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      Histopathological evaluation of thrombus in patients presenting with stent thrombosis. A multicenter European study: a report of the prevention of late stent thrombosis by an interdisciplinary global European effort consortium

      research-article
      1 , 2 , 2 , 3 , 3 , 4 , 1 , 2 , 5 , 6 , 7 , 8 , 9 , 6 , 10 , 10 , 11 , 12 , 13 , 11 , 12 , 13 , 14 , 7 , 8 , 15 , 5 , 16 , 16 , 1 , 2 , 1 , 2 , 1 , 2 , 5 , 17 , 6 , 18 , 7 , 8 , 19 , 10 , 1 , 2 , 2 , 3 , * , 1 , 2 , *
      (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab), (Collab)
      European Heart Journal
      Oxford University Press
      Eosinophils, Histopathology, Neutrophils, Neutrophil extracellular traps, Platelets, Stent thrombosis, Thrombus aspiration

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          Abstract

          Background

          Stent thrombosis (ST) is a rare but serious complication following percutaneous coronary intervention. Analysis of thrombus composition from patients undergoing catheter thrombectomy may provide important insights into the pathological processes leading to thrombus formation. We performed a large-scale multicentre study to evaluate thrombus specimens in patients with ST across Europe.

          Methods

          Patients presenting with ST and undergoing thrombus aspiration were eligible for inclusion. Thrombus collection was performed according to a standardized protocol and specimens were analysed histologically at a core laboratory. Serial tissue cross sections were stained with haematoxylin–eosin (H&E), Carstairs and Luna. Immunohistochemistry was performed to identify leukocyte subsets, prothrombotic neutrophil extracellular traps (NETs), erythrocytes, platelets, and fibrinogen.

          Results

          Overall 253 thrombus specimens were analysed; 79 (31.2%) from patients presenting with early ST, 174 (68.8%) from late ST; 79 (31.2%) were from bare metal stents, 166 (65.6%) from drug-eluting stents, 8 (3.2%) were from stents of unknown type. Thrombus specimens displayed heterogeneous morphology with platelet-rich thrombus and fibrin/fibrinogen fragments most abundant; mean platelet coverage was 57% of thrombus area. Leukocyte infiltrations were hallmarks of both early and late ST (early: 2260 ± 1550 per mm 2 vs. late: 2485 ± 1778 per mm 2; P = 0.44); neutrophils represented the most prominent subset (early: 1364 ± 923 per mm 2 vs. late: 1428 ± 1023 per mm 2; P = 0.81). Leukocyte counts were significantly higher compared with a control group of patients with thrombus aspiration in spontaneous myocardial infarction. Neutrophil extracellular traps were observed in 23% of samples. Eosinophils were present in all stent types, with higher numbers in patients with late ST in sirolimus-and everolimus-eluting stents.

          Conclusion

          In a large-scale study of histological thrombus analysis from patients presenting with ST, thrombus specimens displayed heterogeneous morphology. Recruitment of leukocytes, particularly neutrophils, appears to be a hallmark of ST. The presence of NETs supports their pathophysiological relevance. Eosinophil recruitment suggests an allergic component to the process of ST.

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          Most cited references11

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          Reciprocal coupling of coagulation and innate immunity via neutrophil serine proteases.

          Blood neutrophils provide the first line of defense against pathogens but have also been implicated in thrombotic processes. This dual function of neutrophils could reflect an evolutionarily conserved association between blood coagulation and antimicrobial defense, although the molecular determinants and in vivo significance of this association remain unclear. Here we show that major microbicidal effectors of neutrophils, the serine proteases neutrophil elastase and cathepsin G, together with externalized nucleosomes, promote coagulation and intravascular thrombus growth in vivo. The serine proteases and extracellular nucleosomes enhance tissue factor- and factor XII-dependent coagulation in a process involving local proteolysis of the coagulation suppressor tissue factor pathway inhibitor. During systemic infection, activation of coagulation fosters compartmentalization of bacteria in liver microvessels and reduces bacterial invasion into tissue. In the absence of a pathogen challenge, neutrophil-derived serine proteases and nucleosomes can contribute to large-vessel thrombosis, the main trigger of myocardial infarction and stroke. The ability of coagulation to suppress pathogen dissemination indicates that microvessel thrombosis represents a physiological tool of host defense.
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            Thrombosis: tangled up in NETs.

