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Published on: December 2, 2015
PHA-stimulated cellular immune function and T-lymphocyte subsets in major depressive disorders
A Anesi1, D Franciotta, E Di Paolo
1Laboratory of Clinical Chemistry, IRCCS, C. Mondino Foundation, Univesity of Pavia, Italy.
Insights
Major depression is linked to reduced T-lymphocyte function, not cell count. This study found lower T-cell responses in depressed patients, suggesting functional immune changes characterize this disorder.
Area of Science:
- Immunology
- Neuroscience
- Psychiatry
Background:
- Major depressive disorder (MDD) is a prevalent mental health condition.
- The relationship between immune system function and MDD is complex and not fully understood.
- Previous research suggests potential immune dysregulation in depression.
Purpose of the Study:
- To investigate immunological parameters in patients with major depression.
- To compare T-lymphocyte subsets and function between depressed patients and healthy controls.
- To determine if numerical or functional changes in T-cells are associated with MDD.
Main Methods:
- Studied 20 hospitalized patients with MDD and 20 age/sex-matched healthy controls.
- Evaluated white blood cells using an automated cell counter.
- Assessed T-lymphocyte subpopulations via immunobead technique and T-cell function using a phytohemagglutinin-induced proliferation assay.
Main Results:
- T-lymphocyte responses to mitogen stimulation were significantly lower in depressed patients compared to controls.
- No significant differences were found in T-lymphocyte counts or other measured immunological parameters.
- Findings indicate a functional impairment in T-cell activity in individuals with MDD.
Conclusions:
- Functional, rather than numerical, alterations in T-lymphocytes may characterize major depressive disorder.
- Impaired T-cell responsiveness could play a role in the pathophysiology of depression.
- Further research is warranted to explore the clinical implications of these immune findings in MDD.
Abstract:
We measured some immunological parameters in 20 hospitalized patients with major depression and 20 age- and sex-matched healthy controls. Both enumeration of immune cells, including T-lymphocyte subpopulations, and assay of T-cell function were studied. White blood cells were evaluated with an automated cell counter, T-cell subsets with an immunobead technique, and T-cell function with a phytohemagglutinin-induced proliferation in vitro assay. We found that T-lymphocyte responses to the mitogen were significantly lower in depressed patients than in controls. All the other parameters were normal. These findings suggest that functional but not numerical changes in T-lymphocytes characterize major depressive disorders.
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