Greater T Regulatory Cells in Females Attenuate DOCA-Salt–Induced Increases in Blood Pressure Versus Males. Issue 6 (June 2020)

• Record Type: Journal Article
• Authors: Belanger, Kasey M.; Crislip, G. Ryan; Gillis, Ellen E.; Abdelbary, Mahmoud; Musall, Jacqueline B.; Mohamed, Riyaz; Baban, Babak; Elmarakby, Ahmed; Brands, Michael W.; Sullivan, Jennifer C.
• Is Part Of: Hypertension. Volume 75:Issue 6(2020)
• Publication Date: 2020-06
• Subjects: blood pressure -- cardiovascular disease -- hypertension -- kidney -- inflammation; Hypertension -- Periodicals; Hypertension -- Treatment -- Periodicals; 616.132005
• DOI: 10.1161/HYPERTENSIONAHA.119.14089
• Languages: English
• ISSNs: 0194-911X

Abstract

Abstract : Hypertension is the most common risk factor for cardiovascular disease, causing over 18 million deaths a year. Although the mechanisms controlling blood pressure (BP) in either sex remain largely unknown, T cells play a critical role in the development of hypertension. Further evidence supports a role for the immune system in contributing to sex differences in hypertension. The goal of the current study was to first, determine the impact of sex on the renal T-cell profiles in DOCA-salt hypertensive males and females and second, test the hypothesis that greater numbers of T regulatory cells (Tregs) in females protect against DOCA-salt–induced increases in BP and kidney injury. Male rats displayed greater increases in BP than females following 3 weeks of DOCA-salt treatment, although increases in renal injury were comparable between the sexes. DOCA-salt treatment resulted in an increase in proinflammatory T cells in both sexes; however, females had more anti-inflammatory Tregs than males. Additional male and female DOCA-salt rats were treated with anti-CD25 to decrease Tregs. Decreasing Tregs significantly increased BP only in females, thereby abolishing the sex difference in the BP response to DOCA-salt. This data supports the hypothesis that Tregs protect against the development of hypertension and are particularly important for the control of BP in females. Abstract : Supplemental Digital Content is available in the text.