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Quantification of Monocyte Transmigration and Foam Cell Formation from Individuals with Chronic Inflammatory Conditions
Published on: October 17, 2017
Activation of CD14 on circulating monocytes in patients with acute coronary syndrome
Insights
Inflammation plays a key role in acute coronary syndrome (ACS). Monocyte CD14 expression and T-lymphocyte activation markers were elevated in ACS patients, decreasing with treatment, indicating their value in assessing disease status.
Area of Science:
- Cardiovascular Medicine
- Immunology
- Biochemistry
Background:
- Inflammation is increasingly recognized as a critical factor in the acute phase of coronary artery diseases.
- Understanding inflammatory markers can provide insights into disease mechanisms and progression.
Purpose of the Study:
- To investigate the activation status of inflammatory cells in patients with acute coronary syndrome (ACS).
- To evaluate specific markers, CD14 expression on monocytes and HLA-DR on T-lymphocytes, as indicators of inflammation in ACS.
Main Methods:
- Flow cytometry was used to analyze inflammatory cell activation in 38 ACS patients, 14 stable angina patients, and 19 controls.
- Monocyte activation was assessed by CD14 expression, and T-lymphocyte activation by HLA-DR positivity.
- Tumor necrosis factor-alpha secretion was measured after lipopolysaccharide stimulation.
Main Results:
- ACS patients exhibited significantly higher CD14 expression on monocytes and HLA-DR positive T-lymphocytes compared to controls and stable angina patients.
- A 2.4-fold higher secretion of tumor necrosis factor-alpha was observed in ACS patients.
- Following medical treatment, significant reductions in both CD14 expression and HLA-DR positive T-lymphocytes were noted in ACS patients.
Conclusions:
- Elevated monocytic CD14 expression in ACS patients indicates activated monocytes and hyper-responsiveness.
- CD14 expression levels decrease with treatment, confirming its utility in reflecting monocyte activation during acute coronary artery disease.
- These markers are valuable for assessing inflammatory status in ACS.
Background:
Increasing evidence supports the involvement of inflammation in acute phase of coronary artery diseases.
Methods:
We analyzed the status of activation of inflammatory cells in 38 patients with acute coronary syndrome, 14 stable angina patients, and 19 control subjects by flow-cytometry. Expression levels of CD14 and the percentage of HLA-DR(+) T-lymphocytes were used as markers of monocyte and T-lymphocytes activation, respectively.
Results:
The expression of CD14 on monocytes in acute coronary syndrome patients (mean fluorescence intensity+/-S.D.=158.1+/-77.1) was increased significantly in comparison to control subjects (57.1+/-8.0) and the stable angina group (63.6+/-22.0) (P<0.0001 for both). A significantly higher percentage of HLA-DR positive T-lymphocytes (20.4+/-9.0 vs. 12.7+/-3.7%, P<0.01) was observed in acute coronary syndrome patients in comparison to control subjects. Incubation of whole blood cells with bacterial lipopolysaccharide resulted in a 2.4-fold higher secretion of tumor necrosis factor-alpha in acute coronary syndrome patients than in control subjects (P<0.05). When these markers of activation were measured in acute coronary syndrome patients 6 weeks after medical treatment, a significant reduction both in monocytic CD14 expression and percentage of HLA-DR positive T-lymphocytes (P<0.05 for both) was observed.
Discussion:
We observed markedly increased levels of monocytic CD14 expression in ACS patients, which appear to indicate the activated status of monocytes and hyper-responsiveness to external stimuli. The CD14 expression levels decreased as the patients were treated, indicating that the expression of CD14 accurately represents the activation status of monocytes during the acute phase of coronary artery diseases.
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