Treg/Th17 balance in stable CAD patients with different stages of coronary atherosclerosis

Atherosclerosis. 2015 Jan;238(1):17-21. doi: 10.1016/j.atherosclerosis.2014.10.088. Epub 2014 Nov 20.

Abstract

Objective. Immune processes play a significant role in atherosclerosis plaque progression. Regulatory T cells and T helpers 17 were shown to possess anti- and pro-atherogenic activity, respectively. We aimed to investigate the balance of circulating Treg and Th17 in stable angina patients with different stages of coronary atherosclerosis. Methods. Treg, Th17 and Th1 cell frequencies were studied in 117 patients via direct immunofluorescence staining and flow cytometry. Group 1 had intact coronary arteries. Group 2 and Group 3 had undergone previous coronary stenting; in Group 2 no coronary atherosclerosis progression was found, in Group 3 patients had disease progression in non-invaded coronary arteries. Group 4 had severe coronary atherosclerosis. Results. The frequencies of CD4+CD25highCD127low, CD4+foxp3+, and CD4+IL10 + T cells were decreased, and CD4+IL17 + T cells frequencies were increased in group 4 vs. 1. Treg/Th17 ratios were declined in groups 3 and 4 vs. groups 1 and 2. IL-10 level was lower while hsCRP and sCD25 levels were higher in group 4 vs. 1. Conclusion. We assume that the imbalance in pro- and anti-inflammatory/atherogenic lymphocyte subpopulations is associated with atherosclerosis progression.

Keywords: Coronary artery disease; Regulatory T cells; T helpers 17.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Atherosclerosis / immunology*
  • Atherosclerosis / pathology
  • Coronary Artery Disease / immunology*
  • Coronary Artery Disease / pathology
  • Coronary Vessels / pathology
  • Cytokines / metabolism
  • Disease Progression
  • Female
  • Flow Cytometry
  • Forkhead Transcription Factors / metabolism
  • Humans
  • Immunosuppressive Agents / therapeutic use
  • Inflammation / pathology
  • Interleukin-10 / metabolism
  • Interleukin-17 / metabolism
  • Interleukin-2 Receptor alpha Subunit / metabolism
  • Interleukin-7 Receptor alpha Subunit / metabolism
  • Male
  • Microscopy, Fluorescence
  • Middle Aged
  • T-Lymphocytes, Regulatory / cytology*
  • Th17 Cells / cytology*

Substances

  • Cytokines
  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • Immunosuppressive Agents
  • Interleukin-17
  • Interleukin-2 Receptor alpha Subunit
  • Interleukin-7 Receptor alpha Subunit
  • Interleukin-10