Evidence map›Paper›PMID 25297635›Full record

ArticleCancer research2014

Inhibition of adaptive immunity by IL9 can be disrupted to achieve rapid T-cell sensitization and rejection of progressive tumor challenges.

Dominique B Hoelzinger, Ana Lucia Dominguez, Peter A Cohen, Sandra J Gendler

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

31 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. T cells in health and disease.Signal transduction and targeted therapy · 2023
    Review
  6. The Dichotomy of Interleukin-9 Function in the Tumor Microenvironment.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2023
    Review
  7. Review
  8. Article
  9. Review
  10. The Role ofCells · 2021
    Article
  11. Review
  12. Interleukin-9 in Immunopathology ofFrontiers in cellular and infection microbiology · 2021
    Article
  13. Targeting the IL-9 pathway in cancer immunotherapy.Human vaccines & immunotherapeutics · 2020
    Review
  14. The Role of Interleukin-9 in Cancer.Pathology oncology research : POR · 2020
    Review
  15. Article
  16. IL-9 and IL-9-producing cells in tumor immunity.Cell communication and signaling : CCS · 2020
    Review
  17. Article
  18. The dichotomous function of interleukin-9 in cancer diseases.Journal of molecular medicine (Berlin, Germany) · 2019
    Review
  19. Review
  20. 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

4 authors at 1 institution in 1 country.

Dominique B HoelzingerDepartment of Immunology, Mayo Clinic College of Medicine, Mayo Clinic, Scottsdale, Arizona. hoelzinger.dominique@mayo.edu.
Ana Lucia DominguezDepartment of Immunology, Mayo Clinic College of Medicine, Mayo Clinic, Scottsdale, Arizona.
Peter A CohenDepartment of Immunology, Mayo Clinic College of Medicine, Mayo Clinic, Scottsdale, Arizona. Department of Hematology/Oncology, Mayo Clinic College of Medicine, Mayo Clinic, Scottsdale, Arizona.
Sandra J GendlerDepartment of Immunology, Mayo Clinic College of Medicine, Mayo Clinic, Scottsdale, Arizona. Department of Hematology/Oncology, Mayo Clinic College of Medicine, Mayo Clinic, Scottsdale, Arizona. Department of Biochemistry and Molecular Biology, Mayo Clinic College of Medicine, Mayo Clinic, Scottsdale, Arizona.
Mayo Clinic in Arizona · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Felicity Enders · 1985 to 2026
$151.3M
Tissue CoreP50CA102701 · NCI · MAYO CLINIC ROCHESTER · PI PETERSEN, GLORIA M. · 2004 to 2018
$32.7M
Role of IL-9 in Treg Biology and Tumor ImmunityR01CA155295 · NCI · MAYO CLINIC ARIZONA · PI GENDLER, SANDRA J · 2011 to 2015
$1.7M
NCI NIH HHS 5P50 CA102701NCI NIH HHS CA155295-01-03ANCI NIH HHS P30 CA015083NCI NIH HHS P50 CA102701NCI NIH HHS R01 CA155295PHS HHS R01A108984
6 · The paper itself

Abstract

The tolerogenic cytokine IL9 promotes T regulatory cell function and allergic airway inflammation, but it has not been extensively studied in cancer. In this report, we used IL9-deficient mice to investigate the effects of IL9 in multiple models of breast and colon cancer development. Eliminating endogenous IL9 enabled sensitization of host T cells to tumors, leading to their early rejection without the requirement of vaccines or immunomodulatory therapies. Notably, IL9-deficient mice acquired immunologic memory, which actively protected from residual disease and tumor rechallenge, an effect linked to activation of CD8(+) T cells. Depletion of either CD8(+) or CD4(+) T cells abolished the benefits of IL9 loss to tumor control. Adoptive transfer experiments showed that T cells from tumor-rejecting IL9-deficient mice retained their effector competency in wild-type animals. Moreover, neutralizing IL9 antibody phenocopied the effects of IL9 gene deletion by slowing tumor progression in wild-type animals. Our results show the ability of IL9 to function as an inhibitor of adaptive immunity that prevents the formation of immunologic memory to a growing tumor, highlighting the potential for IL9 neutralization as a unique tool for cancer immunotherapy.

Indexed as

Adaptive ImmunityAnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesFemaleImmunologic MemoryImmunotherapy, AdoptiveInterleukin-9Lymphocyte ActivationMaleMiceMice, Inbred BALB CMice, TransgenicInterleukin-9

Identifiers

PMID25297635
PMCPMC4254354
OpenAlexW1993991182

What OpenQuestion holds

Textmetadata
LicenceTDM
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.