Evidence map›Paper›PMID 16612597›Full record

ArticleCancer immunology, immunotherapy : CII2007

Effects of interferon gamma on native human acute myelogenous leukaemia cells.

Elisabeth Ersvaer, Jørn Skavland, Elling Ulvestad, Bjørn Tore Gjertsen, Øystein Bruserud

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

15 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Th1 cytokines in pediatric acute lymphoblastic leukemia.Cancer immunology, immunotherapy : CII · 2023
    Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Allogeneic Human Double Negative T Cells as a Novel Immunotherapy for Acute Myeloid Leukemia and Its Underlying Mechanisms.Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. 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

5 authors at 2 institutions in 1 country.

Elisabeth ErsvaerInstitute of Medicine, Section for Hematology, The University of Bergen and Haukeland University Hospital, Bergen, Norway. elisabeth.ersvar@med.uib.no
Jørn Skavland
Elling Ulvestad
Bjørn Tore Gjertsen
Øystein Bruserud
Haukeland University Hospital · NOUniversity of Bergen · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T cell targeting immunotherapy is now considered a possible strategy in acute myelogenous leukaemia (AML), and IFNgamma release may then contribute to the antileukaemic effects. We investigated the effects of IFNgamma on native human AML cells. Normal T cells could be activated to release IFNgamma in the presence of AML cells. Furthermore, high levels of CD119 (IFNgamma receptor alpha chain) expression were observed for all 39 patients examined. Receptor expression was decreased after exposure to exogenous IFNgamma, and receptor ligation caused Stat1 phosphorylation but no phosphorylation of the alternative messengers Erk1/2. The effect of exogenous IFNgamma on AML blast proliferation was dependent on the local cytokine network and IFNgamma (1) inhibited proliferation in the presence of exogenous IL1beta, GM-CSF, G-CSF and SCF; (2) had divergent effects in the presence of IL3 and Flt3 (65 patients examined); (3) inhibited proliferation in the presence of endothelial cells but had divergent effects in the presence of fibroblasts, osteoblasts and normal stromal cells (65 patients examined). IFNgamma increased stress-induced (spontaneous) in vitro apoptosis as well as cytarabine-induced apoptosis only for a subset of patients. Furthermore, IFNgamma decreased the release of proangiogenic CXCL8 and increased the release of antiangiogenic CXCL9-11. We conclude that IFNgamma can be released in the presence of native human AML cells and affect AML cell proliferation, regulation of apoptosis and the balance between pro- and antiangiogenic chemokine release.

Indexed as

Cell ProliferationSignal TransductionAdultAgedAged, 80 and overApoptosisChemokine CXCL9Chemokines, CXCCytarabineEndothelium, VascularFemaleFibroblastsFlow Cytometryfms-Like Tyrosine Kinase 3Granulocyte Colony-Stimulating FactorGranulocyte-Macrophage Colony-Stimulating FactorChemokine CXCL9Chemokines, CXCCXCL8 protein, humanCXCL9 protein, humanCytarabineFLT3 protein, humanfms-Like Tyrosine Kinase 3Granulocyte Colony-Stimulating FactorGranulocyte-Macrophage Colony-Stimulating FactorInterferon-gammaInterferon gamma ReceptorInterleukin-1betaInterleukin-3Interleukin-8Mitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Receptors, InterferonSTAT1 protein, humanSTAT1 Transcription Factor

Identifiers

PMID16612597
PMCPMC11030278
OpenAlexW2050752215

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.