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Increased circulating soluble CD14 is associated with high mortality in gram-negative septic shock
R Landmann1, W Zimmerli, S Sansano
1Department of Research, University Hospital, Basel, Switzerland.
The Journal of Infectious Diseases
|March 1, 1995
Summary
Soluble CD14 (sCD14) levels are higher in gram-negative septic shock patients and correlate with mortality. The sCD14 level, not its form, predicts outcomes in this critical condition.
Area of Science:
- Immunology
- Critical Care Medicine
- Biochemistry
Background:
- Soluble glycoprotein sCD14 binds lipopolysaccharide (LPS), activating endothelial cells.
- This interaction is potentially crucial in the pathogenesis of gram-negative sepsis.
- Endothelial cell activation by LPS is a key event in septic shock.
Purpose of the Study:
- To investigate serum sCD14 levels in patients with gram-negative septic shock.
- To determine the prognostic value of sCD14 levels and its isoforms in septic shock.
- To compare sCD14 concentrations between septic shock patients and healthy controls.
Main Methods:
- Serum sCD14 was quantified using ELISA and Western blotting.
- Analysis included 54 patients with gram-negative septic shock and 26 healthy controls.
- Isoforms of sCD14 were identified in monocyte cultures and patient sera.
Main Results:
- Septic shock patients exhibited significantly higher serum sCD14 concentrations than controls (median, 3.23 vs. 2.48 µg/mL; P = .002).
- Elevated sCD14 levels were strongly associated with increased mortality (median, 4.2 µg/mL in nonsurvivors vs. 2.8 µg/mL in survivors; P = .001).
- While controls had the 49-kDa form, septic patients showed either 49- or 55-kDa forms; high sCD14 levels correlated with the 55-kDa form.
Conclusions:
- Serum sCD14 levels are significantly elevated in gram-negative septic shock.
- The concentration of sCD14, rather than its specific biochemical isoform, serves as a valuable prognostic indicator.
- Higher sCD14 levels are directly associated with increased mortality risk in gram-negative septic shock patients.