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Updated: Feb 9, 2026

In Silico Clinical Trials for Cardiovascular Disease
Published on: May 27, 2022
Myeloid cell contributions to cardiovascular health and disease
1Center for Systems Biology and Cardiovascular Research Center, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA. mnahrendorf@mgh.harvard.edu.
Insights
New cell tracing and sequencing technologies reveal insights into leukocyte behavior, highlighting inflammatory cells like macrophages as key targets for cardiovascular disease therapies. Understanding these cells is crucial for developing precision immunotherapies.
Area of Science:
- Immunology
- Cardiovascular Biology
- Genomics
Background:
- Leukocyte behavior is increasingly understood through cell tracing and sequencing.
- Inflammatory cells, particularly monocyte-derived macrophages, are emerging as drug targets for cardiovascular diseases like atherosclerosis, myocardial infarction, and heart failure.
- Harmful macrophage subsets in arteries and the heart, altered production, and epigenetic memory in myeloid progenitors are key findings.
Purpose of the Study:
- To review recent advances in understanding leukocyte subsets, sources, and functions in cardiovascular disease.
- To explore the potential of targeting monocytes and macrophages for precision cardiovascular therapeutics.
- To discuss how integrated clinical and preclinical data advance the concept of cardiovascular immunotherapy.
Main Methods:
- Review of recent clinical and preclinical data.
- Analysis of cell tracing and sequencing technologies.
- Integration of findings across cardiovascular, immune, and other organ systems.
Main Results:
- Identification of specific harmful arterial and cardiac macrophage subsets.
- Understanding of altered and potentially clonal production of these cells in hematopoietic organs.
- Recognition of epigenetically entrained memories in myeloid progenitors and macrophages relevant to cardiovascular disease.
Conclusions:
- Intricate understanding of monocyte and macrophage subsets, sources, and functions is essential for developing precision therapeutics.
- These insights are critical for preserving protective innate immunity while treating cardiovascular disease.
- Cardiovascular immunotherapy is becoming a tangible therapeutic strategy based on current research.
Abstract:
Recent advances in cell tracing and sequencing technologies have expanded our knowledge on leukocyte behavior. As a consequence, inflammatory cells, such as monocyte-derived macrophages, and their actions and products are increasingly being considered as potential drug targets for treatment of atherosclerosis, myocardial infarction and heart failure. Particularly promising developments are the identification of harmful arterial and cardiac macrophage subsets, the cells' altered, sometimes even clonal production in hematopoietic organs, and epigenetically entrained memories of myeloid progenitors and macrophages in the setting of cardiovascular disease. Given the roles of monocytes and macrophages in host defense, intricately understanding the involved cellular subsets, sources and functions is essential for the design of precision therapeutics that preserve protective innate immunity. Here I review how new clinical and preclinical data, often linking the cardiovascular, immune and other organ systems, propel conceptual advances to a point where cardiovascular immunotherapy appears within reach.
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