Cited by 27Stress Responses and CortisolTryptophan and brain disordersTreatment of Major Depression

Immune-endocrine host response to endotoxin in major depression

Vedder, Helmut, Schreiber, Wolfgang, Schuld, Andreas, Kainz, Martin, Lauer, Christoph Johannes, Krieg, Jürgen-Christian, Holsboer, Florian, Pollmächer, Thomas·2007·Journal of Psychiatric Research

Abstract

Objective An impaired hypothalamic-pituitary-adrenocortical (HPA) function is a well-established finding in major depression (MD), but it is still unclear how this dysfunction affects immune responses in this disorder. Method To further examine the relationship between immune and endocrine responses in MD, 0.4ng/kg body weight endotoxin [LPS] or 100mug hCRH were sequentially applied to 12 patients with MD and to 12 age- and gender-matched healthy controls after pre-treatment with 1.5mg dexamethasone (DEX). Immune (TNF-alpha, IL-6, rectal temperature) and endocrine (ACTH, cortisol) parameters were examined as area under the curve (AUC) levels. Results After pre-treatment with DEX, LPS evoked an immune response in all participants of the study with most immune parameters significantly related to the endotoxin challenge. However, only a marked immune response resulted in an additional endocrine reaction. Subsequently, the quantitative extent of the endocrine reaction was related to the extent of the immune response after DEX/LPS challenge. Pre-LPS AUC levels of cortisol, ACTH and post-LPS levels of IL-6 as well as the post-CRH AUC levels of cortisol and ACTH were related to the depressive symptomatology as measured by the Beck depression inventory (BDI). In depressive patients who showed increased cortisol plasma levels before LPS, the later increase in IL-6 was reduced. Conclusions The challenge with DEX/LPS did not reveal major impairments of evoked immune functions in MD. Onl…

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Crossref · 10.1016/j.jpsychires.2006.07.014

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  • In a study examining the neuroendocrine and immune responses to lipopolysaccharide (LPS) following DEX administration, subjects with evidence of glucocorticoid resistance exhibited increased cytokine (IL-6 and TNF-α) responses regardless of whether they were depressed or not.

    “subjects with evidence of glucocorticoid resistance (as manifested by increased ACTH and cortisol responses) exhibited increased cytokine (IL-6 and TNF-α) responses regardless of whether they were depressed or not”

    From Cytokines and Glucocorticoid Receptor Signaling (2009) · cites this paper as [88]

  • This indicates that the relationship between HPA axis sensitivity to glucocorticoids and responsiveness of the innate immune system may be unrelated to diagnosis.

    “indicating that the relationship between HPA axis sensitivity to glucocorticoids and responsiveness of the innate immune system may be unrelated to diagnosis.88”

    From Cytokines and Glucocorticoid Receptor Signaling (2009) · cites this paper as [88]

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References 58 · Cited by 27

Authors
Vedder, H., Schreiber, W., Schuld, A., Kainz, M., Lauer, C. J., Krieg, J.-C., Holsboer, F., & Pollmächer, T.
Affiliations
Max Planck Institute of Psychiatry (DE)
Corresponding author
Vedder, Helmut
Venue
Journal of Psychiatric Research
Publisher
Elsevier BV
Published
2007-04
Volume
41
Issue
3-4
Pages
280-289
ISSN
0022-3956 (ISSN-L)
OpenAlex
W2105947568
Cited by
27
References
58
Citations by year
2026: 1 · 2025: 1 · 2024: 1 · 2022: 1 · 2020: 1 · 2019: 1 · 2018: 1 · 2017: 1 · 2016: 1 · 2015: 1 · 2014: 1 · 2012: 4
FWCI
1.09
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Psychiatric Research (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
  • Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
  • Health Sciences › Medicine › Pharmacology › Treatment of Major Depression
Keywords
major depressive disorder, endotoxin challenge, lipopolysaccharide, hypothalamic-pituitary-adrenal axis, immune response, interleukin-6, TNF-α, cortisol, ACTH, dexamethasone, corticotropin-releasing factor, endocrine-immune interaction, depressive symptoms
MeSH terms
Adrenocorticotropic Hormone, Adult, Analysis of Variance, Body Temperature, Corticotropin-Releasing Hormone, Major Depressive Disorder, Dexamethasone, Endocrine System, Endotoxins, Female, Humans, Hydrocortisone, Immunity, Lipopolysaccharides, Male, Middle Aged, Time Factors, Tumor Necrosis Factor-alpha, Interleukin-6, Case-Control Studies, Area Under Curve

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