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Updated: May 18, 2026

On-Chip Endothelial Inflammatory Phenotyping
Published on: July 21, 2012
Endothelial Activation Phenotypes and Interleukin-6 Response After Therapeutic Plasma Exchange in Severe
Nicoleta Sgavardea1, Ovidiu Bedreag2, Greeshmasree Kambam3
1Doctoral School, "Victor Babes" University of Medicine and Pharmacy, Eftimie Murgu Square 2, 300041 Timisoara, Romania.
Background And Objectives:
Severe COVID-19 frequently fulfills Sepsis-3 criteria and is characterized by thrombo-inflammation and endothelial injury. We evaluated whether a bedside endothelial activation index (EAI = D-dimer/fibrinogen) identifies biologically distinct phenotypes and relates to interleukin-6 (IL-6) response after therapeutic plasma exchange (TPE), and whether baseline IL-6 predicts a ≥50% IL-6 reduction.
Methods:
Retrospective single-center ICU cohort of adults with SARS-CoV-2 infection, sepsis-related organ dysfunction, and ≥1 TPE session (n = 51). Patients were stratified by median EAI (low vs. high). Outcomes included peri-procedural biomarker/physiology changes (post-baseline), IL-6 responder status (≥50% reduction), correlations with IL-6 reduction (%), and multivariable predictors of response.
Results:
Compared with low EAI (n = 25), high EAI (n = 26) had higher baseline D-dimer (6.2 vs. 2.2 µg/mL) and lower fibrinogen (2.9 vs. 7.1 g/L) (both p < 0.001). Low EAI showed larger CRP decreases (ΔCRP -84.0 vs. -2.3 mg/L; p = 0.001) and larger fibrinogen falls (Δ -3.1 vs. -0.4 g/L; p < 0.001), while high EAI had larger D-dimer decreases (Δ -2.5 vs. -0.6 µg/mL; p = 0.004) and a modest SOFA improvement (Δ -0.3 vs. +0.1; p = 0.026). IL-6 responders (n = 20) had higher baseline IL-6 than non-responders (365.2 vs. 47.1 pg/mL; p < 0.001). Baseline IL-6 independently predicted response (per doubling: OR 1.94, 95% CI 1.27-2.95; p = 0.002), while age reduced odds (OR 0.91/year, 95% CI 0.84-0.99; p = 0.032). IL-6 reduction correlated with ΔCRP (ρ = -0.41; p = 0.003) and ΔPaO2/FiO2 (ρ = 0.37; p = 0.01).
Conclusions:
EAI stratifies distinct thrombo-inflammatory patterns around TPE, while baseline IL-6 is the dominant predictor of achieving large IL-6 reductions. To emphasize the novelty and clarify the study objective, this exploratory analysis used a phenotype-stratified framework to test whether a simple bedside endothelial activation index could enrich biological response assessment to adjunctive TPE. The prespecified primary outcome was achievement of a ≥50% IL-6 reduction after completion of the TPE course; secondary outcomes included peri-procedural biomarker, oxygenation, SOFA, and ICU endpoints.
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