• Ioanna Dimopoulou, Aimilia Pelekanou, Irini Mavrou, Athina Savva, Marinella Tzanela, Antigone Kotsaki, Matina Kardara, Stylianos E Orfanos, Anastasia Kotanidou, and Evangelos J Giamarellos-Bourboulis.
• 2nd Department of Critical Care Medicine, University of Athens, Medical School, Greece.
• J Crit Care. 2012 Jun 1;27(3):294-300.

PurposeTo define early kinetics of soluble triggering receptor expressed on myeloid cells-1 (sTREM-1) and of TREM-1 monocyte gene expression in critically ill patients with sepsis.MethodsBlood was sampled at regular time intervals from 105 patients with sepsis. Concentrations of tumour necrosis factor α (TNFα), interleukin (IL)-6, IL-8 and IL-10 and IL-12p70 and sTREM-1 were measured by an enzyme immunoassay. Blood mononuclear cells were isolated on day 0 from 20 patients and 10 healthy volunteers; RNA was extracted and gene expression of TREM-1 and TNFα were assessed by reverse transcriptase polymerase chain reaction.ResultsEarly serum concentrations of sTREM-1 were greater among patients with severe sepsis/shock than among patients with sepsis; those of TNFα, IL-6, IL-8 and IL-10 were pronounced among patients with septic shock. Gene transcripts of TNFα were lower among patients with severe sepsis/shock than among patients with sepsis; that was not the case for TREM-1. Early serum levels of sTREM-1 greater than 180 pg/mL were predictors of shorter duration of mechanical ventilation.ConclusionsAlthough serum levels of sTREM-1 are increased early upon advent of severe sepsis/shock, gene expression of TREM-1 on monocytes in severe sepsis/shock is not increased. These findings add considerably to our knowledge on the pathophysiology of sepsis.Copyright © 2012 Elsevier Inc. All rights reserved.

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