PD-L1: Biological mechanism, function, and immunotherapy in gastric cancer

Front Immunol. 2022 Nov 24:13:1060497. doi: 10.3389/fimmu.2022.1060497. eCollection 2022.

Abstract

Gastric cancer (GC) is one of the main causes of cancer incidence rate and mortality worldwide. As the main breakthrough direction, the application of immune checkpoint inhibitors makes patients with GC have better prognosis, where PD-L1/PD-1 inhibitors in immunotherapy have good anti-tumor immune efficacy. Further understanding of the regulatory mechanism of PD-L1 in GC may bring substantial progress to the immunotherapy. In this review, we provide information on the endogenous and exogenous regulatory mechanisms of PD-L1 and its biological functions combined with current clinical trials of PD-L1/PD-1 inhibitors in GC. The malignant biological phenotypes caused by PD-L1 and the corresponding clinical combined treatment scheme have been reported. Identifying the biomarkers of the potential efficacy of immunotherapy and specifying the clinical immunotherapy scheme in combination with molecular characteristics of patients may maximize clinical benefits and better prognosis.

Keywords: clinical trials; gastric cancer; immune checkpoint inhibitor (ICI); programmed death-ligand 1; tumor microenvironment.

Publication types

  • Review

MeSH terms

  • B7-H1 Antigen*
  • Combined Modality Therapy
  • Humans
  • Immune Checkpoint Inhibitors / therapeutic use
  • Immunotherapy
  • Stomach Neoplasms* / therapy

Substances

  • B7-H1 Antigen
  • Immune Checkpoint Inhibitors