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.
Purpose:
IL-17-producing T cells have been implicated in the inflammatory milieu of chronic heart failure (CHF), which implies a dismal prognosis in affected patients. The aim of this study was to evaluate the impact of cardiac resynchronization therapy (CRT) on the frequency and functional activity of Th17 and Tc17 cells, as well as, on IL-17 mRNA expression in patients with CHF.
Methods:
Twenty-eight patients with CHF, analyzed before CRT (T0) and 6 months later (T6), and 15 healthy controls (HC) were enrolled in this study. Circulating Th17 and Tc17 cells were evaluated by flow cytometry. The quantification of IL-17A mRNA expression was performed by real-time PCR.
Results:
Circulating Tc17 cells tended to be higher in CHF patients submitted to CRT than in HC (0.92% (0.24-3.32) versus 0.60% (0.09-3.68), although not reaching statistical significance. The frequency of Tc17 cells in CHF patients significantly decreases after CRT reaching levels similar to those of HC (0.92% (0.24-3.32) at T0 versus 0.56% (0.21-4.20) at T6, P < 0.05), mainly due to responders to CRT. Additionally, the expression of IL-17 mRNA was detected in a few number of responder patients at T0 (27%) and only detected in one responder at T6 (7%). Conversely, in non-responders, the proportion of patients exhibiting IL-17 mRNA expression increases from baseline (17%) to T6 (42%). No significant differences were observed in Th17 cells between HC, CHF patients in T0 and patients in T6.
Conclusion:
The inflammatory response mediated by circulating IL-17 producing cells seems to be suppressed by CRT, particularly in responders.
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