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Deficiency of Tregs in hypertension-associated left ventricular hypertrophy
Ying Tang1, Li Shen1, Jing-Hui Bao1
1Department of Internal Cardiovascular Medicine, Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Insights
Circulating regulatory T lymphocytes (Tregs) are significantly lower in hypertensive patients with left ventricular hypertrophy (LVH). This decrease is independent of blood pressure and linked to immune factors, suggesting Tregs
Area of Science:
- Immunology
- Cardiology
- Hypertension Research
Background:
- Left ventricular hypertrophy (LVH) is a common complication of hypertension.
- Regulatory T lymphocytes (Tregs) play a crucial role in immune system regulation.
- Abnormal Treg function is implicated in immune disorders and potentially LVH.
Purpose of the Study:
- To investigate the role of circulating Tregs in hypertensive patients with and without LVH.
- To analyze the association between Treg levels, cytokine profiles, and LVH.
- To explore the relationship between Tregs, blood pressure, and demographic factors in hypertension.
Main Methods:
- Blood samples analyzed from 83 hypertensive patients without LVH (EH), 91 with LVH, and 69 controls (CG).
- Quantification of circulating Tregs using flow cytometry.
- Measurement of serum cytokines (IL-10, TGFβ1, IL-6) via enzyme-linked immunosorbent assays.
Main Results:
- Circulating Tregs were significantly lower in hypertensive patients compared to controls, and further reduced in the LVH group versus the EH group.
- Treg levels showed no correlation with blood pressure regulation in EH or LVH patients.
- Tregs negatively correlated with left ventricular mass index (LVMI), creatine kinase, LDL cholesterol, apoprotein B, and hs-CRP.
- Serum IL-10 and TGFβ1 were decreased, while IL-6 was increased in hypertensive patients, particularly in the LVH group.
Conclusions:
- Hypertensive patients with LVH exhibit significantly decreased circulating Tregs, independent of blood pressure.
- Reduced Tregs in LVH are associated with specific inflammatory markers and cardiac remodeling.
- Cytokine profiles (IL-6, IL-10, TGF-β1) are altered in hypertensive LVH, suggesting immune dysregulation's role.
Abstract:
Left ventricular hypertrophy (LVH) is the most common target organ damage in hypertension. Abnormal numbers or functions of CD4+ CD25+ Foxp3+ regulatory T lymphocytes (Tregs) can cause immune disorders, which participates in LVH. This study aimed to explore the role of Tregs in LVH by investigating circulating Tregs and associated cytokine levels in hypertensive patients with or without LVH. Blood samples were collected from 83 hypertensive patients without LVH (essential hypertension group, EH), 91 hypertensive patients with LVH (left ventricular hypertrophy group, LVH), and 69 normotensive controls without LVH (control group, CG). Tregs and cytokines were measured by flow cytometry and enzyme-linked immunosorbent assays. We found that circulating Tregs were significantly lower in hypertensive patients than in CG subjects. It was lower in LVH than in EH patients. No correlation between blood pressure regulation and Tregs was found in EH or LVH patients. Furthermore, Tregs in older females were lower than those in older males among LVH patients. Additionally, serum interleukin-10 (IL-10) and transforming growth factor beta 1 (TGFβ1) decreased in hypertensive patients, and interleukin-6 (IL-6) increased in LVH patients. Tregs were negatively correlated with creatine kinase, low-density lipoprotein cholesterol, apoprotein B, high-sensitivity C-reactive protein, and left ventricular mass index (LVMI) values. In general, our study demonstrates significantly decreased circulating Tregs in hypertensive LVH patients. Decreased circulating Tregs in LVH is independent of blood pressure regulation. IL-6, IL-10, and TGF-β1 are related with LVH in hypertension.
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