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Updated: Jun 22, 2025

An Adoptive Transfer Model of Rheumatoid Arthritis in Mice
Published on: June 6, 2025
Crosstalk between Inflammation and Atherosclerosis in Rheumatoid Arthritis and Systemic Lupus Erythematosus: Is There
Marta Chiara Sircana1, Gian Luca Erre1, Floriana Castagna1
1Department of Medical, Surgical and Pharmacology, University of Sassari, 07100 Sassari, Italy.
Insights
Inflammation drives atherosclerosis in rheumatoid arthritis and systemic lupus erythematosus, explaining early cardiovascular disease beyond traditional risk factors. Chronic inflammation
Area of Science:
- Immunology
- Cardiovascular Medicine
- Rheumatology
Background:
- Cardiovascular disease (CVD) is a major cause of death in rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE).
- Traditional CVD risk factors do not fully account for the high incidence of early-onset CVD in these autoimmune diseases.
- Atherosclerosis pathogenesis is increasingly understood as an inflammation-centric process.
Purpose of the Study:
- To review the pathogenesis of atherosclerosis in RA and SLE.
- To highlight RA and SLE as models for chronic inflammation's impact on cardiovascular health.
- To explore immune system involvement in atherosclerosis within these diseases.
Main Methods:
- Review of current literature on atherosclerosis in RA and SLE.
- Examination of the roles of inflammasomes, immune cells (neutrophils, macrophages, lymphocytes), and inflammatory mediators.
- Investigation of autoantigens (e.g., oxidized LDL) and autoantibodies (e.g., anti-beta2-glycoprotein I) in disease progression.
Main Results:
- Chronic inflammation, mediated by immune cells and cytokines, is central to atherosclerosis in RA and SLE.
- Specific immune pathways and autoantibodies contribute significantly to cardiovascular risk.
- The inflammatory milieu in RA and SLE accelerates atherosclerotic plaque development.
Conclusions:
- Atherosclerosis in RA and SLE is driven by chronic systemic inflammation.
- Targeting inflammatory pathways offers potential therapeutic strategies for cardiovascular risk reduction in these patients.
- Understanding immune-mediated mechanisms is crucial for managing CVD in autoimmune diseases.
Abstract:
Cardiovascular disease is the leading cause of morbidity and mortality in patients with rheumatoid arthritis and systemic lupus erythematosus. Traditional cardiovascular risk factors, although present in lupus and rheumatoid arthritis, do not explain such a high burden of early cardiovascular disease in the context of these systemic connective tissue diseases. Over the past few years, our understanding of the pathophysiology of atherosclerosis has changed from it being a lipid-centric to an inflammation-centric process. In this review, we examine the pathogenesis of atherosclerosis in systemic lupus erythematosus and rheumatoid arthritis, the two most common systemic connective tissue diseases, and consider them as emblematic models of the effect of chronic inflammation on the human body. We explore the roles of the inflammasome, cells of the innate and acquired immune system, neutrophils, macrophages, lymphocytes, chemokines and soluble pro-inflammatory cytokines in rheumatoid arthritis and systemic lupus erythematosus, and the roles of certain autoantigens and autoantibodies, such as oxidized low-density lipoprotein and beta2-glycoprotein, which may play a pathogenetic role in atherosclerosis progression.
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