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Increased CD56+ natural killer cells and related cytokines in major depression
A Seidel1, V Arolt, M Hunstiger
1Institute of Immunology and Transfusion Medicine, University of Lübeck School of Medicine, Germany.
Insights
Major depression patients exhibit elevated CD56+ natural killer (NK) cell counts and enhanced lymphokine production. This correlation was significant during acute illness but diminished with clinical improvement.
Area of Science:
- Immunology
- Neuroscience
- Psychiatry
Background:
- Major depression is a complex disorder with potential immune system dysregulation.
- Natural killer (NK) cells and their associated lymphokines play roles in immune function and mood disorders.
Purpose of the Study:
- To investigate CD56+ NK cell counts and lymphokine production (interleukin-2, interferon-gamma) in major depression patients.
- To explore the relationship between NK cell activity and clinical status in depression.
Main Methods:
- Flow cytometry was used to quantify CD56+ NK cell counts in 27 inpatients over 6 weeks.
- Whole blood assays measured interleukin-2 and interferon-gamma responses to phytohemagglutinin (PHA) stimulation.
Main Results:
- Patients with major depression showed significantly higher CD56+ NK cell counts compared to controls.
- A greater lymphokine response to PHA was observed in patients during their acute clinical stage.
- A significant correlation between lymphokine secretion and CD56+ NK cell counts was found in the acute phase of depression.
Conclusions:
- Elevated CD56+ NK cell counts and enhanced lymphokine production are associated with the acute phase of major depression.
- The correlation between NK cell activity and lymphokine secretion suggests a role for these immune components in depression pathophysiology.
- Immune markers may normalize with clinical improvement, indicating a dynamic relationship between depression and immune function.
Abstract:
Twenty-seven inpatients with major depression were examined four times within 6 weeks to assess CD56+ natural killer (NK) cell counts by flow cytometry and to assess the related lymphokines interleukin-2 and interferon-gamma in a whole blood assay after mitogen stimulation with phytohemagglutinin (PHA). The patient showed significantly higher counts of the fraction of 56+ NK cells and a greater lymphokine response to PHA than the controls. A significant correlation between lymphokine secretion and CD56+ cell counts was detected in the patients' acute clinical stage, but not in healthy controls or in patients after clinical improvement.
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