Extracellular heat shock protein 60 (Hsp60) levels in children with septic shock

D S Wheeler1, P Lahni, K Odoms

  • 1Division of Critical Care Medicine, Cincinnati Children's Hospital Medical Center, Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, 45229-3039, USA. derek.wheeler@cchmc.org

Insights

Extracellular heat shock protein 60 (Hsp60) levels were significantly elevated in children with septic shock. This finding suggests Hsp60 may play a role in pediatric sepsis pathogenesis.

Area of Science:

  • Immunology
  • Pediatrics
  • Biochemistry

Background:

  • Extracellular heat shock protein 60 (Hsp60) is implicated in modulating innate immune responses.
  • Understanding biomarkers for pediatric sepsis is crucial for timely diagnosis and treatment.

Purpose of the Study:

  • To investigate plasma extracellular Hsp60 levels in children diagnosed with septic shock.
  • To compare Hsp60 levels between septic shock patients, critically ill non-septic children, and healthy controls.

Main Methods:

  • Plasma samples were collected from three groups: children with septic shock (n=63), critically ill children without septic shock (n=10), and healthy controls (n=24).
  • Extracellular Hsp60 concentrations were quantified using enzyme-linked immunosorbent assay (ELISA).
  • Statistical analysis employed the Kruskal-Wallis one-way ANOVA to determine significant differences between groups.

Main Results:

  • Children with septic shock exhibited significantly higher plasma Hsp60 levels (median, 16.7 ng/mL) compared to both critically ill children without septic shock (median, 0 ng/mL) and healthy controls (median, 0 ng/mL).
  • The observed differences between the septic shock group and the other two groups were statistically significant (p <0.001).

Conclusions:

  • Plasma extracellular Hsp60 levels are markedly elevated in pediatric patients experiencing septic shock.
  • Elevated extracellular Hsp60 may serve as a potential biomarker and contribute to the pathogenesis of sepsis in children.
Abstract

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