[Characteristics of immune response and inflammatory reaction in atherothrombotic stroke and myocardial infarction]
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Updated: Mar 24, 2026

Isolation and Flow Cytometric Analysis of Immune Cells from the Ischemic Mouse Brain
Published on: February 12, 2016
E V Konstantinova1, A G Kochetov1, N A Shostak1
1Pirogov Russian National Research Medical University, Moscow.
Insights
Markers of immune response, inflammation, and apoptosis are elevated in myocardial infarction (MI) and atherothrombotic stroke (AS), indicating shared mechanisms in ischemic tissue damage. Specific correlations between these markers were identified in the acute phase.
Area of Science:
- Biochemistry
- Immunology
- Pathophysiology
Context:
- Myocardial infarction (MI) and atherothrombotic stroke (AS) are leading causes of mortality and morbidity.
- Understanding the underlying mechanisms of ischemic tissue damage is crucial for developing effective treatments.
Purpose:
- To investigate the correlations between markers of immune response, inflammation, and apoptosis in patients with MI and AS.
- To characterize ischemic tissue damage by assessing these marker relationships.
Summary:
- This study measured levels of matrix metalloproteinase-9 (MMP-9), immune complexes, soluble Fas-ligand, tumor necrosis factor alpha, and interleukin-10 in patients with MI and AS.
- Flow cytometry was used to assess apoptosis, Toll-like receptors-4, and heat shock proteins.
- Elevated levels of immune response, inflammation, and apoptosis markers were observed in the early stages of MI and AS.
Impact:
- Identifies shared pathophysiological mechanisms in ischemic tissue damage in both MI and AS.
- Highlights the specificity of marker relationships in the acute phase of these conditions.
- Provides a novel approach to assessing the role of these parameters in acute myocardial ischemia and brain injury.
Aim:
To study characteristics of ischemic tissue damage basing on the assessment of the correlations between markers of immune response, inflammation and apoptosis in patients with myocardial infarction (MI) and atherothrombotic stroke (AS).
Material And Methods:
Concentrations of matrix metalloproteinase-9 (MMP-9), immune complexes with cryogenic properties, soluble Fas-ligand, tumor necrosis factor alpha, interleukin-10 measured with ELISA as well as the activity of spontaneous apoptosis of mononuclear cells and surface expression of Toll-like receptors-4 and intracellular heat shock proteins measured with flow cytofluorometry were determined in the blood of 93 patients with the first AS and 94 patients with MI without concomitant inflammation in the 1st and 7th day of the disease.
Results And Conclusion:
Increased levels of the markers of immune response, inflammation, apoptosis and destruction of the extracellular matrix were identified at the beginning of MI and AS. The results provide the evidence that similar mechanisms may be involved in ischemic tissue damage. Multivariate analysis conducterd by of principal component analysis correlation matrix revealed the specificity of the relationships between all of these markers. This is the completely new approach to assessin the role and importance of defined parameters in the acute period of the myocardial ischemia and brain.
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