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Published on: January 22, 2019
T-Cell Molecular Modulation Responses in Atherosclerosis Anergy
Bahram Pakzad1, Elham Rajae2, Saeid Shahrabi3
1Internal Medicine Department, Isfahan University of Medical Sciences, Isfahan, Iran.
This review explores how T cells influence inflammation in atherosclerosis, a major cardiovascular disease. Targeting T cell responses and microRNAs offers potential therapeutic strategies to manage atherosclerosis complications.
Area of Science:
- Immunology
- Cardiovascular Research
- Molecular Biology
Background:
- Atherosclerosis remains a leading cause of death globally, associated with cardiovascular diseases.
- The role of the immune system, particularly adaptive T cell responses, in atherosclerotic plaque inflammation is increasingly recognized.
Purpose of the Study:
- To review the involvement of T cells in atherosclerosis-mediated inflammation.
- To explore potential therapeutic strategies for ameliorating atherosclerosis complications through immunomodulation.
Main Methods:
- Review of current literature on T cell subsets, cytokines, and microRNAs in atherosclerosis.
- Analysis of growth factor/receptor axes and their impact on the atherosclerotic inflammatory cycle.
Main Results:
- T-lymphocyte subsets, microRNAs (miRs), and growth factor/receptor interactions significantly affect the inflammatory cycle of atherosclerosis.
- Manipulation of miRNA expression and growth factor receptors shows promise as diagnostic biomarkers for inducing anergy and blocking disease progression.
Conclusions:
- T cell-mediated immune responses play a critical role in the pathogenesis of atherosclerosis.
- Targeting T cell responses, microRNAs, and specific growth factor pathways presents viable therapeutic avenues for managing atherosclerosis and its complications.
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