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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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Publisher copy:
10.1152/physrev.00016.2024

Authors

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Institution:
University of Oxford
Division:
MSD
Department:
NDORMS
Sub department:
Kennedy Institute for Rheumatology
Role:
Author
ORCID:
0000-0002-6716-2528

Contributors


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Funder identifier:
https://ror.org/01czwga19


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:
1522-1210
ISSN:
0031-9333
Pmid:
40397615


Language:
English
Keywords:
Subtype:
Review
Pubs id:
2128622
Local pid:
pubs:2128622
Deposit date:
2025-10-02
ARK identifier:

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