Evidence map›Paper›PMID 25000978›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

Increased antitumor effects using IL-2 with anti-TGF-β reveals competition between mouse NK and CD8 T cells.

Maite Alvarez, Myriam N Bouchlaka, Gail D Sckisel, Can M Sungur, Mingyi Chen, William J Murphy

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. TGF-β Regulation of T Cells.Annual review of immunology · 2023
    Review
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  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
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  15. Review
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  18. Review
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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

6 authors.

Maite AlvarezDepartment of Dermatology, University of California, Davis, Sacramento, CA 95817;
Myriam N BouchlakaDepartment of Microbiology and Immunology, University of Nevada, Reno, Reno, NV 89557;
Gail D SckiselDepartment of Dermatology, University of California, Davis, Sacramento, CA 95817;
Can M SungurDepartment of Dermatology, University of California, Davis, Sacramento, CA 95817;
Mingyi ChenDepartment of Pathology and Laboratory Medicine, University of California, Davis, Sacramento, CA 95817; and.
William J MurphyDepartment of Dermatology, University of California, Davis, Sacramento, CA 95817; Department of Internal Medicine, University of California, Davis, Sacramento, CA 95817 wmjmurphy@ucdavis.edu.

Funding

Positive and Negative Regulation of Natural Killer Cells After BMTR01HL089905 · NHLBI · UNIVERSITY OF NEVADA RENO · PI MURPHY, WILLIAM JOSEPH · 2007 to 2015
$3.1M
NHLBI NIH HHS R01 HL089905NHLBI NIH HHS R01-HL089905
6 · The paper itself

Abstract

Because of increasing interest in the removal of immunosuppressive pathways in cancer, the combination of IL-2 with Abs to neutralize TGF-β, a potent immunosuppressive cytokine, was assessed. Combination immunotherapy resulted in significantly greater antitumor effects. These were correlated with significant increases in the numbers and functionality of NK cells, NK cell progenitors, and activated CD8 T cells, resulting in the observed antitumor effects. Combination immunotherapy also was accompanied by lesser toxicities than was IL-2 therapy alone. Additionally, we observed a dual competition between NK cells and activated CD8 T cells such that, after immunotherapy, the depletion of either effector population resulted in the increased total expansion of the other population and compensatory antitumor effects. This study demonstrates the efficacy of this combination immunotherapeutic regimen as a promising cancer therapy and illustrates the existence of potent competitive regulatory pathways between NK cells and CD8 T cells in response to systemic activation.

Indexed as

AnimalsAntibodies, NeutralizingCD8-Positive T-LymphocytesCell Line, TumorFas Ligand Proteinfas ReceptorFemaleImmunotherapyInterleukin-2Killer Cells, NaturalLymphocyte ActivationMiceMice, Inbred C57BLMice, KnockoutNeoplasmsNK Cell Lectin-Like Receptor Subfamily AAntibodies, NeutralizingFas Ligand ProteinFasl protein, mousefas ReceptorInterleukin-2Klra7 protein, mouseKlrk1 protein, mouseNK Cell Lectin-Like Receptor Subfamily ANK Cell Lectin-Like Receptor Subfamily CNK Cell Lectin-Like Receptor Subfamily KTransforming Growth Factor beta

Identifiers

PMID25000978
PMCPMC4241855

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.