Abstract

IntroductionOur aim was to define early changes of lymphocytes and of NK cells in severe sepsis and to correlate them with serum levels of soluble triggering receptor expressed on myeloid cells-1 (sTREM-1).MethodsBlood was sampled from 49 patients with proven highly suspected infection by Gram-negative pathogens, within 12 hours of the advent of severe sepsis, and was also sampled from six healthy volunteers. White blood cells were targeted with monoclonal antibodies and were analyzed by flow cytometry. The concentrations of sTREM-1 were estimated by ELISA.ResultsThe presence of CD3/CD4 cells was significantly lower (P < 0.0001) and that of NK cells significantly higher among patients with sepsis compared with controls (P = 0.011). The proportions (median ± standard error) of ANNEXIN-V/CD4/CD3-positive cells, of ANNEXIN-V/CD8/CD3-positive cells and of ANNEXIN-V/CD14-positive cells of the patient population were 7.41 ± 2.26%, 7.69 ± 3.42% and 1.96 ± 4.22%, respectively. Patients with NK cells >20% survived longer compared with those patients with NK cells ≤20% (P = 0.041), and patients with sTREM-1 concentrations >180 pg/ml survived longer compared with those patients with sTREM-1 concentrations ≤180 pg/ml (P = 0.042). A negative correlation was found between the percentages of ANNEXIN-V/CD4/CD3-positive cells and of CD3/CD4 cells (rs = -0.305, P = 0.049), and a positive correlation was found between the serum sTREM-1 concentration and the percentage of NK cells (rs = +0.395, P = 0.014). NK cells isolated from two healthy volunteers released sTREM-1 upon triggering with endotoxins.ConclusionEarly severe sepsis is characterized by CD4-lymphopenia and increased NK cells, providing a survival benefit for the septic patient at percentages >20%. The survival benefit resulting from elevated NK cells might be connected to elevated serum levels of sTREM-1.

Highlights

  • Our aim was to define early changes of lymphocytes and of NK cells in severe sepsis and to correlate them with serum levels of soluble triggering receptor expressed on myeloid cells-1

  • Patients with NK cells >20% survived longer compared with those patients with NK cells ≤20% (P = 0.041), and patients with soluble triggering receptor expressed on myeloid cells-1 (sTREM-1) concentrations >180 pg/ml survived longer compared with those patients with sTREM-1 concentrations ≤180 pg/ml (P = 0.042)

  • A negative correlation was found between the percentages of ANNEXIN-V/CD4/CD3positive cells and of CD3/CD4 cells, and a positive correlation was found between the serum sTREM-1 concentration and the percentage of NK cells

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Summary

Introduction

Our aim was to define early changes of lymphocytes and of NK cells in severe sepsis and to correlate them with serum levels of soluble triggering receptor expressed on myeloid cells-1 (sTREM-1). Human studies in patients with sepsis have shown considerable changes in the subpopulations of lymphocytes [1], and of those lymphocytes participating in adaptive immunity. Sparse data of either animal or human studies implicate a crucial role of new counterparts of the innate immune system in the pathogenesis of sepsis. These data comprise NK cells that are a subpopulation of lymphocytes behaving as cells of the innate immune system [2], as well as neutrophils and monocytes expressing the triggering receptor expressed on myeloid cells-1 receptor on their cell membranes in the event of human sepsis [3]. The soluble form of this receptor, namely soluble triggering receptor expressed on myeloid cells-1 (sTREM-1), is proposed to act as an anti-inflammatory mediator and to contribute to the transition from sepsis to septic shock [4,5]

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