Increased Th17 cells in coronary artery disease are associated with neutrophilic inflammation

Scand Cardiovasc J. 2011 Feb;45(1):54-61. doi: 10.3109/14017431.2010.491123. Epub 2011 Jan 12.

Abstract

Objective: Atherosclerosis is a progressive disease characterized by a series of inflammatory responses in the large and medium arteries. Th17 cells, a distinct T cell lineage which has recently been identified, have a proinflammatory role and are implicated in many inflammatory conditions in humans and mice. The present study was designed to assess whether Th17 cells are associated with human coronary atherosclerosis.

Design: Flow cytometry was used to examine Th17 cell frequencies in patients with coronary atherosclerosis and in healthy individuals. ELISA and real-time RT-PCR were performed to investigate circulating interleukin (IL)-17 (the signature cytokine of Th17 cells) and IL-8 (the cytokine induced by IL-17) protein and mRNA levels.

Results: Significantly increased Th17 cell frequencies are observed in patients with coronary artery disease compared to healthy controls. The protein and mRNA levels of IL-17 and IL-8 are also significantly elevated in patients with atherosclerosis compared to healthy volunteers. Furthermore, mRNA levels of IL-17 and IL-8 are correlated with each other and with peripheral neutrophil counts.

Conclusions: Our findings indicate that Th17 cells and their signature cytokine are involved in the process of atherogenesis. These data suggest that Th17 cells link T cell activity with neutrophilic inflammation in atherosclerosis.

MeSH terms

  • Adult
  • Atherosclerosis / blood
  • Atherosclerosis / etiology
  • Atherosclerosis / pathology
  • Case-Control Studies
  • Cell Count
  • Coronary Artery Disease / blood
  • Coronary Artery Disease / pathology*
  • Female
  • Humans
  • Inflammation / etiology
  • Inflammation / pathology*
  • Interleukin-17 / blood
  • Interleukin-8 / blood
  • Male
  • Middle Aged
  • Neutrophils / pathology*
  • RNA, Messenger / blood
  • Th17 Cells / metabolism
  • Th17 Cells / pathology*

Substances

  • Interleukin-17
  • Interleukin-8
  • RNA, Messenger