J Pediatr Intensive Care 2014; 03(01): 009-016
DOI: 10.3233/PIC-14083
Georg Thieme Verlag KG Stuttgart – New York

The extracellular stress response to pediatric cardiopulmonary bypass

Derek S. Wheeler
a   Divisions of Critical Care Medicine and Cardiology, Cincinnati Children's Hospital Medical Center, Departments of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA
,
Michael T. Bigham
b   Division of Critical Care Medicine, Akron Children's Hospital, Akron, OH, USA
,
Patrick M. Lahni
a   Divisions of Critical Care Medicine and Cardiology, Cincinnati Children's Hospital Medical Center, Departments of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA
,
John S. Giuliano
c   Division of Critical Care Medicine, Yale-New Haven Children's Hospital, Yale School of Medicine, New Haven, CT, USA
,
David P. Nelson
a   Divisions of Critical Care Medicine and Cardiology, Cincinnati Children's Hospital Medical Center, Departments of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA
,
Peter B. Manning
d   Division of Pediatric Cardiothoracic Surgery, St. Louis Children's Hospital, Washington University School of Medicine, St. Louis, MO, USA
,
Hector R. Wong
a   Divisions of Critical Care Medicine and Cardiology, Cincinnati Children's Hospital Medical Center, Departments of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA
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16. Mai 2014

25. Juni 2014

Publikationsdatum:
28. Juli 2015 (online)

Abstract

The heat shock response, also frequently referred to as the stress response, is an ancient, highly conserved, endogenous cellular defense mechanism characterized by the rapid upregulation of a specific class of proteins known collectively as heat shock proteins, or stress proteins. The 70 kDa family of heat shock proteins are highly inducible and have been shown to possess important immunomodulatory effects in both the intracellular and extracellular compartments. In the current prospective translational study, we measured extracellular (i.e. plasma) levels of heat shock protein 72 (Hsp72) in 49 children undergoing cardiopulmonary bypass (CPB) for either palliation or repair of congenital heart disease. There was a significant and transient increase (less than 24 h) in extracellular Hsp72 levels following CPB. Extracellular Hsp72 levels significantly correlated with levels of the pro-inflammatory cytokines interleukin (IL)-6 and IL-8, as well as the anti-inflammatory cytokine, IL-10. In addition, plasma Hsp72 levels correlated with troponin-I levels, a marker of myocardial injury. Increased extracellular Hsp72 levels at 6 h following CPB were independently associated with increased length of stay in the cardiac intensive care unit. Importantly, the source of extracellular Hsp72 does not appear to be cardiomyocytes. However, the mechanism of release and clinical relevance of the increase in extracellular Hsp72 need to be further delineated.