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Published Online First: 8 August 2007. doi:10.1136/hrt.2007.117259
Heart 2008;94:770-776
Copyright © 2008 BMJ Publishing Group Ltd & British Cardiovascular Society

ORIGINAL ARTICLES

Molecular biology and genetics

Monocyte toll-like receptor 2 and 4 responses and expression following percutaneous coronary intervention: association with lesion stenosis and fractional flow reserve

D Versteeg1, I E Hoefer1, A H Schoneveld1,2, D P V de Kleijn1,2, E Busser1, C Strijder1, M Emons1, P R Stella1, P A Doevendans1,2, G Pasterkamp1

1 Experimental Cardiology Laboratory, Department of Cardiology, University Medical Centre, Utrecht, The Netherlands
2 Interuniversity Cardiology Institute of the Netherlands (ICIN), Utrecht, The Netherlands

Dr G Pasterkamp, Experimental Cardiology Laboratory (Room G02.523), University Medical Centre, Utrecht, Heidelberglaan 100, PO Box 85500, 3508 GA, Utrecht, The Netherlands; g.pasterkamp{at}umcutrecht.nl

Background: Toll-like receptors (TLRs) are key players in innate immunity and are causally related to arterial occlusive disease and arterial remodelling. The release of proinflammatory cytokines following TLR ligand binding is increased in patients with unstable angina.

Objective: To examine the effect of a percutaneous coronary intervention (PCI) on TLR2 and TLR4 response and expression.

Methods: In 70 PCI patients, blood samples were gathered after sheath insertion and 2 hours after the catheterisation. TLR2 and TLR4 expression on, and tumour necrosis factor {alpha} (TNF{alpha}) levels in, monocytes were measured with flow cytometry. Whole blood was stimulated overnight with the TLR2 ligand Pam3Cys and the TLR4 ligand lipopolysaccharide. TNF{alpha} was determined in the stimulated samples and considered to be a measure of the TLR response. Baseline TLR expression and response were studied in relation to angiographic luminal stenosis and fractional flow reserve (FFR) measurement.

Results: A significant relation was found between TLR response and the angiographic percentage diameter stenosis, number of diseased vessels and FFR outcome. Furthermore, 2 hours after PCI a significant decrease in TLR2 and TLR4 response (p<0.001) and TLR2 and TLR4 expression (p = 0.001 and p = 0.068, respectively) was seen.

Conclusion: TLR response is positively associated with percentage diameter stenosis, multivessel disease and FFR outcome. Systemic TLR2 and TLR4 response and expression decrease after PCI. These results suggests that the TLR signalling pathway encompasses a potential biomarker for myocardial ischaemia in stable coronary artery disease.


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This article has been cited by other articles:

  • Pasterkamp, G., Daemen, M. (2008). Circulating cells: the biofactory for markers of atherosclerotic disease. Eur Heart J 29: 2701-2702 [Full Text]  

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