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A Human Ex Vivo Atherosclerotic Plaque Model to Study Lesion Biology
Published on: May 6, 2014
Inflammatory Basis of Atherosclerosis: Modulation by Sex Hormones
Suzanne A Nasser1, Elham A Afify2, Firas Kobeissy3
1Department of Pharmacology and Therapeutics, Faculty of Pharmacy, Beirut Arab University, P.O. Box 11-5020, Beirut, Lebanon.
Insights
Sex hormones significantly influence vascular inflammation, a key factor in atherosclerosis-related cardiovascular diseases (CVDs). Understanding these interactions may lead to sex-specific treatments for CVDs.
Area of Science:
- Cardiovascular Science
- Immunology
- Endocrinology
Background:
- Atherosclerosis-related cardiovascular diseases (CVDs) are the leading global cause of death.
- Vascular inflammation, involving immune cells and lipid mediators, plays a critical role in atherosclerosis.
- Sex differences in CVD prevalence suggest a role for sex hormones.
Purpose of the Study:
- To review vascular inflammation in atherosclerosis, focusing on sex hormone modulation.
- To highlight cellular and molecular pathways in sex hormone-immune system interactions.
- To speculate on sex-related efficacy of immunotherapies for vascular inflammation.
Main Methods:
- Literature review of animal and human studies.
- Analysis of cellular and molecular signaling pathways.
- Discussion of sex hormone receptors in vascular and immune cells.
Main Results:
- Sex hormones are implicated in driving immune responses relevant to CVD.
- Sex hormone receptors are present in key vascular and immune cells.
- Cellular communication between sex hormones and vascular/immune cells contributes to vascular inflammation.
Conclusions:
- Vascular inflammation is a causal factor in atherosclerosis-related CVDs, modulated by sex hormones.
- Understanding sex hormone-immune interactions is crucial for managing atherosclerosis.
- Potential for sex-based immunotherapies to mitigate vascular inflammation exists.
Abstract:
Atherosclerosis-related cardiovascular diseases (CVDs) are the leading cause of death globally. Several lines of evidence are supportive of the contributory role of vascular inflammation in atherosclerosis. Diverse immune cell types, including monocytes/macrophages, T-cells and neutrophils, as well as specialized proresolving lipid mediators, have been successfully characterized as key players in vascular inflammation. The increased prevalence of atherosclerotic CVD in men in comparison to age-matched premenopausal women and the abolition of sex differences in prevalence during menopause strongly suggest a pivotal role of sex hormones in the development of CVD. Indeed, many animal and human studies conclusively implicate sex hormones as a crucial component in driving the immune response. This is further corroborated by the effective identification of sex hormone receptors in vascular endothelial cells, vascular smooth muscle cells and immune cells. Collectively, these findings suggest a cellular communication between sex hormones and vascular or immune cells underlying the vascular inflammation in atherosclerosis. The aim of this review is to provide an overview of vascular inflammation as a causal cue underlying atherosclerotic CVDs within the context of the modulatory effects of sex hormones. Moreover, the cellular and molecular signaling pathways underlying the sex hormones- immune system interactions as potential culprits for vascular inflammation are highlighted with detailed and critical discussion. Finally, the review concludes by speculations on the potential sex-related efficacy of currently available immunotherapies in mitigating vascular inflammation. Conceivably, a deeper understanding of the immunoregulatory influence of sex hormones on vascular inflammation-mediated atherosclerosis permits sex-based management of atherosclerosis-related CVDs.
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