PD-1 and PD-L1 in cancer immunotherapy: clinical implications and future considerations

Yongshuai Jiang1, Ming Chen2, Hong Nie1,3

  • 1a Shanghai Institute of Immunology, Department of Immunology and Microbiology , Shanghai Jiao Tong University School of Medicine , Shanghai , China.

Insights

Programmed death-1 (PD-1) and its ligand PD-L1 are key regulators of T cell exhaustion. Blocking this pathway with antibodies offers a promising avenue for cancer immunotherapy.

Area of Science:

  • Immunology
  • Oncology
  • Molecular Biology

Background:

  • Programmed death-1 (PD-1) is a crucial T cell checkpoint receptor.
  • Its ligand, programmed death-ligand 1 (PD-L1), inhibits T cell activation upon binding.
  • Elevated PD-L1 expression in tumors facilitates immune escape.

Purpose of the Study:

  • To review the structure and function of the PD-1/PD-L1 signaling pathway.
  • To discuss the application of anti-PD-1/PD-L1 antibodies in cancer immunotherapy.
  • To explore future directions and combination therapies.

Main Methods:

  • Literature review of PD-1 and PD-L1 structure and function.
  • Analysis of PD-1/PD-L1 signaling pathways.
  • Review of current and emerging anti-PD-1/PD-L1 antibody therapies.

Main Results:

  • Detailed review of PD-1 and PD-L1 molecular structures.
  • Explanation of the inhibitory signaling cascade mediated by PD-1/PD-L1.
  • Overview of therapeutic applications of monoclonal antibodies targeting PD-1/PD-L1.

Conclusions:

  • The PD-1/PD-L1 pathway is a significant target for cancer immunotherapy.
  • Anti-PD-1/PD-L1 antibodies represent a rapidly developing therapeutic strategy.
  • Combination therapies hold potential for enhanced efficacy and future curative treatments.

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