Immune checkpoint landscape of human atherosclerosis and influence of cardiometabolic factors

Nat Cardiovasc Res. 2024 Dec;3(12):1482-1502. doi: 10.1038/s44161-024-00563-4. Epub 2024 Nov 29.

Abstract

Immune checkpoint inhibitor (ICI) therapies can increase the risk of cardiovascular events in survivors of cancer by worsening atherosclerosis. Here we map the expression of immune checkpoints (ICs) within human carotid and coronary atherosclerotic plaques, revealing a network of immune cell interactions that ICI treatments can unintentionally target in arteries. We identify a population of mature, regulatory CCR7+FSCN1+ dendritic cells, similar to those described in tumors, as a hub of IC-mediated signaling within plaques. Additionally, we show that type 2 diabetes and lipid-lowering therapies alter immune cell interactions through PD-1, CTLA4, LAG3 and other IC targets in clinical development, impacting plaque inflammation. This comprehensive map of the IC interactome in healthy and cardiometabolic disease states provides a framework for understanding the potential adverse and beneficial impacts of approved and investigational ICIs on atherosclerosis, setting the stage for designing ICI strategies that minimize cardiovascular disease risk in cancer survivors.

MeSH terms

  • Aged
  • Antigens, CD / metabolism
  • Atherosclerosis / immunology
  • Atherosclerosis / metabolism
  • CTLA-4 Antigen / metabolism
  • Cardiometabolic Risk Factors
  • Carotid Artery Diseases / immunology
  • Carotid Artery Diseases / metabolism
  • Coronary Artery Disease* / immunology
  • Coronary Artery Disease* / metabolism
  • Diabetes Mellitus, Type 2 / drug therapy
  • Diabetes Mellitus, Type 2 / immunology
  • Diabetes Mellitus, Type 2 / metabolism
  • Female
  • Humans
  • Immune Checkpoint Inhibitors* / adverse effects
  • Immune Checkpoint Inhibitors* / therapeutic use
  • Immune Checkpoint Proteins / genetics
  • Immune Checkpoint Proteins / metabolism
  • Lymphocyte Activation Gene 3 Protein
  • Male
  • Plaque, Atherosclerotic* / immunology
  • Plaque, Atherosclerotic* / metabolism
  • Plaque, Atherosclerotic* / pathology
  • Programmed Cell Death 1 Receptor / metabolism
  • Signal Transduction

Substances

  • Immune Checkpoint Inhibitors
  • Programmed Cell Death 1 Receptor
  • Lag3 protein, human
  • Lymphocyte Activation Gene 3 Protein
  • Antigens, CD
  • CTLA4 protein, human
  • PDCD1 protein, human
  • Immune Checkpoint Proteins
  • CTLA-4 Antigen