Differentiating sepsis from non-infectious systemic inflammation based on microvesicle-bacteria aggregation

Nanoscale. 2015 Aug 28;7(32):13511-20. doi: 10.1039/c5nr01851j. Epub 2015 Jul 23.

Abstract

Sepsis is a severe medical condition and a leading cause of hospital mortality. Prompt diagnosis and early treatment has a significant, positive impact on patient outcome. However, sepsis is not always easy to diagnose, especially in critically ill patients. Here, we present a conceptionally new approach for the rapid diagnostic differentiation of sepsis from non-septic intensive care unit patients. Using advanced microscopy and spectroscopy techniques, we measure infection-specific changes in the activity of nano-sized cell-derived microvesicles to bind bacteria. We report on the use of a point-of-care-compatible microfluidic chip to measure microvesicle-bacteria aggregation and demonstrate rapid (≤1.5 hour) and reliable diagnostic differentiation of bacterial infection from non-infectious inflammation in a double-blind pilot study. Our study demonstrates the potential of microvesicle activities for sepsis diagnosis and introduces microvesicle-bacteria aggregation as a potentially useful parameter for making early clinical management decisions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacteria / isolation & purification*
  • Cell Aggregation
  • Cell-Derived Microparticles / microbiology*
  • Diagnosis, Differential
  • Disease Models, Animal
  • Humans
  • Microfluidic Analytical Techniques
  • Neutrophils / microbiology
  • Rats
  • Sepsis / blood
  • Sepsis / diagnosis*
  • Sepsis / microbiology
  • Systemic Inflammatory Response Syndrome / blood
  • Systemic Inflammatory Response Syndrome / diagnosis*
  • Systemic Inflammatory Response Syndrome / microbiology