Evidence map›Paper›PMID 23174342›Full record

ArticleBiological psychiatry2013

Inflammatory T helper 17 cells promote depression-like behavior in mice.

Eléonore Beurel, Laurie E Harrington, Richard S Jope

Open access · greenAbstract read
In one paragraph

Article in Biological psychiatry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 149 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
149citing papers in PubMed, 2 pooled it
1.8field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

149 citing papers in PubMed, 2 syntheses or guidelines pooled it, 242 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
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  10. Immunity in Rodent Models of Stress.Biological psychiatry · 2026
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. The emerging role of T cells in depression.Frontiers in psychiatry · 2026
    Review
  20. Article

89 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Eléonore BeurelDepartment of Psychiatry and Behavioral Sciences, and Biochemistry and Molecular Biology, Miller School of Medicine, University of Miami, Miami, Florida 33136, USA. ebeurel@med.miami.edu
Laurie E Harrington
Richard S Jope
University of Miami · USUniversity of Alabama at Birmingham · US

Funding

LITHIUM EFFECTS ON CHOLINERGIC ACTIVITYR01MH038752 · NIMH · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI JOPE, RICHARD S. · 1985 to 2015
$4.4M
Adaptive immune system function in depressionR01MH095380 · NIMH · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI JOPE, RICHARD S. · 2012 to 2016
$1.9M
Regulation of effector CD4 T cell subsets during inflammatory bowel diseaseR01DK084082 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HARRINGTON, LAURIE ELLEN · 2010 to 2014
$1.6M
Interactions Between Depression, Neuroinflammation and Glycogen Synthase Kinase-3R00MH090236 · NIMH · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BEUREL, ELEONORE · 2012 to 2014
$683k
Effects of lithium on cellular signalingR56MH038752 · NIMH · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI JOPE, RICHARD S. · 2011 to 2011
$366k
Interactions Between Depression, Neuroinflammation and Glycogen Synthase Kinase-3K99MH090236 · NIMH · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BEUREL, ELEONORE · 2010 to 2011
$179k
NIDDK NIH HHS R01 DK084082NIMH NIH HHS K99 MH090236NIMH NIH HHS MH038752NIMH NIH HHS MH090236NIMH NIH HHS MH095380NIMH NIH HHS R00 MH090236NIMH NIH HHS R01 MH038752NIMH NIH HHS R01 MH095380NIMH NIH HHS R56 MH038752
6 · The paper itself

Abstract

backgroundRecognition of substantial immune-neural interactions is revising dogmas about their insular actions and revealing that immune-neural interactions can substantially impact central nervous system functions. The inflammatory cytokine interleukin-6 promotes susceptibility to depression and drives production of inflammatory T helper 17 (Th17) T cells, raising the hypothesis that in mouse models, Th17 cells promote susceptibility to depression-like behaviors.

methodsBehavioral characteristics were measured in male mice administered Th17 cells, CD4(+) cells, or vehicle and in retinoid-related orphan receptor-γT (RORγT)(+/GFP) mice or male mice treated with RORγT inhibitor or anti-interleukin-17A antibodies.

resultsMouse brain Th17 cells were elevated by learned helplessness and chronic restraint stress, two common depression-like models. Th17 cell administration promoted learned helplessness in 89% of mice in a paradigm where no vehicle-treated mice developed learned helplessness, and impaired novelty suppressed feeding and social interaction behaviors. Mice deficient in the RORγT transcription factor necessary for Th17 cell production exhibited resistance to learned helplessness, identifying modulation of RORγT as a potential intervention. Treatment with the RORγT inhibitor SR1001, or anti-interleukin-17A antibodies to abrogate Th17 cell function, reduced Th17-dependent learned helplessness.

conclusionsThese findings indicate that Th17 cells are increased in the brain during depression-like states, promote depression-like behaviors in mice, and specifically inhibiting the production or function of Th17 cells reduces vulnerability to depression-like behavior, suggesting antidepressant effects may be attained by targeting Th17 cells.

Indexed as

AnimalsDepressionGene Knock-In TechniquesHelplessness, LearnedInflammationInterleukin-17MaleMiceNuclear Receptor Subfamily 1, Group F, Member 3Restraint, PhysicalSulfonamidesTh17 CellsThiazolesInterleukin-17Nuclear Receptor Subfamily 1, Group F, Member 3SR1001SulfonamidesThiazoles

Identifiers

PMID23174342
PMCPMC3582833
OpenAlexW2079562810

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.