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Effector T cell chemokine IP-10 predicts cardiac recovery and clinical outcomes post-myocardial infarction

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Effector T cell chemokine IP-10 predicts cardiac recovery and clinical outcomes post-myocardial infarction. / Sopova, Kateryna; Tual-Chalot, Simon; Mueller-Hennessen, Matthias et al.
In: Frontiers in Immunology, Vol. 14, 1177467, 22.06.2023.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Sopova, K, Tual-Chalot, S, Mueller-Hennessen, M, Vlachogiannis, NI, Georgiopoulos, G, Biener, M, Sachse, M, Turchinovich, A, Polycarpou-Schwarz, M, Spray, L, Maneta, E, Bennaceur, K, Mohammad, A, Richardson, GD, Gatsiou, A, Langer, HF, Frey, N, Stamatelopoulos, K, Heineke, J, Duerschmied, D, Giannitsis, E, Spyridopoulos, I & Stellos, K 2023, 'Effector T cell chemokine IP-10 predicts cardiac recovery and clinical outcomes post-myocardial infarction', Frontiers in Immunology, vol. 14, 1177467. https://doi.org/10.3389/fimmu.2023.1177467

APA

Sopova, K., Tual-Chalot, S., Mueller-Hennessen, M., Vlachogiannis, N. I., Georgiopoulos, G., Biener, M., Sachse, M., Turchinovich, A., Polycarpou-Schwarz, M., Spray, L., Maneta, E., Bennaceur, K., Mohammad, A., Richardson, G. D., Gatsiou, A., Langer, H. F., Frey, N., Stamatelopoulos, K., Heineke, J., ... Stellos, K. (2023). Effector T cell chemokine IP-10 predicts cardiac recovery and clinical outcomes post-myocardial infarction. Frontiers in Immunology, 14, Article 1177467. https://doi.org/10.3389/fimmu.2023.1177467

Vancouver

Sopova K, Tual-Chalot S, Mueller-Hennessen M, Vlachogiannis NI, Georgiopoulos G, Biener M et al. Effector T cell chemokine IP-10 predicts cardiac recovery and clinical outcomes post-myocardial infarction. Frontiers in Immunology. 2023 Jun 22;14:1177467. doi: 10.3389/fimmu.2023.1177467

Author

Sopova, Kateryna ; Tual-Chalot, Simon ; Mueller-Hennessen, Matthias et al. / Effector T cell chemokine IP-10 predicts cardiac recovery and clinical outcomes post-myocardial infarction. In: Frontiers in Immunology. 2023 ; Vol. 14.

Bibtex

@article{41b97877ec484179bf4991e227e335af,
title = "Effector T cell chemokine IP-10 predicts cardiac recovery and clinical outcomes post-myocardial infarction",
abstract = "BACKGROUND AND AIMS: Preclinical data suggest that activation of the adaptive immune system is critical for myocardial repair processes in acute myocardial infarction. The aim of the present study was to determine the clinical value of baseline effector T cell chemokine IP-10 blood levels in the acute phase of ST-segment elevation myocardial infarction (STEMI) for the prediction of the left ventricular function changes and cardiovascular outcomes after STEMI.METHODS: Serum IP-10 levels were retrospectively quantified in two independent cohorts of STEMI patients undergoing primary percutaneous coronary intervention.RESULTS: We report a biphasic response of the effector T cell trafficking chemokine IP-10 characterized by an initial increase of its serum levels in the acute phase of STEMI followed by a rapid reduction at 90min post reperfusion. Patients at the highest IP-10 tertile presented also with more CD4 effector memory T cells (CD4 TEM cells), but not other T cell subtypes, in blood. In the Newcastle cohort (n=47), patients in the highest IP-10 tertile or CD4 TEM cells at admission exhibited an improved cardiac systolic function 12 weeks after STEMI compared to patients in the lowest IP-10 tertile. In the Heidelberg cohort (n=331), STEMI patients were followed for a median of 540 days for major adverse cardiovascular events (MACE). Patients presenting with higher serum IP-10 levels at admission had a lower risk for MACE after adjustment for traditional risk factors, CRP and high-sensitivity troponin-T levels (highest vs. rest quarters: HR [95% CI]=0.420 [0.218-0.808]).CONCLUSION: Increased serum levels of IP-10 in the acute phase of STEMI predict a better recovery in cardiac systolic function and less adverse events in patients after STEMI.",
keywords = "Humans, Chemokine CXCL10, Heart, Myocardial Infarction, Retrospective Studies, ST Elevation Myocardial Infarction/therapy",
author = "Kateryna Sopova and Simon Tual-Chalot and Matthias Mueller-Hennessen and Vlachogiannis, {Nikolaos I} and Georgios Georgiopoulos and Moritz Biener and Marco Sachse and Andrey Turchinovich and Maria Polycarpou-Schwarz and Luke Spray and Eleni Maneta and Karim Bennaceur and Ashfaq Mohammad and Richardson, {Gavin David} and Aikaterini Gatsiou and Langer, {Harald F} and Norbert Frey and Kimon Stamatelopoulos and Joerg Heineke and Daniel Duerschmied and Evangelos Giannitsis and Ioakim Spyridopoulos and Konstantinos Stellos",
note = "Copyright {\textcopyright} 2023 Sopova, Tual-Chalot, Mueller-Hennessen, Vlachogiannis, Georgiopoulos, Biener, Sachse, Turchinovich, Polycarpou-Schwarz, Spray, Maneta, Bennaceur, Mohammad, Richardson, Gatsiou, Langer, Frey, Stamatelopoulos, Heineke, Duerschmied, Giannitsis, Spyridopoulos and Stellos.",
year = "2023",
month = jun,
day = "22",
doi = "10.3389/fimmu.2023.1177467",
language = "English",
volume = "14",
journal = "Frontiers in Immunology",
issn = "1664-3224",
publisher = "Frontiers Media S.A.",

