Immune-endocrine host response to endotoxin in major depression
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…
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
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]
No citation lists for this paper
No citation lists for this paper yet — checked again daily.
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
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review