Evidence map›Paper›PMID 16621986›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2006

Immunological and antitumor effects of IL-23 as a cancer vaccine adjuvant.

Willem W Overwijk, Karin E de Visser, Felicia H Tirion, Laurina A de Jong, Thijs W H Pols, Yme U van der Velden, Jasper G van den Boorn, Anna M Keller, Wim A Buurman, Marc R Theoret and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

38 citing papers in PubMed, 80 citations in OpenAlex.

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  7. Dendritic Cells in Irradiated Mice Trigger the Functional Plasticity and Antitumor Activity of Adoptively Transferred Tc17 Cells via IL12 Signaling.Clinical cancer research : an official journal of the American Association for Cancer Research · 2015
    Article
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  16. Dendritic cell-based vaccines: barriers and opportunities.Future oncology (London, England) · 2012
    Review
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  18. Article
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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

15 authors at 4 institutions in 2 countries.

Willem W OverwijkDivision of Immunology, The Netherlands Cancer Institute, 1105 AZ Amsterdam, The Netherlands. woverwijk@mdanderson.org
Karin E de Visser
Felicia H Tirion
Laurina A de Jong
Thijs W H Pols
Yme U van der Velden
Jasper G van den Boorn
Anna M Keller
Wim A Buurman
Marc R Theoret
Bianca Blom
Nicholas P Restifo
Ada M Kruisbeek
Robert A Kastelein
John B A G Haanen
The Netherlands Cancer Institute · NLNational Institutes of Health · USMaastricht University · NLPalo Alto Research Center · US

Funding

Building on the success of the adoptive immunotherapy of cancerZ01BC010763 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI RESTIFO, NICHOLAS P · 2006 to 2008
$6.4M
RECOMBINANT AND SYNTHETIC ANTI-CANCER VACCINESZ01SC006670 · SC · CLINICAL SCIENCES · PI RESTIFO, NICHOLAS P · 1996 to 2005
–
Intramural NIH HHS Z01 BC010763Intramural NIH HHS Z99 CA999999
6 · The paper itself

Abstract

The promising, but modest, clinical results of many human cancer vaccines indicate a need for vaccine adjuvants that can increase both the quantity and the quality of vaccine-induced, tumor-specific T cells. In this study we tested the immunological and antitumor effects of the proinflammatory cytokine, IL-23, in gp100 peptide vaccine therapy of established murine melanoma. Neither systemic nor local IL-23 alone had any impact on tumor growth or tumor-specific T cell numbers. Upon specific vaccination, however, systemic IL-23 greatly increased the relative and absolute numbers of vaccine-induced CD8(+) T cells and enhanced their effector function at the tumor site. Although IL-23 specifically increased IFN-gamma production by tumor-specific T cells, IFN-gamma itself was not a primary mediator of the vaccine adjuvant effect. The IL-23-induced antitumor effect and accompanying reversible weight loss were both partially mediated by TNF-alpha. In contrast, local expression of IL-23 at the tumor site maintained antitumor activity in the absence of weight loss. Under these conditions, it was also clear that enhanced effector function of vaccine-induced CD8(+) T cells, rather than increased T cell number, is a primary mechanism underlying the antitumor effect of IL-23. Collectively, these results suggest that IL-23 is a potent vaccine adjuvant for the induction of therapeutic, tumor-specific CD8(+) T cell responses.

Indexed as

Adjuvants, ImmunologicAnimalsAntigensAntineoplastic AgentsCancer VaccinesCD8-Positive T-LymphocytesCell ProliferationCells, CulturedInterferon-gammaInterleukin-23Interleukin-23 Subunit p19InterleukinsMiceTime FactorsTumor Necrosis Factor-alphaWeight LossAdjuvants, ImmunologicAntigensAntineoplastic AgentsCancer VaccinesIL23A protein, humanIl23a protein, mouseInterferon-gammaInterleukin-23Interleukin-23 Subunit p19InterleukinsTumor Necrosis Factor-alpha

Identifiers

PMID16621986
PMCPMC2242845
OpenAlexW2137450012

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.