}

RIS

TY - JOUR

T1 - Effector T cell chemokine IP-10 predicts cardiac recovery and clinical outcomes post-myocardial infarction

AU - Sopova, Kateryna

AU - Tual-Chalot, Simon

AU - Mueller-Hennessen, Matthias

AU - Vlachogiannis, Nikolaos I

AU - Georgiopoulos, Georgios

AU - Biener, Moritz

AU - Sachse, Marco

AU - Turchinovich, Andrey

AU - Polycarpou-Schwarz, Maria

AU - Spray, Luke

AU - Maneta, Eleni

AU - Bennaceur, Karim

AU - Mohammad, Ashfaq

AU - Richardson, Gavin David

AU - Gatsiou, Aikaterini

AU - Langer, Harald F

AU - Frey, Norbert

AU - Stamatelopoulos, Kimon

AU - Heineke, Joerg

AU - Duerschmied, Daniel

AU - Giannitsis, Evangelos

AU - Spyridopoulos, Ioakim

AU - Stellos, Konstantinos

N1 - Copyright © 2023 Sopova, Tual-Chalot, Mueller-Hennessen, Vlachogiannis, Georgiopoulos, Biener, Sachse, Turchinovich, Polycarpou-Schwarz, Spray, Maneta, Bennaceur, Mohammad, Richardson, Gatsiou, Langer, Frey, Stamatelopoulos, Heineke, Duerschmied, Giannitsis, Spyridopoulos and Stellos.

PY - 2023/6/22

Y1 - 2023/6/22

N2 - BACKGROUND AND AIMS: Preclinical data suggest that activation of the adaptive immune system is critical for myocardial repair processes in acute myocardial infarction. The aim of the present study was to determine the clinical value of baseline effector T cell chemokine IP-10 blood levels in the acute phase of ST-segment elevation myocardial infarction (STEMI) for the prediction of the left ventricular function changes and cardiovascular outcomes after STEMI.METHODS: Serum IP-10 levels were retrospectively quantified in two independent cohorts of STEMI patients undergoing primary percutaneous coronary intervention.RESULTS: We report a biphasic response of the effector T cell trafficking chemokine IP-10 characterized by an initial increase of its serum levels in the acute phase of STEMI followed by a rapid reduction at 90min post reperfusion. Patients at the highest IP-10 tertile presented also with more CD4 effector memory T cells (CD4 TEM cells), but not other T cell subtypes, in blood. In the Newcastle cohort (n=47), patients in the highest IP-10 tertile or CD4 TEM cells at admission exhibited an improved cardiac systolic function 12 weeks after STEMI compared to patients in the lowest IP-10 tertile. In the Heidelberg cohort (n=331), STEMI patients were followed for a median of 540 days for major adverse cardiovascular events (MACE). Patients presenting with higher serum IP-10 levels at admission had a lower risk for MACE after adjustment for traditional risk factors, CRP and high-sensitivity troponin-T levels (highest vs. rest quarters: HR [95% CI]=0.420 [0.218-0.808]).CONCLUSION: Increased serum levels of IP-10 in the acute phase of STEMI predict a better recovery in cardiac systolic function and less adverse events in patients after STEMI.

AB - BACKGROUND AND AIMS: Preclinical data suggest that activation of the adaptive immune system is critical for myocardial repair processes in acute myocardial infarction. The aim of the present study was to determine the clinical value of baseline effector T cell chemokine IP-10 blood levels in the acute phase of ST-segment elevation myocardial infarction (STEMI) for the prediction of the left ventricular function changes and cardiovascular outcomes after STEMI.METHODS: Serum IP-10 levels were retrospectively quantified in two independent cohorts of STEMI patients undergoing primary percutaneous coronary intervention.RESULTS: We report a biphasic response of the effector T cell trafficking chemokine IP-10 characterized by an initial increase of its serum levels in the acute phase of STEMI followed by a rapid reduction at 90min post reperfusion. Patients at the highest IP-10 tertile presented also with more CD4 effector memory T cells (CD4 TEM cells), but not other T cell subtypes, in blood. In the Newcastle cohort (n=47), patients in the highest IP-10 tertile or CD4 TEM cells at admission exhibited an improved cardiac systolic function 12 weeks after STEMI compared to patients in the lowest IP-10 tertile. In the Heidelberg cohort (n=331), STEMI patients were followed for a median of 540 days for major adverse cardiovascular events (MACE). Patients presenting with higher serum IP-10 levels at admission had a lower risk for MACE after adjustment for traditional risk factors, CRP and high-sensitivity troponin-T levels (highest vs. rest quarters: HR [95% CI]=0.420 [0.218-0.808]).CONCLUSION: Increased serum levels of IP-10 in the acute phase of STEMI predict a better recovery in cardiac systolic function and less adverse events in patients after STEMI.

KW - Humans

KW - Chemokine CXCL10

KW - Heart

KW - Myocardial Infarction

KW - Retrospective Studies

KW - ST Elevation Myocardial Infarction/therapy

U2 - 10.3389/fimmu.2023.1177467

DO - 10.3389/fimmu.2023.1177467

M3 - Journal article

C2 - 37426649

VL - 14

JO - Frontiers in Immunology

JF - Frontiers in Immunology

SN - 1664-3224

M1 - 1177467

ER -