Impact of cardiac resynchronization therapy on circulating IL-17 producing cells in patients with advanced heart

Sílvia Martins1,2, Tiago Carvalheiro3, Paula Laranjeira2,4

  • 1CICS-UBI - Centro de Investigação em Ciências da Saúde, Universidade da Beira Interior, Covilhã, Portugal.

Insights

Cardiac resynchronization therapy (CRT) reduced the frequency of IL-17-producing T cells in chronic heart failure (CHF) patients, particularly in responders. This suggests CRT may suppress the inflammatory response associated with CHF.

Area of Science:

  • Immunology
  • Cardiology
  • Molecular Biology

Background:

  • Interleukin-17 (IL-17)-producing T cells are linked to poor prognosis in chronic heart failure (CHF).
  • Understanding the role of these cells and the impact of treatments like cardiac resynchronization therapy (CRT) is crucial for managing CHF.

Purpose of the Study:

  • To investigate the effect of CRT on the frequency and function of T helper 17 (Th17) and T cytotoxic 17 (Tc17) cells.
  • To assess changes in IL-17 messenger RNA (mRNA) expression following CRT in CHF patients.

Main Methods:

  • Flow cytometry was used to quantify circulating Th17 and Tc17 cells in 28 CHF patients before (T0) and 6 months after (T6) CRT, and in 15 healthy controls (HC).
  • Real-time polymerase chain reaction (PCR) was employed to measure IL-17A mRNA expression.

Main Results:

  • Tc17 cell frequency decreased significantly in CHF patients after CRT (T0 vs. T6, P < 0.05), returning to levels similar to HC.
  • IL-17 mRNA expression was detected in a subset of responders at T0 and T6, but increased in non-responders at T6.
  • No significant changes in Th17 cell frequency were observed across groups.

Conclusions:

  • CRT appears to suppress the inflammatory response mediated by IL-17-producing cells in CHF patients.
  • The suppression is particularly evident in patients who respond to CRT.
Abstract

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