Engineered nanomedicines block the PD-1/PD-L1 axis for potentiated cancer immunotherapy

Acta Pharmacol Sin. 2022 Nov;43(11):2749-2758. doi: 10.1038/s41401-022-00910-w. Epub 2022 Apr 28.

Abstract

Immunotherapy, in particular immune checkpoint blockade (ICB) therapy targeting the programmed cell death-1 (PD-1)/programmed cell death ligand-1 (PD-L1) axis, has remarkably revolutionized cancer treatment in the clinic. Anti-PD-1/PD-L1 therapy is designed to restore the antitumor response of cytotoxic T cells (CTLs) by blocking the interaction between PD-L1 on tumour cells and PD-1 on CTLs. Nevertheless, current anti-PD-1/PD-L1 therapy suffers from poor therapeutic outcomes in a large variety of solid tumours due to insufficient tumour specificity, severe cytotoxic effects, and the occurrence of immune resistance. In recent years, nanosized drug delivery systems (NDDSs), endowed with highly efficient tumour targeting and versatility for combination therapy, have paved a new avenue for cancer immunotherapy. In this review article, we summarized the recent advances in NDDSs for anti-PD-1/PD-L1 therapy. We then discussed the challenges and further provided perspectives to promote the clinical application of NDDS-based anti-PD-1/PD-L1 therapy.

Keywords: PD-1/PD-L1 axis; cancer immunotherapy; immune checkpoint blockade; nanomedicine; nanosized drug delivery systems..

Publication types

  • Review

MeSH terms

  • B7-H1 Antigen* / metabolism
  • Humans
  • Immunotherapy
  • Nanomedicine
  • Neoplasms* / therapy
  • Programmed Cell Death 1 Receptor

Substances

  • B7-H1 Antigen
  • Programmed Cell Death 1 Receptor