Journal article : Review
Immunotherapy for atherosclerosis
- Abstract:
- Cardiovascular disease is the global number one cause of mortality and morbidity. The majority of cardiovascular diseases are caused by atherosclerosis, a lipid-driven, inflammatory disease of the middle- and large-sized arteries. The disease is characterized by the formation of atherosclerotic plaques throughout the arterial tree. Over the years, insights into the pathogenesis of atherosclerosis have shifted from a "lipid-driven" model to a "response-to-injury" perspective and more recently to a "lipid-driven inflammatory disease" viewpoint. We are now aware that a network of multiple immune cell types and subsets of the innate and adaptive immune system inhabit our arteries. Intricate interactions between these immune cell subsets, nonimmune cells, and local environmental substances such as lipids, cell debris, and calcium cause a fluidic balance of proinflammatory and regulatory responses. A dysregulation of this balance toward a proinflammatory milieu drives atherosclerotic disease progression. Although we have acknowledged that atherosclerosis is an inflammatory disease, state-of-the-art treatments are still based on lipid-lowering, antihypertensive, and lifestyle-changing strategies. In the past decade, clinical phase I, II, and III trials targeting the immune system revealed that patients tolerate immunotherapy, show decreased inflammation, and/or have a reduction in cardiovascular endpoints. However, the search for novel immunotherapeutic targets and treatment regimens as well as stratification of patients who would benefit from such treatments to combat atherosclerotic cardiovascular disease is only just beginning. In this review article, we will highlight the newest insights on the different cell subsets and components of the immune system in atherosclerosis and elaborate on current and future immunotherapeutics to treat atherosclerotic cardiovascular disease.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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- Files:
-
-
(Preview, Accepted manuscript, pdf, 7.8MB, Terms of use)
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- Publisher copy:
- 10.1152/physrev.00016.2024
Authors
Contributors
- Publisher:
- American Physiological Society
- Journal:
- Physiological Reviews More from this journal
- Volume:
- 105
- Issue:
- 4
- Pages:
- 2141-2230
- Place of publication:
- United States
- Publication date:
- 2025-06-27
- Acceptance date:
- 2025-05-02
- DOI:
- EISSN:
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1522-1210
- ISSN:
-
0031-9333
- Pmid:
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40397615
- Language:
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English
- Keywords:
- Subtype:
-
Review
- Pubs id:
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2128622
- Local pid:
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pubs:2128622
- Deposit date:
-
2025-10-02
- ARK identifier:
Terms of use
- Copyright holder:
- the American Physiological Society.
- Copyright date:
- 2025
- Rights statement:
- © 2025 the American Physiological Society.
- Notes:
- The author accepted manuscript (AAM) of this paper has been made available under the University of Oxford's Open Access Publications Policy, and a CC BY public copyright licence has been applied.
- Licence:
- CC Attribution (CC BY)
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