Functional Expression of Programmed Death-Ligand 1 (B7-H1) by Immune Cells and Tumor Cells

Rachel M Gibbons Johnson1, Haidong Dong2,3

  • 1Biology Discipline, University of Minnesota Morris, Morris, MN, United States.

Frontiers in Immunology
|August 30, 2017
PubMed

Insights

The programmed death-1 (PD-1) and programmed death-ligand 1 (PD-L1) pathway is crucial in cancer immunotherapy. This review explores PD-L1

Area of Science:

  • Oncology
  • Immunology
  • Cancer Immunotherapy

Background:

  • The PD-1/PD-L1 pathway is a key target in cancer treatment, with approved checkpoint blockade therapies.
  • Tumor cell PD-L1 expression is a known factor influencing T cell responses, but its role is not fully understood.
  • Some patients respond to PD-L1/PD-1 blockade despite lacking PD-L1 expression on tumor cells, suggesting other factors are involved.

Purpose of the Study:

  • To review the functions of PD-L1 expressed by immune cells in CD8+ T cell responses.
  • To examine the role of tumor cell PD-L1 in regulating antitumor CD8+ T cell activity.
  • To highlight the importance of non-malignant cell PD-L1 in antitumor immunity.

Main Methods:

  • Literature review of studies on PD-1/PD-L1 pathway in cancer immunology.
  • Analysis of the impact of PD-L1 on immune cells, specifically CD8+ T cells.
  • Examination of PD-L1 expression in both tumor cells and non-malignant cells.

Main Results:

  • PD-L1 on tumor cells influences CD8+ T cell responses.
  • PD-L1 on immune cells plays a role in T cell priming, contraction, and memory differentiation.
  • PD-L1 expression by non-malignant cells may contribute to antitumor immunity.

Conclusions:

  • Understanding PD-L1 expression on both tumor and immune cells is critical for optimizing cancer immunotherapy.
  • PD-L1 on immune cells significantly impacts CD8+ T cell dynamics and antitumor responses.
  • Further research into the multifaceted roles of PD-L1 is essential for advancing checkpoint blockade therapies.

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