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Impaired circulating CD4+ LAP+ regulatory T cells in patients with acute coronary syndrome and its mechanistic study Zhu ZF; Meng K; Zhong YC; Qi L; Mao XB; Yu KW; Zhang W; Zhu PF; Ren ZP; Wu BW; Ji QW; Wang X; Zeng QTPLoS One 2014[]; 9 (2): e88775OBJECTIVE: CD4(+) latency-associated peptide (LAP)(+) regulatory T cells (Tregs) are a newly discovered T cell subset in humans and the role of these cells in patients with acute coronary syndrome (ACS) has not been explored. We designed to investigate whether circulating frequency and function of CD4(+)LAP(+) Tregs are defective in ACS. METHODS: One hundred eleven ACS patients (acute myocardial infarction and unstable angina) and 117 control patients were enrolled in the study. The control patients consisted of chronic stable angina (CSA) and chest pain syndrome (CPS). The frequencies of circulating CD4(+)LAP(+) Tregs and the expression of the transmembrane protein glycoprotein-A repetitions predominant (GARP) on CD4(+) T cells were determined by flow cytometry. The function of CD4(+)LAP(+) Tregs was detected using thymidine uptake. Serum interleukin-10 (IL-10) and transforming growth factor-beta protein (TGF-beta) levels were detected using ELISA and expression of GARP mRNA in peripheral blood mononuclear cells (PBMCs) was measured by real time-polymerase chain reaction. RESULTS: We found ACS patients had a significantly lower frequency of circulating CD4(+)LAP(+) Tregs, and the function of these cells was reduced compared to controls. The expression of GARP in CD4(+) T cells and the serum levels of TGF-beta in ACS patients were lower than those of control patients. The serum levels of IL-10 were similar between the two cohorts. CONCLUSIONS: A novel regulatory T cell subset, defined as CD4(+)LAP(+) T cells is defective in ACS patients.|Acute Coronary Syndrome/*blood/genetics/*immunology[MESH]|Angina, Stable/blood/immunology[MESH]|Chest Pain/blood/immunology[MESH]|Female[MESH]|Gene Expression Regulation[MESH]|Humans[MESH]|Male[MESH]|Membrane Proteins/genetics[MESH]|Middle Aged[MESH]|RNA, Messenger/genetics/metabolism[MESH]|T-Lymphocytes, Regulatory/*cytology[MESH]|Transforming Growth Factor beta1/blood[MESH] |
