Evidence map›Paper›PMID 31856922›Full record

ArticleJournal for immunotherapy of cancer2019

Interleukin-15 in cancer immunotherapy: IL-15 receptor complex versus soluble IL-15 in a cancer cell-delivered murine leukemia model.

Alexandra Berger, Sarah J Colpitts, Melanie S S Seabrook, Caren L Furlonger, Maura B Bendix, Joshua M Moreau, William M McKillop, Jeffrey A Medin, Christopher J Paige

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
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  4. Review
  5. Article
  6. Engineered murine IL-21-secreting leukemia cells induce granzyme BCancer immunology, immunotherapy : CII · 2023
    Article
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  10. 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

9 authors at 1 institution in 2 countries.

Alexandra BergerPrincess Margaret Cancer Centre, University Health Network, 610 University Avenue, Room 8-105, Toronto, Ontario, M5G 2M9, Canada. aberger@uhnres.utoronto.ca.ORCID 0000-0002-6044-6616
Sarah J ColpittsPrincess Margaret Cancer Centre, University Health Network, 610 University Avenue, Room 8-105, Toronto, Ontario, M5G 2M9, Canada.
Melanie S S SeabrookPrincess Margaret Cancer Centre, University Health Network, 610 University Avenue, Room 8-105, Toronto, Ontario, M5G 2M9, Canada.
Caren L FurlongerPrincess Margaret Cancer Centre, University Health Network, 610 University Avenue, Room 8-105, Toronto, Ontario, M5G 2M9, Canada.
Maura B BendixPrincess Margaret Cancer Centre, University Health Network, 610 University Avenue, Room 8-105, Toronto, Ontario, M5G 2M9, Canada.
Joshua M MoreauPrincess Margaret Cancer Centre, University Health Network, 610 University Avenue, Room 8-105, Toronto, Ontario, M5G 2M9, Canada.
William M McKillopPrincess Margaret Cancer Centre, University Health Network, 610 University Avenue, Room 8-105, Toronto, Ontario, M5G 2M9, Canada.
Jeffrey A MedinPrincess Margaret Cancer Centre, University Health Network, 610 University Avenue, Room 8-105, Toronto, Ontario, M5G 2M9, Canada.
Christopher J PaigePrincess Margaret Cancer Centre, University Health Network, 610 University Avenue, Room 8-105, Toronto, Ontario, M5G 2M9, Canada.
University Health Network · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytokines of the common γ-chain receptor family such as IL-15 are vital with respect to activating immune cells, sustaining healthy immune functions, and augmenting the anti-tumor activity of effector cells, making them ideal candidates for cancer immunotherapy. IL-15, either in its soluble form (IL-15sol) or complexed with IL-15Rα (IL-15Rc), has been shown to exhibit potent anti-tumor activities in various experimental cancer studies. Here we describe the impact of intraperitoneal IL-15 in a cancer cell-delivered IL-15 immunotherapy approach using the 70Z/3-L leukemia mouse model. Whereas both forms of IL-15 led to significantly improved survival rates compared to the parent cell line, there were striking differences in the extent of the improved survival: mice receiving cancer cells secreting IL-15sol showed significantly longer survival and protective long-term immunity compared to those producing IL-15Rc. Interestingly, injection of leukemia cells secreting IL-15sol lead to heightened expansion of CD4

Indexed as

ImmunomodulationImmunotherapyAnimalsCell Line, TumorCytokinesDisease Models, AnimalFemaleGene ExpressionHumansInterleukin-15Killer Cells, NaturalLeukemiaMelanoma, ExperimentalMiceProtein BindingReceptors, Interleukin-15CytokinesInterleukin-15Receptors, Interleukin-15Cancer immunotherapyInterleukin-15LeukemiaNK-cellsT-cells

Identifiers

PMID31856922
PMCPMC6924073
OpenAlexW2995191565

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.