CD4+ CD28(null) cells are an independent predictor of mortality in patients with heart failure
Lorenz Koller1, Bernhard Richter, Georg Goliasch
1Department of Internal Medicine II, Medical University of Vienna, Waehringer Guertel 18-20, 1090 Vienna, Austria.
Insights
Elevated levels of CD4(+)CD28(null) cells in chronic heart failure (CHF) patients predict increased mortality. These immune cells are linked to CHF severity, highlighting the immune system
Area of Science:
- Immunology
- Cardiology
- Pathophysiology
Background:
- Immune activation and proinflammatory cytokines are key in chronic heart failure (CHF) pathophysiology.
- CD4(+)CD28(null) cells, generated under inflammation, are linked to atherosclerosis and autoimmune diseases.
Purpose of the Study:
- To investigate the prognostic impact of CD4(+)CD28(null) cells on survival in patients with chronic heart failure.
Main Methods:
- Flow cytometry was used to analyze CD4 subsets in circulating lymphocytes from 107 CHF patients.
- Median follow-up was 23 months, during which all-cause and cardiovascular mortality were recorded.
Main Results:
- CD4(+)CD28(null) cells independently predicted all-cause mortality (HR 1.88) and cardiovascular mortality (HR 1.83).
- A significant association was found between CD4(+)CD28(null) cells and NT-proBNP levels (r=0.23).
Conclusions:
- Circulating CD4(+)CD28(null) cells are associated with CHF severity.
- These cells are a strong, independent predictor of mortality in CHF patients.
- The findings underscore the role of the immune system in CHF pathophysiology.
Aims:
Immune activation and subsequent release of proinflammatory cytokines plays a central role in the pathophysiology of chronic heart failure (CHF). Cytotoxic CD4(+)CD28(null) cells are generated under inflammatory conditions and implicated in a variety of pathological processes like atherosclerosis and autoimmune diseases. The study aim was to assess the impact of CD4(+)CD28(null) cells on survival in CHF patients.
Methods And Results:
Circulating lymphocytes from 107 CHF patients were analyzed for the distribution of CD4 subsets by flow cytometry. During a median follow-up of 23 months, 22 (20%) persons died. CD4(+)CD28(null) cells independently predicted all-cause mortality with an adjusted hazard ratio (HR) of 1.88 per 1-standard deviation increase (95% confidence interval (CI): 1.26-2.79, P = 0.002) and with a HR of 1.83 for cardiovascular mortality (95% CI: 1.18-2.86, P = 0.008), respectively. Further, we found a significant association with NT-proBNP (r = 0.23).
Conclusion:
Circulating CD4(+)CD28(null) cells are associated with CHF severity and are a strong and independent predictor of mortality in CHF fostering the implication of the immune system in CHF pathophysiology.
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