Evidence map›Paper›PMID 34394118›Full record

ArticleFrontiers in immunology2021

Pathogenetic Interplay Between IL-6 and Tryptophan Metabolism in an Experimental Model of Obesity.

Giada Mondanelli, Elisa Albini, Elena Orecchini, Maria Teresa Pallotta, Maria Laura Belladonna, Giovanni Ricci, Ursula Grohmann, Ciriana Orabona

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.0field-weighted citation impact, top 32% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. Gut microbes · 2026
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  5. Exploratory Cohort Study of Depressive Symptoms in South Africans with HIV-1 Subtype C: Associations with Kynurenine Pathway Metabolites and Inflammatory Markers.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2026
    Article
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  11. Bridging the divide: unveiling mutual immunological pathways of cancer and pregnancy.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Giada MondanelliDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.
Elisa AlbiniDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.
Elena OrecchiniDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.
Maria Teresa PallottaDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.
Maria Laura BelladonnaDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.
Giovanni RicciService Center for Pre-clinical Research, University of Perugia, Perugia, Italy.
Ursula GrohmannDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.
Ciriana OrabonaDepartment of Medicine and Surgery, University of Perugia, Perugia, Italy.
University of Perugia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Obesity is a metabolic disease characterized by a state of chronic, low-grade inflammation and dominated by pro-inflammatory cytokines such as IL-6. Indoleamine 2,3-dioxygenase 1 (IDO1) is an enzyme that catalyzes the first step in the kynurenine pathway by transforming l-tryptophan (Trp) into l-kynurenine (Kyn), a metabolite endowed with anti-inflammatory and immunoregulatory effects. In dendritic cells, IL-6 induces IDO1 proteasomal degradation and shuts down IDO1-mediated immunosuppressive effects. In tumor cells, IL-6 upregulates IDO1 expression and favors tumor immune escape mechanisms. To investigate the role of IDO1 and its possible relationship with IL-6 in obesity, we induced the disease by feeding mice with a high fat diet (HFD). Mice on a standard diet were used as control. Experimental obesity was associated with high IDO1 expression and Kyn levels in the stromal vascular fraction of visceral white adipose tissue (SVF WAT). IDO1-deficient mice on HFD gained less weight and were less insulin resistant as compared to wild type counterparts. Administration of tocilizumab (TCZ), an IL-6 receptor (IL-6R) antagonist, to mice on HFD significantly reduced weight gain, controlled adipose tissue hypertrophy, increased insulin sensitivity, and induced a better glucose tolerance. TCZ also induced a dramatic inhibition of IDO1 expression and Kyn production in the SVF WAT. Thus our data indicated that the IL-6/IDO1 axis may play a pathogenetic role in a chronic, low-grade inflammation condition, and, perhaps most importantly, IL-6R blockade may be considered a valid option for obesity treatment.

Indexed as

Disease SusceptibilityEnergy MetabolismAdipose TissueAnimalsBiomarkersCytokinesDiet, High-FatDisease Models, AnimalHepatocytesIndoleamine-Pyrrole 2,3,-DioxygenaseInsulinInterleukin-6KynurenineMaleMiceObesityBiomarkersCytokinesIndoleamine-Pyrrole 2,3,-DioxygenaseInsulinInterleukin-6KynurenineReceptors, Interleukin-6Tryptophanexperimental obesityhigh fat diet (HFD)IL-6 receptor (IL-6R)indoleamine 2, 3 dioxygenase 1 (IDO1)tocilizumab (TCZ)tryptophan metabolismwhite adipose tissue (WAT)

Identifiers

PMID34394118
PMCPMC8361489
OpenAlexW3192401945

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.