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Intracellular Staining and Flow Cytometry to Identify Lymphocyte Subsets within Murine Aorta, Kidney and Lymph Nodes in a Model of Hypertension
Published on: January 28, 2017
Lymphocyte subset characterization in patients with early clinical presentation of coronary heart disease
Natale Daniele Brunetti1, Carmine D'Antuono, Michele Rana
1Cardiology Department, University of Foggia, Viale Pinto 1, 71100, Foggia, Italy. nd.brunetti@unifg.it
Insights
Early coronary heart disease (CHD) patients exhibit altered T-lymphocyte populations, specifically a lower CD3+ count and an increased CD4+/CD8+ ratio. These immune changes correlate with disease severity and impaired heart function.
Area of Science:
- Immunology
- Cardiology
- Biochemistry
Background:
- Coronary heart disease (CHD) is a leading cause of mortality worldwide.
- Immune system dysregulation may play a role in the pathogenesis of CHD.
- Lymphocyte subset alterations have been observed in various cardiovascular conditions.
Purpose of the Study:
- To investigate lymphocyte populations (CD3+, CD19+, CD4+, CD8+) in non-diabetic patients with early clinical presentation of CHD.
- To explore the relationship between lymphocyte subsets, left ventricular ejection fraction, and coronary atherosclerosis severity.
Main Methods:
- Flow cytometry was used to determine lymphocyte populations in 25 CHD patients and 25 matched controls.
- Exclusion criteria included diabetes, heart failure symptoms, and recent revascularization.
- Coronary angiography was performed on all CHD patients.
Main Results:
- CHD patients showed significantly lower CD3+ (T-lymphocytes) and CD8+ (suppressor/cytotoxic lymphocytes) levels.
- CHD patients exhibited higher CD4+ (helper/inducer lymphocytes) levels and an elevated CD4+/CD8+ ratio.
- Lower CD8+ and higher CD4+/CD8+ ratios were observed in patients with impaired left ventricular ejection fraction; CD8+ levels inversely correlated with coronary atherosclerosis severity.
Conclusions:
- Early clinical presentation of CHD is associated with altered lymphocyte populations, including a reduced CD3+ count and an increased CD4+/CD8+ ratio.
- These immune alterations may be linked to disease progression and cardiac dysfunction in CHD patients.
Abstract:
This study aimed to investigate lymphocyte populations in non-diabetic patients with early clinical presentation of coronary heart disease (CHD). Twenty-five consecutive middle-aged (<55 years) out-patients with CHD (acute myocardial infarction in the previous 3 months) and stable clinical conditions (>1 month) underwent venous blood sampling in order to determinate CD3+ (T-lymphocytes), CD19+ (B-lymphocytes), CD4+ (helper/inducer lymphocytes) and CD8+ (suppressor/cytotoxic lymphocytes) populations. Patients with diabetes, heart failure symptoms, recent revascularization (<30 days) were excluded. Twenty-five patients matched for age, gender and risk factors were enrolled as controls. All patients with CHD previously underwent coronary angiography. CHD patients showed lower CD3+ levels (70.96 ± 4.72 vs. 74.12 ± 4.93 %, p < 0.05) and CD8+ (37.80 ± 7.15 vs. 46.36 ± 5.22 %, p < 0.001) but higher CD4+ (37.32 ± 7.99 vs. 31.64 ± 4.72 %, p < 0.01) and CD4+/CD8+ ratio (1.06 ± 0.43 vs. 0.69 ± 0.13, p < 0.001). Difference in CD19+ levels was not statistically significant. Subjects with an impaired (≤55 %) left ventricular ejection fraction were characterized by lower levels of CD8+ (33.23 ± 7.04 vs. 43.76 ± 7.40 %, p < 0.05) and higher levels of CD4+ (38.31 ± 8.23 vs. 32.73 ± 6.08 %, p < 0.05) and CD4+/CD8+ ratio (1.06 ± 0.38 vs. 0.79 ± 0.34, p < 0.05). CD8+ levels inversely related to severity of coronary atherosclerosis (r = -0.37, p < 0.01). In conclusion, subjects with early clinical presentation of CHD are characterized by an altered CD4+/CD8+ ratio and lower CD3+ levels.
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