Cytokine production and outcome in MDR versus non-MDR gram-negative bacteraemia and sepsis

Vasileios Karamouzos1, Evangelos J Giamarellos-Bourboulis2, Dimitrios Velissaris3

  • 1Intensive Care Unit, University Hospital of Patras, Patras, Greece.

Abstract

Insights

Multidrug-resistant sepsis patients show a weaker immune response but poorer survival. Carbapenem resistance, male gender, APACHE II score, and angiopoietin-2 levels predict mortality in sepsis.

Area of Science:

  • Critical Care Medicine
  • Infectious Diseases
  • Immunology

Background:

  • Sepsis is a life-threatening condition involving a cytokine storm.
  • The relationship between cytokine levels and pathogen susceptibility in sepsis is debated.
  • Understanding immune response variations in multidrug-resistant (MDR) sepsis is crucial.

Purpose of the Study:

  • To investigate immune responses in MDR and non-MDR sepsis patients by measuring cytokine levels.
  • To compare patient outcomes based on MDR status.
  • To identify predictors of mortality in sepsis patients.

Main Methods:

  • 128 sepsis patients in the ICU were enrolled.
  • Plasma levels of angiopoietin-2 (Ang-2), IL-6, IL-10, TNF-α, and sTREM-1 were measured.
  • Epidemiological and ICU data, including APACHE II scores, were collected.

Main Results:

  • Tumor necrosis factor-α (TNF-α) levels were higher in non-MDR sepsis patients (p=0.017).
  • Pro-inflammatory cytokines increased with higher APACHE II scores.
  • Multidrug-resistant (MDR) sepsis patients had significantly lower 28-day survival (p=0.008).
  • Predictors of mortality included carbapenem resistance (OR 5.38), male gender (OR 2.76), APACHE II score (OR 1.126), and Ang-2 (OR 1.025).

Conclusions:

  • Multidrug-resistant (MDR) pathogens may elicit a weaker immune response (lower TNF-α) but do not improve survival.
  • Increased angiopoietin-2 (Ang-2) levels, higher APACHE II scores, and carbapenem resistance are significant predictors of mortality in sepsis.
  • Sepsis outcomes are multifactorial, influenced by pathogen resistance and host immune response.

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