Depression and suicidality: A link to premature T helper cell aging and increased Th17 cells
Abstract
Background Previous research has demonstrated a strong link between immune system abnormalities and Major Depressive Disorder (MDD). High suicide risk is a major complication of MDD and has recently been linked to strong (neuro-)immune alterations, but little is known on the link between circulating immune cell composition and suicidal risk status.Methods Here, we assessed percentages of circulating peripheral blood mononuclear cells with focus on T helper cell subsets (memory T helper cells, Th1, Th2, Th17 and T regulatory cells) in a large and well-matched cohort of 153 patients diagnosed with MDD and 153 age and sex matched controls. We explored the association of these cell populations with suicide risk while accounting for age, sex, BMI, depression severity and childhood trauma.Results Patients with MDD had reduced percentages of NK cells, and higher percentages of B and T cells in line with current literature. Further exploration of T-cells revealed a robustly elevated number of memory T helper cells, regardless of age group. Patients at high risk for suicide had the highest memory T helper cells and additionally showed a robust increase of Th17 cells compared to other suicide risk groups.Conclusions The higher abundance of memory T helper cells points towards premature aging of the immune system in MDD patients, even during young adulthood. Patients at high risk for suicide show the clearest immune abnormalities and may represent a clinically relevant subtype of depression.
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Peripheral T helper (Th) cells can be a potential biomarker for the early prediction of depression.
“A recent clinical study strongly suggested that peripheral T helper (Th) cells can be a potential biomarker for the early prediction of depression [14].”
From Chronic stress-induced depression requires the recruitment of peripheral Th17 cells into the brain (2022) · cites this paper as [14]
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References 60 · Cited by 114
- Authors
- Schiweck, C., Valles-Colomer, M., Arolt, V., Müller, N., Raes, J., Wijkhuijs, A., Claes, S., Drexhage, H., & Vrieze, E.
- Affiliations
- KU Leuven (BE)
- University of Münster (DE)
- Ludwig-Maximilians-Universität München (DE)
- Rega Institute for Medical Research (BE)
- Erasmus MC (NL)
- Corresponding author
- Schiweck, Carmen
- ORCID
- Venue
- Brain, Behavior, and Immunity
- Publisher
- Elsevier BV
- Published
- 2020-07
- Volume
- 87
- Pages
- 603-609
- ISSN
- 0889-1591 (ISSN-L)
- OpenAlex
- W3005609732
- Cited by
- 114
- References
- 60
- Citations by year
- 2026: 11 · 2025: 21 · 2024: 30 · 2023: 18 · 2022: 17 · 2021: 11 · 2020: 6
- FWCI
- 3.94
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Brain Behavior and Immunity (publishedVersion)
- PubMed (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
- Lirias (submittedVersion)
- Funders
- Horizon 2020 Framework Programme
- Seventh Framework Programme
- Topics
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Social Sciences › Psychology › Clinical Psychology › Suicide and Self-Harm Studies
- Keywords
- major depressive disorder, suicide risk, Th17 cells, immunosenescence, T helper cell subsets, natural killer cells, regulatory T cells, Th1/Th2 cells, depression subtypes
- MeSH terms
- Adult, Aging, Child, Depression, Major Depressive Disorder, Humans, Leukocytes, Mononuclear, Suicide, Th1 Cells, Th2 Cells, Aging, Premature, T-Lymphocytes, Regulatory, Young Adult, Th17 Cells
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