Evidence map›Paper›PMID 29296539›Full record

ArticleOncoimmunology

Interleukin-21 combined with PD-1 or CTLA-4 blockade enhances antitumor immunity in mouse tumor models.

Katherine E Lewis, Mark J Selby, Gregg Masters, Jose Valle, Gennaro Dito, Wendy R Curtis, Richard Garcia, Kathy A Mink, Kimberly S Waggie, Matthew S Holdren and 4 more

Abstract read
In one paragraph

Article in Oncoimmunology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed.

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  15. Biological Insight and Recent Advancement in the Treatment of Neuroblastoma.International journal of molecular sciences · 2023
    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

14 authors.

Katherine E LewisOncology Discovery Research, Bristol-Myers Squibb, Seattle, WA.
Mark J SelbyOncology Discovery Research, Bristol-Myers Squibb, Redwood City, CA.
Gregg MastersOncology Translational Research, Bristol-Myers Squibb, Princeton, NJ.
Jose ValleOncology Discovery Research, Bristol-Myers Squibb, Redwood City, CA.
Gennaro DitoOncology Translational Research, Bristol-Myers Squibb, Princeton, NJ.
Wendy R CurtisOncology Discovery Research, Bristol-Myers Squibb, Seattle, WA.
Richard GarciaOncology Discovery Research, Bristol-Myers Squibb, Seattle, WA.
Kathy A MinkOncology Discovery Research, Bristol-Myers Squibb, Seattle, WA.
Kimberly S WaggieOncology Discovery Research, Bristol-Myers Squibb, Seattle, WA.
Matthew S HoldrenDrug Safety Evaluation, Bristol-Myers Squibb, Mt. Vernon, IN.
Joseph F GrossoEarly Clinical Development, Bristol-Myers Squibb, Princeton, NJ.
Alan J KormanOncology Discovery Research, Bristol-Myers Squibb, Redwood City, CA.
Maria Jure-KunkelOncology Translational Research, Bristol-Myers Squibb, Princeton, NJ.
Stacey R DillonOncology Discovery Research, Bristol-Myers Squibb, Seattle, WA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent advances in cancer treatment with checkpoint blockade of receptors such as CTLA-4 and PD-1 have demonstrated that combinations of agents with complementary immunomodulatory effects have the potential to enhance antitumor activity as compared to single agents. We investigated the efficacy of immune-modulatory interleukin-21 (IL-21) combined with checkpoint blockade in several syngeneic mouse tumor models. After tumor establishment, mice were administered recombinant mouse IL-21 (mIL-21) alone or in combination with blocking monoclonal antibodies against mouse PD-1 or CTLA-4. In contrast to monotherapy, IL-21 enhanced antitumor activity of mCTLA-4 mAb in four models and anti-PD-1 mAb in two models, with evidence of synergy for one or both of the combination treatments in the EMT-6 and MC38 models. The enhanced efficacy was associated with increased intratumoral CD8+ T cell infiltrates, CD8+ T cell proliferation, and increased effector memory T cells, along with decreased frequency of central memory CD8+ T cells.

Indexed as

B16-F10CT26CTLA-4EMT-6IL-21interleukin 21MC38mouse tumor modelsPD-1

Identifiers

PMID29296539
PMCPMC5739581

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.