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Sex Differences in the Immune System in Relation to Hypertension and Vascular Disease
Kevin D Comeau1, Brandon G Shokoples1, Ernesto L Schiffrin2
1Hypertension and Vascular Research Unit, Lady Davis Institute for Medical Research, McGill University, Montréal, Québec, Canada.
Insights
Sex differences in hypertension are linked to immune responses. Male hypertension involves pro-inflammatory T cells, while females are protected by anti-inflammatory T regulatory cells until menopause.
Area of Science:
- Cardiovascular Science
- Immunology
- Endocrinology
Background:
- Hypertension is a major global risk factor for cardiovascular disease and mortality.
- Despite extensive research, blood pressure control remains challenging for many patients.
- Sex disparities exist in hypertension prevalence, with higher rates in young men and post-menopausal women.
Purpose of the Study:
- To investigate the role of sex and immune system differences in hypertension.
- To explore how sex hormones influence immune cell function in hypertension.
- To identify potential new therapeutic targets by understanding sex-specific mechanisms.
Main Methods:
- Analysis of male and female animal models of hypertension.
- Examination of T-cell subsets (e.g., TH17 cells) and their cytokine production (e.g., IL-17, IL-10).
- Assessment of immune cell infiltration in renal tissue.
Main Results:
- Hypertensive male animals exhibited increased pro-inflammatory TH17 cells and renal immune cell infiltration.
- Premenopausal female animals showed protection, with a preference for anti-inflammatory T regulatory cells and IL-10 production.
- Menopause appeared to diminish this protective effect in females.
Conclusions:
- Immune system responses, particularly T-cell profiles, differ significantly between sexes in hypertension.
- Sex hormones likely modulate these immune responses, influencing hypertension development and progression.
- Understanding these sex-specific immune mechanisms may lead to novel hypertension treatments.
Abstract:
Hypertension is the leading risk factor for cardiovascular disease and mortality worldwide. Despite intensive research into the mechanisms underlying the development of hypertension, it remains difficult to control blood pressure in a large proportion of patients. Young men have a higher prevalence of hypertension compared with age-matched women, and this holds true until approximately the fifth decade of life. Following the onset of menopause, the incidence of hypertension among women begins to surpass that of men. The immune system has been demonstrated to play a role in the pathophysiology of hypertension, and biological sex and sex hormones can affect the function of innate and adaptive immune cell populations. Recent studies in male and female animal models of hypertension have begun to unravel the relationship among sex, immunity, and hypertension. Hypertensive male animals show a bias toward proinflammatory T-cell subsets, including interleukin (IL) 17-producing TH17 cells, and increased renal infiltration of T cells and inflammatory macrophages. Conversely, premenopausal female animals are largely protected from hypertension, and have a predilection for anti-inflammatory T regulatory cells and production of anti-inflammatory cytokines, such as IL-10. Menopause abrogates female protection from hypertension, which may be due to changes among anti-inflammatory T regulatory cell populations. Since development of novel treatments for hypertension has plateaued, determining the role of sex in the pathophysiology of hypertension may open new therapeutic avenues for both men and women.
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