Overview of multifunctional Tregs in cardiovascular disease: From insights into cellular functions to clinical implications.
Vipin KumarMegumi NarisawaXian Wu ChengPublished in: FASEB journal : official publication of the Federation of American Societies for Experimental Biology (2024)
Regulatory T cells (Tregs) are crucial in regulating T-cell-mediated immune responses. Numerous studies have shown that dysfunction or decreased numbers of Tregs may be involved in inflammatory cardiovascular diseases (CVDs) such as atherosclerosis, hypertension, myocardial infarction, myocarditis, cardiomyopathy, valvular heart diseases, heart failure, and abdominal aortic aneurysm. Tregs can help to ameliorate CVDs by suppressing excessive inflammation through various mechanisms, including inhibition of T cells and B cells, inhibition of macrophage-induced inflammation, inhibition of dendritic cells and foam cell formation, and induction of anti-inflammatory macrophages. Enhancing or restoring the immunosuppressive activity of Tregs may thus serve as a fundamental immunotherapy to treat hypertension and CVDs. However, the precise molecular mechanisms underlying the Tregs-induced protection against hypertension and CVDs remain to be investigated. This review focuses on recent advances in our understanding of Tregs subsets and function in CVDs. In addition, we discuss promising strategies for using Tregs through various pharmacological approaches to treat hypertension and CVDs.
Keyphrases
- cardiovascular disease
- heart failure
- dendritic cells
- blood pressure
- regulatory t cells
- oxidative stress
- immune response
- abdominal aortic aneurysm
- diabetic rats
- atrial fibrillation
- anti inflammatory
- type diabetes
- left ventricular
- adipose tissue
- drug delivery
- single cell
- stem cells
- coronary artery disease
- physical activity
- drug induced
- cardiovascular risk factors
- toll like receptor
- weight gain
- peripheral blood
- single molecule
- atomic force microscopy