Alarmin S100A8/S100A9 as a biomarker for molecular imaging of local inflammatory activity

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作者
Thomas Vogl
Michel Eisenblätter
Tom Völler
Stefanie Zenker
Sven Hermann
Peter van Lent
Andreas Faust
Christiane Geyer
Beatrix Petersen
Kirsten Roebrock
Michael Schäfers
Christoph Bremer
Johannes Roth
机构
[1] Institute of Immunology,Division of Imaging Sciences and Biomedical Engineering
[2] University of Münster,Department of Clinical Radiology
[3] Interdisciplinary Centre for Clinical Research,Department of Rheumatology
[4] University of Münster,Department of Radiology
[5] King’s College London,undefined
[6] University of Münster,undefined
[7] European Institute for Molecular Imaging,undefined
[8] University of Münster,undefined
[9] Radboud University Medical Centre,undefined
[10] Cluster of Excellence EXC 1003 ‘Cells in Motion - CiM’,undefined
[11] University of Münster,undefined
[12] St Franziskus Hospital Münster,undefined
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摘要
Inflammation has a key role in the pathogenesis of various human diseases. The early detection, localization and monitoring of inflammation are crucial for tailoring individual therapies. However, reliable biomarkers to detect local inflammatory activities and to predict disease outcome are still missing. Alarmins, which are locally released during cellular stress, are early amplifiers of inflammation. Here, using optical molecular imaging, we demonstrate that the alarmin S100A8/S100A9 serves as a sensitive local and systemic marker for the detection of even sub-clinical disease activity in inflammatory and immunological processes like irritative and allergic contact dermatitis. In a model of collagen-induced arthritis, we use S100A8/S100A9 imaging to predict the development of disease activity. Furthermore, S100A8/S100A9 can act as a very early and sensitive biomarker in experimental leishmaniasis for phagocyte activation linked to an effective Th1-response. In conclusion, the alarmin S100A8/S100A9 is a valuable and sensitive molecular target for novel imaging approaches to monitor clinically relevant inflammatory disorders on a molecular level.
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