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Enhanced levels of CD154 (CD40 ligand) on platelets in patients with chronic heart failure
Christian Stumpf1, Christoph Lehner, Saeed Eskafi
1Laboratory for Molecular Cardiology, Medical Clinic II, University of Erlangen-Nuremberg, Schwabachanlage 10, Ostfluegel, UG, Erlangen 91054, Germany. ch.stumpf@web.de
Insights
Chronic heart failure (CHF) patients show higher levels of CD154 on platelets, suggesting this immune molecule contributes to inflammation in heart failure. Aspirin did not affect these levels.
Area of Science:
- Cardiology
- Immunology
- Pathophysiology
Background:
- Inflammation is a key factor in chronic heart failure (CHF) pathogenesis.
- Elevated proinflammatory cytokines and immune activation are observed in CHF patients.
- CD154, an immune modulator, is implicated in vascular events like thrombosis and inflammation.
Purpose of the Study:
- To investigate the role of CD154 in the development and progression of CHF.
- To examine CD154 expression on platelets in CHF patients compared to healthy controls.
Main Methods:
- Flow cytometry was used to analyze platelet-bound CD154 and P-selectin expression.
- Fifty CHF patients and 15 healthy controls were studied.
- The influence of aspirin therapy on CD154 expression was assessed.
Main Results:
- CHF patients exhibited significantly higher expression of platelet-bound CD154 and P-selectin compared to controls.
- CD154 expression on platelets positively correlated with CHF severity (NYHA class).
- No significant differences in soluble CD154 or monocyte CD40 expression were found; aspirin did not alter platelet CD154 or P-selectin levels.
Conclusions:
- Elevated CD154 on platelets in CHF patients suggests its involvement in the inflammatory processes of heart failure.
- The CD40-CD154 axis may play a pathogenic role in CHF development and progression.
Background:
Inflammation plays a significant contributory role in the pathogenesis of chronic heart failure (CHF). Previous data have shown enhanced plasma levels of proinflammatory cytokines, i.e. TNF-alpha and IL-6, as well as a persistent immune activation in patients with CHF. Furthermore, the immune modulator CD154 has been receiving increased attention, since it plays a key role in the pathophysiology of multicellular vascular events such as thrombosis, inflammation and atherosclerosis. Since CD154 initiates and maintains the release of proinflammatory cytokines from endothelial cells, its potential role for the development and progression of CHF is of interest.
Methods:
Fifty patients with CHF (aged 66.9+/-12.6 years, mean ejection fraction 22.1+/-9.2%, NYHA II-IV, 39 of ischemic origin, 11 with idiopathic dilated cardiomyopathy) and 15 healthy controls (aged 62.5+/-9.8 years) were examined. Thirty-two patients were taking aspirin (100 mg/day). Blood was drawn from a peripheral vein and immediately fixed with 1% paraformaldehyde, incubated with anti-CD154, anti-P-selectin, and anti-CD61 and thereafter analyzed by flow cytometry.
Results:
Patients with CHF showed significantly enhanced expression of platelet-bound CD154 and P-selectin as compared to controls (CD154: median 35.6 25th percentile: 26.3; 75th percentile: 44.6 vs. 12.8; 25th: 6.8; 75th: 15.6 mean fluorescence intensity [MFI], P<0.001; P-selectin: median 3.2 25th percentile: 1.9; 75th percentile: 5.9 vs. 1.4; 25th: 1.2; 75th: 1.9, MFI, P<0.001). CD154 expression on platelets positively correlated with increasing NYHA-class. In contrast, no significant differences in serum levels of soluble CD154 or CD40 expression on monocytes were detected in the study groups. Antiplatelet-therapy with aspirin did not influence CD154 or P-selectin expression on platelets.
Conclusion:
Our pilot study demonstrates significantly enhanced levels of CD154 on platelets in patients with CHF. This suggests that the CD40-CD154 axis may contribute to the proinflammatory milieu, which exists in CHF and thus may play a pathogenic role in the development and progression of CHF.
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