Evidence map›Paper›PMID 40962954›Full record

ArticleCellular & molecular immunology2025

The role of the IL-9‒NLRP3 axis in insulin resistance and adipose tissue inflammation during diet-induced obesity.

Marc P Hübner, Dennis de Coninck, Benjamin Lenz, Jayagopi Surendar, Marianne Koschel, Narcisse Victor Tchamatchoua Gandjui, Beng Amuam Andrew, Lucy Cho Nchang, Anita Obi Bate Ebob, Fanny Fri Fombad and 7 more

Abstract read
In one paragraph

Article in Cellular & molecular immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
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

17 authors.

Marc P HübnerInstitute for Medical Microbiology, Immunology and Parasitology, University Hospital Bonn, Bonn, Germany.ORCID 0000-0001-8885-418X
Dennis de ConinckInstitute of Pharmacology and Toxicology, University Hospital Bonn, Bonn, Germany.
Benjamin LenzInstitute for Medical Microbiology, Immunology and Parasitology, University Hospital Bonn, Bonn, Germany.
Jayagopi SurendarDepartment of Orthopedics and Trauma Surgery, University Hospital Bonn, Bonn, Germany.
Marianne KoschelInstitute for Medical Microbiology, Immunology and Parasitology, University Hospital Bonn, Bonn, Germany.
Narcisse Victor Tchamatchoua GandjuiParasite and Vector Biology Research Unit, Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Buea, Cameroon.ORCID 0000-0003-3314-4863
Beng Amuam AndrewParasite and Vector Biology Research Unit, Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Buea, Cameroon.
Lucy Cho NchangParasite and Vector Biology Research Unit, Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Buea, Cameroon.
Anita Obi Bate EbobParasite and Vector Biology Research Unit, Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Buea, Cameroon.
Fanny Fri FombadParasite and Vector Biology Research Unit, Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Buea, Cameroon.
Lisa Marie SpringerInstitute for Medical Microbiology, Immunology and Parasitology, University Hospital Bonn, Bonn, Germany.
Lars EppeUniversity of Oslo, Oslo, Norway.
Frank A SchildbergDepartment of Orthopedics and Trauma Surgery, University Hospital Bonn, Bonn, Germany.
Samuel WanjiParasite and Vector Biology Research Unit, Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Buea, Cameroon.
Achim HoeraufInstitute for Medical Microbiology, Immunology and Parasitology, University Hospital Bonn, Bonn, Germany.
Alexander PfeiferInstitute of Pharmacology and Toxicology, University Hospital Bonn, Bonn, Germany.
Indulekha KarunakaranInstitute for Medical Microbiology, Immunology and Parasitology, University Hospital Bonn, Bonn, Germany. Indulekha.Karunakaran@ukbonn.de.ORCID 0000-0002-4014-4880

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) EXC2151-390873048Deutsche Forschungsgemeinschaft (German Research Foundation) GZ: KA 5869/1-1Deutsche Forschungsgemeinschaft (German Research Foundation) HU 2144/3-1Deutsches Zentrum für Infektionsforschung (German Center for Infection Research) TTU 09.701Massachusetts Department of Fish and Game (DFG) EXC2151-390873048
6 · The paper itself

Abstract

Despite the proven beneficial role of type 2 cytokines in diabetes and obesity, IL-9, a predominant Th2 cytokine, has not been investigated in this context. The present study characterized the role of IL-9 signaling in obesity and metabolic dysfunction. We found decreased IL-9 levels in human type 2 diabetes patients and decreased IL-9 signaling in high-fat diet (HFD)-induced obese mice. On the other hand, recombinant IL-9 (rIL-9) treatment reversed insulin insensitivity and inflammation following HFD consumption. IL-9R knockout (KO) mice fed a HFD presented faster weight gain, impaired glucose and insulin tolerance, defective insulin signaling, increased adipocyte size, and decreased energy expenditure. In the adipose tissue of HFD-fed IL-9R KO mice, a significant increase in the number of CD11c+ macrophages and a decrease in the number of RELMα+ macrophages, eosinophils and ILC2s were observed, along with increased TNF, decreased adiponectin production and increased expression of NLRP3. In vitro treatment of human and mouse macrophages with rIL-9 decreased the release of NLRP3-induced IL-1β and IL-18. In vivo treatment of HFD-fed IL-9R KO mice with a pharmacological inhibitor of the NLRP3 inflammasome rescued body weight, insulin sensitivity and adipose tissue inflammation. Mechanistically, the STAT5 protein was found to be important for the IL-9-induced inhibition of the NLRP3 inflammasome in adipose tissue. In addition, we also demonstrated a potential role for IL-9 in the protective effects of helminth immunomodulation during obesity and insulin resistance in filaria-infected humans and in an animal model. Taken together, the results of this study highlight that IL-9 signaling improves insulin signaling by inhibiting NLRP3-induced inflammation.

Indexed as

Adipose TissueDiet, High-FatInflammationInsulin ResistanceInterleukin-9NLR Family, Pyrin Domain-Containing 3 ProteinObesityAnimalsDiabetes Mellitus, Type 2HumansMacrophagesMaleMiceMice, Inbred C57BLMice, KnockoutReceptors, Interleukin-9Interleukin-9NLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseReceptors, Interleukin-9HelminthsIL-9 signalingInflammasomeInflammationinsulin resistanceObesity

Identifiers

PMID40962954
PMCPMC12575696

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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.