Impairment of Circulating CD4+CD25+GARP+ Regulatory T Cells in Patients with Acute Coronary Syndrome

Background: Atherosclerosis (AS) is an inflammatory and immune disease. Regulatory T cells (Tregs) suppress the activation of T cells and have been shown to play a protective role during the pathogenesis of AS. However, specific markers for Tregs are lacking. Recently, glycoprotein A repetitions pre...

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Main Authors: Kai Meng, Wei Zhang, Yucheng Zhong, Xiaobo Mao, Yingzhong Lin, Ying Huang, Mingjian Lang, Yudong Peng, Zhengfeng Zhu, Yuzhou Liu, Xiaoqi Zhao, Kunwu Yu, Bangwei Wu, Qingwei Ji, Qiutang Zeng
Format: Article
Language:English
Published: Cell Physiol Biochem Press GmbH & Co KG 2014-02-01
Series:Cellular Physiology and Biochemistry
Subjects:
Online Access:http://www.karger.com/Article/FullText/358639
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author Kai Meng
Wei Zhang
Yucheng Zhong
Xiaobo Mao
Yingzhong Lin
Ying Huang
Mingjian Lang
Yudong Peng
Zhengfeng Zhu
Yuzhou Liu
Xiaoqi Zhao
Kunwu Yu
Bangwei Wu
Qingwei Ji
Qiutang Zeng
author_facet Kai Meng
Wei Zhang
Yucheng Zhong
Xiaobo Mao
Yingzhong Lin
Ying Huang
Mingjian Lang
Yudong Peng
Zhengfeng Zhu
Yuzhou Liu
Xiaoqi Zhao
Kunwu Yu
Bangwei Wu
Qingwei Ji
Qiutang Zeng
author_sort Kai Meng
collection DOAJ
description Background: Atherosclerosis (AS) is an inflammatory and immune disease. Regulatory T cells (Tregs) suppress the activation of T cells and have been shown to play a protective role during the pathogenesis of AS. However, specific markers for Tregs are lacking. Recently, glycoprotein A repetitions predominant (GARP) was discovered as a specific marker of activated Tregs, and we therefore utilized GARP as a specific surface marker for Tregs in the current study. Methods: To assess whether GARP+ Tregs are downregulated in patients with acute coronary syndrome (ACS), we examined CD4+CD25+GARP+ T cell frequencies as well as their associated cytokines and suppressive function. Additionally, we compared GARP expression to that of FOXP3, which may be more sensitive as a marker of activated Tregs in patients with ACS. Results: Patients with ACS demonstrated a significant decrease in circulating CD4+CD25+GARP+ Tregs. Moreover, the suppressive function of Tregs and levels of related cytokines were also impaired in ACS patients compared to those with stable angina (SA) or normal coronary artery (NCA). Additionally, after TCR stimulation, peripheral blood mononuclear cells (PBMCs) from patients with ACS exhibited a decrease in CD4+CD25+GARP+ Tregs. Conclusions: These fnding indicate that circulating CD4+CD25+GARP+ Tregs are impaired in patients withACS. Thus, targeting GARP may promote the protective function of Tregs in ACS.
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spelling doaj.art-58c7a1cc67b0406c92ddb589e0c077f22022-12-22T00:51:51ZengCell Physiol Biochem Press GmbH & Co KGCellular Physiology and Biochemistry1015-89871421-97782014-02-0133362163210.1159/000358639358639Impairment of Circulating CD4+CD25+GARP+ Regulatory T Cells in Patients with Acute Coronary SyndromeKai MengWei ZhangYucheng ZhongXiaobo MaoYingzhong LinYing HuangMingjian LangYudong PengZhengfeng ZhuYuzhou LiuXiaoqi ZhaoKunwu YuBangwei WuQingwei JiQiutang ZengBackground: Atherosclerosis (AS) is an inflammatory and immune disease. Regulatory T cells (Tregs) suppress the activation of T cells and have been shown to play a protective role during the pathogenesis of AS. However, specific markers for Tregs are lacking. Recently, glycoprotein A repetitions predominant (GARP) was discovered as a specific marker of activated Tregs, and we therefore utilized GARP as a specific surface marker for Tregs in the current study. Methods: To assess whether GARP+ Tregs are downregulated in patients with acute coronary syndrome (ACS), we examined CD4+CD25+GARP+ T cell frequencies as well as their associated cytokines and suppressive function. Additionally, we compared GARP expression to that of FOXP3, which may be more sensitive as a marker of activated Tregs in patients with ACS. Results: Patients with ACS demonstrated a significant decrease in circulating CD4+CD25+GARP+ Tregs. Moreover, the suppressive function of Tregs and levels of related cytokines were also impaired in ACS patients compared to those with stable angina (SA) or normal coronary artery (NCA). Additionally, after TCR stimulation, peripheral blood mononuclear cells (PBMCs) from patients with ACS exhibited a decrease in CD4+CD25+GARP+ Tregs. Conclusions: These fnding indicate that circulating CD4+CD25+GARP+ Tregs are impaired in patients withACS. Thus, targeting GARP may promote the protective function of Tregs in ACS.http://www.karger.com/Article/FullText/358639AtherosclerosisRegulatory T cellsGARPImmune systemAcute coronary syndrome
spellingShingle Kai Meng
Wei Zhang
Yucheng Zhong
Xiaobo Mao
Yingzhong Lin
Ying Huang
Mingjian Lang
Yudong Peng
Zhengfeng Zhu
Yuzhou Liu
Xiaoqi Zhao
Kunwu Yu
Bangwei Wu
Qingwei Ji
Qiutang Zeng
Impairment of Circulating CD4+CD25+GARP+ Regulatory T Cells in Patients with Acute Coronary Syndrome
Cellular Physiology and Biochemistry
Atherosclerosis
Regulatory T cells
GARP
Immune system
Acute coronary syndrome
title Impairment of Circulating CD4+CD25+GARP+ Regulatory T Cells in Patients with Acute Coronary Syndrome
title_full Impairment of Circulating CD4+CD25+GARP+ Regulatory T Cells in Patients with Acute Coronary Syndrome
title_fullStr Impairment of Circulating CD4+CD25+GARP+ Regulatory T Cells in Patients with Acute Coronary Syndrome
title_full_unstemmed Impairment of Circulating CD4+CD25+GARP+ Regulatory T Cells in Patients with Acute Coronary Syndrome
title_short Impairment of Circulating CD4+CD25+GARP+ Regulatory T Cells in Patients with Acute Coronary Syndrome
title_sort impairment of circulating cd4 cd25 garp regulatory t cells in patients with acute coronary syndrome
topic Atherosclerosis
Regulatory T cells
GARP
Immune system
Acute coronary syndrome
url http://www.karger.com/Article/FullText/358639
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