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Updated: Sep 15, 2025

Isolation and Characterization of Neutrophils with Anti-Tumor Properties
Published on: June 19, 2015
Exploratory Study of CD10low Polymorphonuclear Leukocytes Preceding and Correlating With Postsurgical Inflammation
Timo Michael Westermann1, Joe Sendas1, Alexander Sebastian Koller1
1Institute of Clinical and Experimental Trauma Immunology, University Hospital Ulm, Ulm, Germany.
Immature CD10-low polymorphonuclear leukocytes (PMNs) show potential as early biomarkers for postsurgical inflammation. Their numbers rise before established markers, aiding in rapid risk assessment for organ damage.
Area of Science:
- Immunology
- Biomarker Discovery
- Surgical Complications
Background:
- Postsurgical immunological complications, like systemic inflammation, lack effective diagnostic tools, impacting patient outcomes.
- Reliable immune monitoring is crucial for managing post-surgery inflammatory responses.
- Polymorphonuclear leukocytes (PMNs), particularly immature CD10-low PMNs, are implicated in early postsurgical inflammation.
Purpose of the Study:
- To investigate the role of CD10-low PMNs as an early diagnostic marker for postsurgical inflammation.
- To explore the correlation between CD10-low PMN counts and established inflammatory markers and organ damage indicators.
- To compare the characteristics of CD10-low PMNs with mature CD10-high PMNs.
Main Methods:
- Non-interventional exploratory study involving patients undergoing cardiac surgery with extracorporeal circulation.
- Quantification of CD10-low PMNs released post-surgery.
- Measurement of fluid phase markers of inflammation (CRP, IL-6) and organ damage (NGAL, CK-MB, troponin-T).
- Comparative analysis of CD10-low and CD10-high PMN expression (CD11b) and platelet-neutrophil complex (PNC) formation.
Main Results:
- The number of CD10-low PMNs correlated with postsurgical inflammation and organ damage markers.
- CD10-low PMN levels increased significantly 24 hours earlier than established markers like CRP and IL-6.
- CD10-low PMNs exhibited lower CD11b expression and reduced formation of platelet-neutrophil complexes compared to CD10-high PMNs.
Conclusions:
- CD10-low PMNs represent a promising early cellular biomarker for assessing postsurgical inflammatory response.
- These immature PMNs may offer superior early detection of inflammation compared to current markers.
- CD10-low PMNs could facilitate rapid immune monitoring for excessive inflammation and organ impairment risk.
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