Harnessing CD8 T cell responses using PD-1-IL-2 combination therapy

Trends Cancer. 2024 Apr;10(4):332-346. doi: 10.1016/j.trecan.2023.11.008. Epub 2023 Dec 20.

Abstract

There is considerable interest in developing more effective programmed cell death (PD)-1 combination therapies against cancer. One major obstacle to these efforts is a dysfunctional/exhausted state of CD8 T cells, which PD-1 monotherapy is not able to overcome. Recent studies have highlighted that PD-1+ T cell factor (TCF)-1+ stem-like CD8 T cells are not fate locked into the exhaustion program and their differentiation trajectory can be changed by interleukin (IL)-2 signals. Modifying the CD8 T cell exhaustion program and generating better effectors from stem-like CD8 T cells by IL-2 form the fundamental immunological basis for combining IL-2 with PD-1 therapy. Many versions of IL-2-based products are being tested and each product should be carefully evaluated for its ability to modulate dysfunctional states of anti-tumor CD8 T cells.

Keywords: IL-2; PD-1; T cell exhaustion; cancer; chronic infection; immunotherapy.

Publication types

  • Review

MeSH terms

  • CD8-Positive T-Lymphocytes
  • Cell Differentiation
  • Humans
  • Interleukin-2 / metabolism
  • Interleukin-2 / pharmacology
  • Interleukin-2 / therapeutic use
  • Neoplasms* / drug therapy
  • Neoplasms* / metabolism
  • Programmed Cell Death 1 Receptor* / metabolism

Substances

  • Programmed Cell Death 1 Receptor
  • Interleukin-2