Related Experiment Video
Updated: Aug 16, 2026

Flow Cytometry-based Assay for the Monitoring of NK Cell Functions
Published on: October 30, 2016
Functional abnormalities of circulating natural killer cell subpopulations in patients with dilated cardiomyopathy
T Kanda1, T Yokoyama, T Suzuki
1Second Department of Internal Medicine, Gunma University School of Medicine.
Insights
Natural killer (NK) cells in the heart muscle were increased in dilated cardiomyopathy (DCM) patients. Fewer NK cells were found in DCM patients who died, suggesting functional NK cell abnormalities in DCM pathogenesis.
Area of Science:
- Immunology
- Cardiology
- Cell Biology
Background:
- Idiopathic dilated cardiomyopathy (DCM) is a complex heart condition with unclear pathogenesis.
- Natural killer (NK) cells are crucial immune cells with roles in viral infections and cancer, but their involvement in cardiac diseases is less understood.
Purpose of the Study:
- To investigate the role of NK cells in the myocardium and peripheral blood of patients with DCM.
- To determine if NK cell abnormalities correlate with disease severity or prognosis in DCM.
Main Methods:
- Immunohistochemical staining of myocardial biopsies to quantify CD57-positive NK cells.
- Analysis of peripheral blood NK cell activity and subset populations.
- Comparison of NK cell findings between DCM patients, other cardiomyopathies, and healthy controls.
Main Results:
- Significantly higher numbers of CD57-positive NK cells were found in the myocardium of DCM patients compared to controls.
- DCM patients who died within five years had significantly fewer myocardial CD57-positive NK cells than survivors.
- No significant differences in peripheral NK cell activity or subset numbers were observed between DCM patients and controls, but correlations found in controls were absent in DCM patients.
Conclusions:
- Functional abnormalities in NK cell subpopulations may exist in DCM patients.
- These NK cell abnormalities could be implicated in the pathogenesis of DCM.
- Myocardial NK cell presence, specifically CD57+ cells, may serve as a prognostic indicator in DCM.
Abstract:
We investigated abnormalities in natural killer (NK) cells in the myocardium and circulating blood of 38 patients with idiopathic dilated cardiomyopathy (DCM), 18 patients with hypertrophic cardiomyopathy, 8 patients with primary amyloidosis, and 12 age-matched normal control subjects. Immunohistochemical staining of myocardial biopsies revealed a significantly greater number of CD57-positive NK cells in patients with DCM than that in controls (3.7 +/- 2.7 v.s. 1.9 +/- 1.6, p < 0.05). The New York Heart Association functional class, left ventricular ejection fraction, myocardial fiber diameter, and interstitial fibrosis volume fraction did not differ significantly between the DCM patients who died within five years of diagnosis and the 31 surviving DCM patients. However, there were significantly fewer CD57-positive NK cells in patients who died than in surviving patients (p < 0.05). There were no significant differences in the peripheral NK cell activity or the number of NK subset cells between the 16 patients with DCM (n = 16) and the 12 age-matched normal controls. In normal controls, the number of some NK cell subpopulations (CD16+, CD57+, CD16+ CD57+, and CD8+ CD57+ cells) were positively correlated with NK cell activity. In patients with DCM, there was no correlation between the number of NK cell subpopulations and NK cell activity. Our findings indicate that functional abnormalities exist in NK cell subpopulations in patients with DCM, and that these abnormalities may be related to the pathogenesis of DCM.
Related Concept Videos
Myocarditis I: Introduction
Cardiomyopathy II: Dilated Cardiomyopathy
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy IV: Restrictive Cardiomyopathy

