Evidence map›Paper›PMID 26425820›Full record

ArticleImmunology2016

Interferon-γ constrains cytokine production of group 2 innate lymphoid cells.

Fujimi Kudo, Masashi Ikutani, Yoichi Seki, Takeshi Otsubo, Yuki I Kawamura, Taeko Dohi, Kenshiro Oshima, Masahira Hattori, Susumu Nakae, Kiyoshi Takatsu and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Development of Adaptive Immunity and Its Role in Lung Remodeling.Advances in experimental medicine and biology · 2023
    Article
  8. Viral PB1-F2 and host IFN-γ guide ILC2 and T cell activity during influenza virus infection.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  9. Innate Lymphoid Cells in Renal Inflammation.Frontiers in immunology · 2020
    Review
  10. Review
  11. Article
  12. Prostaglandin EFrontiers in immunology · 2018
    Article
  13. Article
  14. Review
  15. IL-33/ST2 Axis in Organ Fibrosis.Frontiers in immunology · 2018
    Review
  16. Pathways to limit group 2 innate lymphoid cell activation.The Journal of allergy and clinical immunology · 2017
    Article
  17. Article
  18. 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

11 authors at 4 institutions in 1 country.

Fujimi KudoDepartment of Immune Regulation, Research Centre for Hepatitis and Immunology, Research Institute, National Centre for Global Health and Medicine, Chiba, Japan.
Masashi IkutaniDepartment of Immunobiology and Pharmacological Genetics, Graduate School of Medicine and Pharmaceutical Science for Research, University of Toyama, Toyama, Japan.
Yoichi SekiDepartment of Immune Regulation, Research Centre for Hepatitis and Immunology, Research Institute, National Centre for Global Health and Medicine, Chiba, Japan.
Takeshi OtsuboDepartment of Gastroenterology, Research Centre for Hepatitis and Immunology, Research Institute, National Centre for Global Health and Medicine, Chiba, Japan.
Yuki I KawamuraDepartment of Gastroenterology, Research Centre for Hepatitis and Immunology, Research Institute, National Centre for Global Health and Medicine, Chiba, Japan.
Taeko DohiDepartment of Gastroenterology, Research Centre for Hepatitis and Immunology, Research Institute, National Centre for Global Health and Medicine, Chiba, Japan.
Kenshiro OshimaDepartment of Computational Biology and Medical Sciences, Graduate School of Frontier Science, The University of Tokyo, Chiba, Japan.
Masahira HattoriDepartment of Computational Biology and Medical Sciences, Graduate School of Frontier Science, The University of Tokyo, Chiba, Japan.
Susumu NakaeLaboratory of Systems Biology, Centre for Experimental Medicine and Systems Biology, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Kiyoshi TakatsuDepartment of Gastroenterology, Research Centre for Hepatitis and Immunology, Research Institute, National Centre for Global Health and Medicine, Chiba, Japan.
Satoshi TakakiDepartment of Immune Regulation, Research Centre for Hepatitis and Immunology, Research Institute, National Centre for Global Health and Medicine, Chiba, Japan.
National Center for Global Health and Medicine · JPThe University of Tokyo · JPJapan Science and Technology Agency · JPUniversity of Toyama · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Group 2 innate lymphoid cells (ILC2s) produce a significant amount of interleukin-5 (IL-5), which supports eosinophil responses in various tissues; they also produce IL-13, which induces mucus production and contributes to tissue repair or fibrosis. The ILC2s are activated by alarmins, such as IL-33 released from epithelia, macrophages and natural killer T (NKT) cells in response to infection and allergen exposure, leading to epithelial injury. We examined gene expression in lung ILC2s and found that ILC2s expressed Ifngr1, the receptor for interferon-γ (IFN-γ). Interferon-γ severely inhibited IL-5 and IL-13 production by lung and kidney ILC2s. To evaluate the effects in vivo, we used α-galactosylceramide (α-GalCer) to induce NKT cells to produce IL-33 and IFN-γ. Intraperitoneal injection of α-GalCer in mice induced NKT cell activation resulting in IL-5 and IL-13 production by ILC2s. Administration of anti-IFN-γ together with α-GalCer significantly enhanced the production of IL-5 and IL-13 by ILC2s in lung and kidney. Conversely, cytokine production from ILC2s was markedly suppressed after injection of exogenous IL-33 in Il33(-/-) mice pre-treated with α-GalCer. Hence, IFN-γ induced or already present in tissues can impact downstream pleiotropic functions mediated by ILC2s, such as inflammation and tissue repair.

Indexed as

AnimalsCells, CulturedGalactosylceramidesImmunity, InnateInterferon-gammaInterferon gamma ReceptorInterleukin-13Interleukin-33Interleukin-5KidneyLungLymphocyte ActivationLymphocytesMice, Inbred C57BLMice, TransgenicNatural Killer T-Cellsalpha-galactosylceramideGalactosylceramidesIl33 protein, mouseInterferon-gammaInterferon gamma ReceptorInterleukin-13Interleukin-33Interleukin-5Receptors, Interferongroup 2 innate lymphoid cellsinterferon-γinterleukin-13interleukin-5T helper type 2 cytokines

Identifiers

PMID26425820
PMCPMC4693881
OpenAlexW2155528991

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.