Evidence map›Paper›PMID 24982172›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

IL-33/ST2 axis promotes mast cell survival via BCLXL.

Jun-Xia Wang, Shinjiro Kaieda, Sarah Ameri, Nadia Fishgal, Daniel Dwyer, Anthony Dellinger, Christopher L Kepley, Michael F Gurish, Peter A Nigrovic

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

49 citing papers in PubMed, 83 citations in OpenAlex.

  1. CD25 expression marks an activated mast cell population in human nasal polyposis.The Journal of allergy and clinical immunology · 2026
    Article
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  5. Targeting alarmins in asthma: From bench to clinic.The Journal of allergy and clinical immunology · 2025
    Review
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  7. Article
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  13. Discovery of highly immunogenic spleen-resident FCGR3Cellular & molecular immunology · 2023
    Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. IL-33 mediates Pseudomonas induced airway fibrogenesis and is associated with CLAD.The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2023
    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

9 authors at 3 institutions in 2 countries.

Jun-Xia WangDivision of Rheumatology, Immunology, and Allergy, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115;
Shinjiro KaiedaDivision of Rheumatology, Immunology, and Allergy, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115;Department of Medicine, Kurume University School of Medicine, Kurume 830-0011, Japan;
Sarah AmeriDivision of Rheumatology, Immunology, and Allergy, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115;
Nadia FishgalDivision of Rheumatology, Immunology, and Allergy, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115;
Daniel DwyerDivision of Rheumatology, Immunology, and Allergy, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115;
Anthony DellingerDepartment of Nanoscience, Joint School of Nanoscience and Nanotechnology, University of North Carolina at Greensboro, Greensboro, NC 27412; and.
Christopher L KepleyDepartment of Nanoscience, Joint School of Nanoscience and Nanotechnology, University of North Carolina at Greensboro, Greensboro, NC 27412; and.
Michael F GurishDivision of Rheumatology, Immunology, and Allergy, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115;
Peter A NigrovicDivision of Rheumatology, Immunology, and Allergy, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115;Division of Immunology, Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115 pnigrovic@partners.org.
Brigham and Women's Hospital · USHarvard University · USUniversity of North Carolina at Greensboro · US

Funding

C5a receptor on mast cells in inflammatory arthritisK08AR051321 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI NIGROVIC, PETER A · 2006 to 2010
$643k
Pro-inflammatory role of megakaryocytes in arthritisR21AR062328 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI NIGROVIC, PETER A · 2012 to 2013
$413k
NIAMS NIH HHS AR051321NIAMS NIH HHS AR062328NIAMS NIH HHS K08 AR051321NIAMS NIH HHS R21 AR062328
6 · The paper itself

Abstract

Mast cells (MC) are potent innate immune cells that accumulate in chronically inflamed tissues. MC express the IL-33 receptor IL-1 receptor-related protein ST2 at high level, and this IL-1 family cytokine both activates MC directly and primes them to respond to other proinflammatory signals. Whether IL-33 and ST2 play a role in MC survival remains to be defined. In skin-derived human MC, we found that IL-33 attenuated MC apoptosis without altering proliferation, an effect mediated principally through the antiapoptotic molecule B-cell lymphoma-X large (BCLXL). Murine MC demonstrated a similar mechanism, dependent entirely on ST2. In line with these observations, St2(-/-) mice exhibited reduced numbers of tissue MC in inflamed arthritic joints, in helminth-infected intestine, and in normal peritoneum. To confirm an MC-intrinsic role for ST2 in vivo, we performed peritoneal transfer of WT and St2(-/-) MC. In St2(-/-) hosts treated with IL-33 and in WT hosts subjected to thioglycollate peritonitis, WT MC displayed a clear survival advantage over coengrafted St2(-/-) MC. IL-33 blockade specifically attenuated this survival advantage, confirming IL-33 as the relevant ST2 ligand mediating MC survival in vivo. Together, these data reveal a cell-intrinsic role for the IL-33/ST2 axis in the regulation of apoptosis in MC, identifying thereby a previously unappreciated pathway supporting expansion of the MC population with inflammation.

Indexed as

AnimalsArthritisbcl-X ProteinCell SurvivalHelminthiasisHumansInflammationInterleukin-1 Receptor-Like 1 ProteinInterleukin-33InterleukinsIntestinal MucosaIntestinesJointsMast CellsMiceMice, KnockoutBCL2L1 protein, humanBcl2l1 protein, mousebcl-X ProteinIL1RL1 protein, humanIl1rl1 protein, mouseIL33 protein, humanIl33 protein, mouseInterleukin-1 Receptor-Like 1 ProteinInterleukin-33InterleukinsReceptors, Cell SurfaceReceptors, Interleukinarthritishelminth infection

Identifiers

PMID24982172
PMCPMC4104908
OpenAlexW2035585307

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.