregulation of PD-1 and its ligands PD-L1 and PD-L2 is observed during acute virus infection and after infection with persistent viruses including important human pathogens such as human immunodeficiency virus (HIV), hepatitis C virus (HCV), and hepatitis B virus (HBV). Experimental evidence suggests that insufficient signaling through the PD-1 pathway promotes immunopathology during acute infection by exaggerating primary T cell responses. If chronic infection is established, however, high levels of PD-1 expression can have unfavorable immunological consequences. Exhaustion and suppression of antiviral immune responses can result in viral immune evasion. The role of the PD-1/PD-L1 axis during viral infections is further complicated by evidence that PD-L1 also mediates inflammatory effects in the acute phase of an immune response. In this review, we discuss the intricate interplay between viruses and the PD-1/PD-L1 axis.

Keywords: PD-1; PD-L1; PD-L2; antiviral immune responses; viral immune evasion; virus-induced immunopathogenesis; viruses.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antiviral Agents
  • B7-H1 Antigen / metabolism*
  • HIV / immunology
  • Hepacivirus / immunology
  • Hepatitis B virus / immunology
  • Humans
  • Immune Evasion
  • Ligands
  • Programmed Cell Death 1 Ligand 2 Protein / metabolism
  • Programmed Cell Death 1 Receptor / metabolism*
  • T-Lymphocytes / immunology
  • Virus Diseases / immunology
  • Virus Diseases / metabolism*

Substances

  • Antiviral Agents
  • B7-H1 Antigen
  • CD274 protein, human
  • Ligands
  • PDCD1 protein, human
  • PDCD1LG2 protein, human
  • Programmed Cell Death 1 Ligand 2 Protein
  • Programmed Cell Death 1 Receptor