Summary:
Background: Sepsis is a serious disease with a high case fatality rate. A variety of changes in the
host immune responsiveness are observed in the pathogenesis of sepsis, ranging from detrimental
hyperinflammation to profound immunoparalysis, i.e. acquired immunodeficiency. The level of
monocyte HLA-DR expression reflects the functional status of monocytes as antigen-presenting
cells and granulocyte CD64 expression is also indicative of infectious inflammation.
Material and Methods: Monocyte HLA-DR expression and granulocyte CD64 expression were measured
in 49 septic patients and 30 healthy controls using flow cytometry focused on three parameters:
positive cell percentage, mean fluorescence intensity and quantitation of antibodies
bound per cell (QuantiBRITE).
Results: The significance of both monocyte HLA-DR expression and granulocyte CD64 expression
in septic patients was confirmed. Monocyte HLA-DR dramatically decreases in septic patients
compared to controls, is one of the prognostic factors and correlates with C-reactive protein. In
contrast, granulocyte CD64 sharply rises in patients with sepsis and correlates with mediators of
systemic inflammation (procalcitonin – PCT), proinflammatory mediators (interleukin-6 – IL-6,
lipopolysaccharide binding protein – LBP) and anti-inflammatory cytokines (interleukin-10 – IL-
10).
Conclusion: Quantitative monocyte HLA-DR expression and granulocyte CD64 expression are useful
indicators in septic patients when considered along with the panel of other markers, monitored
over a period of time and in the context of the clinical course of sepsis.
Key words:
sepsis – immunoparalysis – HLA-DR – CD64 – QuantiBRITE.
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