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Published on: June 10, 2025
Immune status evaluation of patients with chronic heart failure
Pavlos M Myrianthefs1, Nikolaos Lazaris, Kyriaki Venetsanou
1Athens University School of Nursing ICU at KAT General Hospital, Kifissia, Athens, Greece. pmiriant@nurs.uoa.gr
Insights
Chronic heart failure patients exhibit both pro- and anti-inflammatory states, with altered cytokine production. This immune imbalance may worsen heart function and outcomes during infections.
Area of Science:
- Immunology
- Cardiology
- Biochemistry
Background:
- Chronic heart failure (CHF) is associated with immune activation and inflammation.
- Cytokines play a crucial role in inflammatory processes and disease progression.
Purpose of the Study:
- To compare the immune status of patients with CHF to healthy individuals.
- To investigate serum cytokine levels and ex vivo cytokine production in response to lipopolysaccharide (LPS).
Main Methods:
- Serum cytokine levels were measured in 14 CHF patients and 14 healthy volunteers.
- Whole blood samples were stimulated ex vivo with LPS (500 pg/ml) for 4 hours.
- Levels of TNF-RI, TNF-RII, TNF-alpha, IL-6, and IL-10 were quantified.
Main Results:
- CHF patients had higher serum levels of TNF-RI and TNF-RII compared to controls.
- After LPS stimulation, CHF patients showed higher TNF-alpha and IL-10, but lower IL-6 production.
- Endotoxin tolerance was not observed in CHF patients ex vivo.
Conclusions:
- Patients with CHF may exist in a dual pro- and anti-inflammatory state.
- Altered cytokine profiles, particularly increased TNF-alpha and IL-10 production, could contribute to disease severity and poorer outcomes in infections.
Abstract:
Chronic heart failure (CHF) may be considered a state of immune activation and persistent inflammation expressed by increased circulating levels of pro- and anti-inflammatory cytokines. The purpose of the study was to investigate the immune status in patients with CHF compared to normal individuals. We measured serum cytokine levels as well as cytokine production after ex vivo LPS stimulation of whole blood taken from 14 patients with CHF and 14 healthy volunteers. We used 500 pg/ml of LPS for an incubation period of 4h to stimulate 100 microL of whole blood. Patients with CHF had significantly higher levels of TNF-RI, and TNF-RII in serum compared to normal individuals. TNF-alpha, IL-6, and IL-10 did not differ significantly. After LPS stimulation, patients with CHF had significantly higher levels of TNF-alpha and IL-10, and significantly lower IL-6 levels compared to normal individuals. TNF-alpha receptors did not differ significantly. Patients with CHF may be found in a pro- as well as an anti-inflammatory state. They also do not develop endotoxin tolerance in an ex vivo laboratory model using whole blood stimulated with LPS. They may have increased TNF-alpha and IL-10 production after LPS stimulation of whole blood, which may contribute to a worsening of heart function, more severe disease presentation and a worse outcome during infections.
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