Decreased Helios Expression in Regulatory T Cells in Acute Coronary Syndrome

Dis Markers. 2017:2017:7909407. doi: 10.1155/2017/7909407. Epub 2017 Nov 12.

Abstract

Regulatory T cells (Tregs) play an essential role in acute coronary syndrome (ACS). However, there is debate about which Treg subsets are truly critical to ACS. Helios, a transcription factor, was recently reported to be a bona fide marker for natural Tregs or activated Tregs with a suppression function, but little is known about its role in ACS. We therefore examined Helios+ Tregs in patients with ACS, patients with stable angina, and control subjects. 73 patients with ACS, 30 patients with stable angina, and 48 control subjects were enrolled. The frequencies and estimated absolute numbers of different Treg subsets in peripheral blood were measured by flow cytometry. Plasma cytokine level was measured by ELISA. The mRNA expression of Foxp3 and Helios in purified CD4+ T cells was determined by RT-PCR. Helios+ Tregs was decreased significantly in patients with ACS. The frequency and estimated absolute numbers of CD4+Foxp3+Helios+ Tregs were negatively correlated with IL-6 and positively correlated with circulating level of TGF-beta1 and HDL-C. The mRNA expression of Foxp3 and Helios was decreased in CD4+ T cells from patients with ACS. In summary, Helios+ Tregs was downregulated in patients with ACS and may play a role in ACS.

MeSH terms

  • Acute Coronary Syndrome / blood*
  • Acute Coronary Syndrome / genetics
  • Acute Coronary Syndrome / metabolism
  • Angina, Stable / blood*
  • Angina, Stable / genetics
  • Angina, Stable / metabolism
  • Biomarkers / blood
  • CD4-Positive T-Lymphocytes / metabolism
  • Female
  • Forkhead Transcription Factors / genetics
  • Forkhead Transcription Factors / metabolism
  • Humans
  • Ikaros Transcription Factor / blood*
  • Ikaros Transcription Factor / genetics
  • Ikaros Transcription Factor / metabolism
  • Male
  • Middle Aged

Substances

  • Biomarkers
  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • IKZF2 protein, human
  • Ikaros Transcription Factor