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Published on: August 1, 2014
[Detection of soluble endothelial protein C receptor (sEPCR) in patients with CHD, DM and SLE]
Insights
Plasma soluble endothelial protein C receptor (sEPCR) levels are elevated in patients with diabetes mellitus (DM) and systemic lupus erythematosus (SLE). This finding suggests a link between sEPCR, inflammation, and endothelial cell damage in these conditions.
Area of Science:
- Biochemistry
- Immunology
- Cardiovascular Medicine
Background:
- Endothelial protein C receptor (EPCR) plays a role in the protein C anticoagulant pathway.
- Soluble EPCR (sEPCR) is a circulating form of EPCR with potential implications in various diseases.
Purpose of the Study:
- To investigate the clinical significance of plasma sEPCR levels.
- To compare sEPCR levels in patients with coronary heart disease (CHD), diabetes mellitus (DM), and systemic lupus erythematosus (SLE) against normal controls.
Main Methods:
- Enzyme-linked immunosorbent assay (ELISA) was employed to quantify sEPCR.
- Plasma samples were analyzed from patients with CHD (n=34), DM-II (n=42), SLE (n=63), and normal controls (NC, n=20).
Main Results:
- Plasma sEPCR levels were significantly higher in patients with DM compared to NC (P < 0.05).
- SLE patients, both with and without thrombosis, exhibited elevated sEPCR levels compared to NC (P < 0.005 and P < 0.001, respectively).
- No significant difference in sEPCR levels was observed between CHD and NC groups, or between SLE subgroups.
Conclusions:
- Elevated plasma sEPCR levels are associated with DM and SLE.
- Increased sEPCR may indicate inflammatory processes and endothelial cell damage in these conditions.
- sEPCR warrants further investigation as a potential biomarker in DM and SLE.
Objective:
To evaluate the clinical significance of plasma soluble endothelial protein C receptor (sEPCR) level in patients with coronary heart disease (CHD), diabetes mellitus (DM) and systemic lupus erythematosus (SLE).
Methods:
ELISA of antibody-sandwiched principle was used to detect sEPCR in 34 patients with CHD, 42 with DM-II, 63 with SLE and 20 normal controls (NC).
Results:
The plasma level of sEPCR in patients with DM was higher than that in NC group (P < 0.05). The sEPCR level in SLE patients with thrombosis and non-thrombosis are higher than that in NC group (P < 0.005 and P < 0.001, respectively). There is no significant difference between the two groups of SLE (P > 0.05), and between the CHD and NC groups.
Conclusion:
sEPCR level increased in DM and SLE, it seems related to the process of inflammatory reaction and damage of endothelial cell.
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