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TREM-1 expression on neutrophils and monocytes of septic patients: relation to the underlying infection and the
Thekla Poukoulidou1, Aikaterini Spyridaki, Ira Mihailidou
14th Department of Internal Medicine, University of Athens, Medical School, ATTIKON General Hospital, 1 Rimini Str,, 12462 Athens, Greece. tpoukoulidou@hotmail.com
Background:
Current knowledge on the exact ligand causing expression of TREM-1 on neutrophils and monocytes is limited. The present study aimed at the role of underlying infection and of the causative pathogen in the expression of TREM-1 in sepsis.
Methods:
Peripheral venous blood was sampled from 125 patients with sepsis and 88 with severe sepsis/septic shock. The causative pathogen was isolated in 91 patients. Patients were suffering from acute pyelonephritis, community-acquired pneumonia (CAP), intra-abdominal infections (IAIs), primary bacteremia and ventilator-associated pneumonia or hospital-acquired pneumonia (VAP/HAP). Blood monocytes and neutrophils were isolated. Flow cytometry was used to estimate the TREM-1 expression from septic patients.
Results:
Within patients bearing intrabdominal infections, expression of TREM-1 was significantly lower on neutrophils and on monocytes at severe sepsis/shock than at sepsis. That was also the case for severe sepsis/shock developed in the field of VAP/HAP. Among patients who suffered infections by Gram-negative community-acquired pathogens or among patients who suffered polymicrobial infections, expression of TREM-1 on monocytes was significantly lower at the stage of severe sepsis/shock than at the stage of sepsis.
Conclusions:
Decrease of the expression of TREM-1 on the membrane of monocytes and neutrophils upon transition from sepsis to severe sepsis/septic shock depends on the underlying type of infection and the causative pathogen.
Insights
The expression of TREM-1 on immune cells decreases as sepsis progresses to severe sepsis/septic shock, depending on the infection type and pathogen. This finding is crucial for understanding sepsis progression.
Area of Science:
- Immunology
- Infectious Diseases
- Critical Care Medicine
Background:
- Limited understanding of ligands triggering TREM-1 expression on neutrophils and monocytes.
- TREM-1 (Triggering Receptor Expressed on Myeloid cells-1) plays a role in immune responses during infection.
Purpose of the Study:
- To investigate the role of infection type and causative pathogen in TREM-1 expression during sepsis.
- To analyze changes in TREM-1 expression from sepsis to severe sepsis/septic shock.
Main Methods:
- Collected peripheral blood from 125 sepsis and 88 severe sepsis/septic shock patients.
- Identified causative pathogens in 91 patients across various infection types (pyelonephritis, pneumonia, IAIs, bacteremia).
- Utilized flow cytometry to quantify TREM-1 expression on isolated monocytes and neutrophils.
Main Results:
- TREM-1 expression on neutrophils and monocytes was significantly lower in severe sepsis/septic shock compared to sepsis for intra-abdominal infections and VAP/HAP.
- For Gram-negative infections and polymicrobial infections, monocyte TREM-1 expression decreased significantly from sepsis to severe sepsis/septic shock.
Conclusions:
- The reduction in TREM-1 expression during sepsis progression is contingent upon the specific infection and the identified pathogen.
- TREM-1 expression serves as a potential biomarker influenced by infection characteristics in sepsis.
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