Evidence map›Paper›PMID 25505948›Full record

ArticleClinical & translational immunology2013

IL-21 Modulates Activation of NKT Cells in Patients with Stage IV Malignant Melanoma.

Jonathan M Coquet, Kresten Skak, Ian D Davis, Mark J Smyth, Dale I Godfrey

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Clinical & translational immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00336986 (An Open-label, Dose Escalation Safety and Tolerability Study of Recombinant Human Interleukin-21), which is not on this map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 29% 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.

NCT00336986 phase2completednot on this map

An Open-label, Dose Escalation Safety and Tolerability Study of Recombinant Human Interleukin-21 (Phase 1) Followed by an Open-label Treatment Study (Phase 2a) in Patients With Stage IV Malignant Melanoma

TypeinterventionalSponsorNovo Nordisk A/SRan2004 to 2007Enrolled54ConditionsCancer, Malignant MelanomaArmsrecombinant interleukin-21
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. IL-21 Selectively Protects CD62LJournal of immunology (Baltimore, Md. : 1950) · 2018
    Article
  11. Review
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 4 institutions in 2 countries.

Jonathan M CoquetDepartment of Microbiology and Immunology, University of Melbourne , Parkville, Victoria, Australia.
Kresten SkakDepartment of Histology and Cancer Pharmacology, Novo Nordisk A/S , Maalov, Denmark.
Ian D DavisLudwig Institute for Cancer Research, Austin Health , Melbourne, Victoria, Australia.
Mark J SmythCancer Immunology Program, Peter MacCallum Cancer Centre , East Melbourne, Victoria, Australia ; Immunology in Cancer and Infection Laboratory, Queensland Institute of Medical Research , Herston, Queensland, Australia ; School of Medicine, University of Queensland , Herston, Queensland, Australia.
Dale I GodfreyDepartment of Microbiology and Immunology, University of Melbourne , Parkville, Victoria, Australia.
University of Melbourne · AUAustin Health · AUNovo Nordisk (Denmark) · DKQIMR Berghofer Medical Research Institute · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin-21 (IL-21) is a common γ-chain cytokine produced by T helper and natural killer T (NKT) cells. It has been shown to regulate the response of various lymphocyte subsets including NK, NKT, T and B cells. Owing to its potent anti-tumor function in preclinical studies and its ability to induce cytotoxicity and interferon-γ (IFN-γ) production in NK and CD8 T cells, recombinant IL-21 (rIL-21) was fast-tracked into early-phase clinical trials of patients with various malignancies. In a phase 2a trial of patients with metastatic melanoma, we analyzed the frequency and function of NKT cells in patients receiving rIL-21. NKT cells were present at a low frequency, but their levels were relatively stable in patients administered rIL-21. Unlike our observations in NK and CD8 T cells, rIL-21 appeared to reduce IFN-γ and TNF production by NKT cells, whereas it enhanced IL-4 production. It also modulated the expression of cell surface markers, specifically on CD4(-) NKT cells. In addition, an increase in CD3(+)CD56(+) NKT-like cells was observed over the course of rIL-21 administration. These results highlight that IL-21 is a potent regulator of NKT cell function in vivo.

Indexed as

CancerIL-21NKTT helper

Identifiers

PMID25505948
PMCPMC4232058
OpenAlexW2041628018

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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.