            The contributions by blood cells to pathological venous thrombosis were only recently appreciated. Both platelets and neutrophils are now recognized as crucial for thrombus initiation and progression. Here we review the most recent findings regarding the role of neutrophil extracellular traps (NETs) in thrombosis. We describe the biological process of NET formation (NETosis) and how the extracellular release of DNA and protein components of NETs, such as histones and serine proteases, contributes to coagulation and platelet aggregation. Animal models have unveiled conditions in which NETs form and their relation to thrombogenesis. Genetically engineered mice enable further elucidation of the pathways contributing to NETosis at the molecular level. Peptidylarginine deiminase 4, an enzyme that mediates chromatin decondensation, was identified to regulate both NETosis and pathological thrombosis. A growing body of evidence reveals that NETs also form in human thrombosis and that NET biomarkers in plasma reflect disease activity. The cell biology of NETosis is still being actively characterized and may provide novel insights for the design of specific inhibitory therapeutics. After a review of the relevant literature, we propose new ways to approach thrombolysis and suggest potential prophylactic and therapeutic agents for thrombosis.
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              Coronary neutrophil extracellular trap burden and deoxyribonuclease activity in ST-elevation acute coronary syndrome are predictors of ST-segment resolution and infarct size.

              Mechanisms of coronary occlusion in ST-elevation acute coronary syndrome are poorly understood. We have previously reported that neutrophil (polymorphonuclear cells [PMNs]) accumulation in culprit lesion site (CLS) thrombus is a predictor of cardiovascular outcomes.
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                Author and article information

                Journal
                Eur Heart J
                Eur. Heart J
                eurheartj
                ehj
                European Heart Journal
                Oxford University Press
                0195-668X
                1522-9645
                14 May 2016
                30 August 2015
                30 August 2015
                : 37
                : 19
                : 1538-1549
                Affiliations
                [1 ]Medizinische Klinik und Poliklinik I, Ludwig-Maximilians-Universität , Marchioninistrasse 15, Munich 81377, Germany
                [2 ]DZHK (German Centre for Cardiovascular Research), Partner Site Munich Heart Alliance , Munich, Germany
                [3 ]Deutsches Herzzentrum München, Klinik an der Technische, Universität München , Lazarettstrasse 36, Munich 80636, Germany
                [4 ]CVPath Institute , Gaithersburg, USA
                [5 ]Department of Cardiovascular Sciences, University of Leicester and Leicester NIHR Cardiovascular Biomedical Research Unit, Glenfield Hospital , Leicester LE3 9QP, UK
                [6 ]Department of Cardiology, St. Antonius Hospital , Nieuwegein, The Netherlands
                [7 ]Department of Cardiology, University Hospitals Leuven , Leuven, Belgium
                [8 ]Department of Cardiovascular Sciences, KU Leuven , Leuven, Belgium
                [9 ]Azienda Ospedaliera Papa Giovanni XXIII , Bergamo, Italy
                [10 ]Universitäts-Herzzentrum Freiburg Bad Krozingen , Germany
                [11 ]INSERM, U-1148 , Paris, France
                [12 ]DHU FIRE, Hôpital Bichat, AP-HP , Paris, France
                [13 ]Université Paris-Diderot, Sorbonne Paris-Cité , Paris, France
                [14 ]NHLI, Royal Brompton Hospital, Imperial College , London, UK
                [15 ]Hospital Universitario de La Princesa , Madrid, Spain
                [16 ]Samodzielny Publiczny Zaklad Opieki Zdrowotnej Szpital Uniwersytecki w Krakowie , Krakow, Poland
                [17 ]The Royal Wolverhampton Hospitals NHS Trust, Heart and Lung Centre, New Cross Hospital , Wolverhampton WV10 0QP, UK
                [18 ]Department of Cardiology, Medical Center Alkmaar , Alkmaar, The Netherlands
                [19 ]Antwerp Cardiovascular Institute, ZNA Middelheim , Lindendreef 1, Antwerpen B-2020, Belgium
                Author notes
                [* ]Corresponding author. Tel: +49 89 44007 2371, Fax: +49 89 44007 8870, Email: steffen.massberg@ 123456med.uni-muenchen.de (S.M.); Tel: +49 89 1218 4577, Fax: + 49 89 1218 4083; Email: kastrati@ 123456dhm.mhn.de (A.K.)
                [†]

                An abstract of this work was presented as a late breaking translation science presentation at the European Society of Cardiology Congress 2015 in London, UK.

                [‡]

                These authors contributed equally to this work.

                Article
                ehv419
                10.1093/eurheartj/ehv419
                4872283
                26761950
                744a0b9b-77ac-4967-8a52-9cef6eff3243
                © The Author 2015. Published by Oxford University Press on behalf of the European Society of Cardiology.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 7 July 2015
                : 27 July 2015
                : 6 August 2015
                Funding
                Funded by: European Union Seventh Framework Programme
                Award ID: FP7/2007-2013
                Funded by: HEALTH-F2-2010-260309
                Funded by: PRESTIGE
                Funded by: European Commission http://dx.doi.org/10.13039/501100000780
                Funded by: Seventh Frame Work Programme
                Award ID: 260309
                Funded by: PRESTIGE
                Categories
                ESC FASTTRACK
                ESC Basic and Translational Science Hot Line
                Fast Track

                Cardiovascular Medicine
                eosinophils,histopathology,neutrophils,neutrophil extracellular traps,platelets,stent thrombosis,thrombus aspiration

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