Immune Profiling Reveals Decreases in Circulating Regulatory and Exhausted T Cells in Human Hypertension

被引:18
作者
Alexander, Matthew R. [1 ,2 ,3 ,4 ,9 ]
Dale, Bethany L. [4 ,5 ]
Smart, Charles D.
Elijovich, Fernando [1 ]
Wogsland, Cara E. [6 ,7 ]
Lima, Sierra M. [8 ]
Irish, Jonathan M. [3 ,8 ]
Madhur, Meena S. [1 ,2 ,3 ,4 ]
机构
[1] Vanderbilt Univ, Med Ctr, Div Clin Pharmacol, Dept Med, Nashville, TN 37235 USA
[2] Vanderbilt Univ, Med Ctr, Div Cardiovasc Med, Dept Med, Nashville, TN USA
[3] Vanderbilt Inst Infect Immunol Flammat, Nashville, TN USA
[4] Vanderbilt Univ, Dept Mol Physiol & Biophys, Nashville, TN USA
[5] Pirche, Berlin, Germany
[6] Vanderbilt Univ, Med Ctr, Dept Pathol Microbiol & Immunol, Nashville, TN USA
[7] KinN Therapeut, Bergen, Norway
[8] Vanderbilt Univ, Sch Med, Dept Cell & Dev Biol, Nashville, TN USA
[9] Vanderbilt Univ, Med Ctr, Div Clin Pharmacol, Dept Med, 2215 Garland Ave, Nash, TN 37232 USA
基金
美国国家卫生研究院;
关键词
hypertension; inflammation; immunity; lymphocytes; mass cytometry; MASS CYTOMETRY; BLOOD-PRESSURE; DIFFERENTIATION; INFLAMMATION; EXPRESSION; CHEMOKINE; RESPONSES; EFFECTOR; CCR10; MOUSE;
D O I
10.1016/j.jacbts.2022.09.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Evidence from nonhuman animal models demonstrates an important role for immune cells in hypertension, but immune cell changes in human hypertension are less clear. Using mass cytometry, we demonstrate novel and selective reductions in CCR10+ regulatory T cells (Tregs) and PD-1+CD57-CD8+ memory T cells. RNA sequencing reveals that CCR10+ Tregs exhibit gene expression changes consistent with enhanced immuno-suppressive function. In addition, CITE-Seq demonstrates that PD-1+CD57-CD8+ memory T cells exhibit features of T-cell exhaustion. Taken together, these results provide novel evidence for decreases in anti-inflammatory and/or hypofunctional T-cell populations that may contribute to enhanced inflammation in human hypertension. (J Am Coll Cardiol Basic Trans Science 2023;8:319-336) (c) 2023 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:319 / 336
页数:18
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