Immune checkpoint landscape of human atherosclerosis and influence of cardiometabolic factors

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<sup>+</sup>FSCN1<sup>+</sup> 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.

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Publication Details

Journal
Nature Cardiovascular Research
Published
2024-11-29
DOI
https://doi.org/10.1038/s44161-024-00563-4
Citations
24
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
Field-Weighted Citation Impact
6.78

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article

Immune checkpoint landscape of human atherosclerosis and influence of cardiometabolic factors

Natalia Eberhardt, Michael Gildea, Kathryn J. Moore, Letizia Amadori et al.
24 citations
Nature Cardiovascular Research
Cancer Immunotherapy and Biomarkers
6.78
article

Immune checkpoint landscape of human atherosclerosis and influence of cardiometabolic factors

Natalia Eberhardt, Michael Gildea, Kathryn J. Moore, Letizia Amadori, José Gabriel Barcia Durán, Swathy Sajja, Navneet Narula, Dayasagar Das, Karishma Rahman, Chiara Giannarelli, Ira J. Goldberg, Burak Cılhoroz, Peter L. Faries, Dawn Fernandez, R. Vanguri, Morgane Gourvest, Edward A. Fisher, Jeffrey S. Berger, Ravneet Kaur, Panagiotis Smyrnis
article en
24 citations

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<sup>+</sup>FSCN1<sup>+</sup> 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.

Nature Cardiovascular ResearchVol. 3(12)
NYU Langone Health (US), New York University (US), Icahn School of Medicine at Mount Sinai (US)
American Heart Association, National Heart, Lung, and Blood Institute
Openalex Percentile: Top 2%
Cancer Immunotherapy and Biomarkers
6.78
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