PSGL-1 Immune Checkpoint Inhibition for CD4+ T Cell Cancer Immunotherapy

  • Front Immunol. 2021 Feb 23:12:636238. doi: 10.3389/fimmu.2021.636238.
Julia M DeRogatis  1 ,  Karla M Viramontes  1 ,  Emily N Neubert  1 ,  Roberto Tinoco  1
Affiliations
  • 1. Department of Molecular Biology and Biochemistry, University of California, Irvine, Irvine, CA, United States.
Abstract

Immune checkpoint inhibition targeting T cells has shown tremendous promise in the treatment of many Cancer types and are now standard therapies for patients. While standard therapies have focused on PD-1 and CTLA-4 blockade, additional immune checkpoints have shown promise in promoting anti-tumor immunity. PSGL-1, primarily known for its role in cellular migration, has also been shown to function as a negative regulator of CD4+ T cells in numerous disease settings including Cancer. PSGL-1 is highly expressed on T cells and can engage numerous ligands that impact signaling pathways, which may modulate CD4+ T cell differentiation and function. PSGL-1 engagement in the tumor microenvironment may promote CD4+ T cell exhaustion pathways that favor tumor growth. Here we highlight that blocking the PSGL-1 pathway on CD4+ T cells may represent a new Cancer therapy approach to eradicate Tumors.

Keywords
CD4+ T cells; PSGL-1; anti-tumor immunity; cancer immunology; immune checkpoints.