Evidence map›Paper›PMID 25676709›Full record

ArticleCancer immunology, immunotherapy : CII2015

Interleukin-12 enhances the function and anti-tumor activity in murine and human CD8(+) T cells.

Mark P Rubinstein, Ee Wern Su, Samantha Suriano, Colleen A Cloud, Kristina Andrijauskaite, Pravin Kesarwani, Kristina M Schwartz, Katelyn M Williams, C Bryce Johnson, Mingli Li and 6 more

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

25 citing papers in PubMed, 44 citations in OpenAlex.

  1. Renaissance of antiviral CD8Nature reviews. Immunology · 2026
    Review
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  3. Article
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  5. Article
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  7. Article
  8. Article
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  10. Article
  11. Brief in vitro IL-12 conditioning of CD8Cancer immunology, immunotherapy : CII · 2021
    Review
  12. Article
  13. Review
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  15. Review
  16. Article
  17. Review
  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

16 authors at 3 institutions in 2 countries.

Mark P RubinsteinDepartment of Surgery, Medical University of South Carolina, 86 Jonathan Lucas Street, HO506, Charleston, SC, 29425, USA, markrubinstein@musc.edu.
Ee Wern Su
Samantha Suriano
Colleen A Cloud
Kristina Andrijauskaite
Pravin Kesarwani
Kristina M Schwartz
Katelyn M Williams
C Bryce Johnson
Mingli Li
Gina M Scurti
Mohamed L Salem
Chrystal M Paulos
Elizabeth Garrett-Mayer
Shikhar Mehrotra
David J Cole
Medical University of South Carolina · USLoyola University Chicago · USTanta University · EG

Funding

Translational Science Laboratory Shared ResourceP30CA138313 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RAYMOND N. DUBOIS · 2009 to 2026
$42.7M
TCR TRANSDUCED CDB T CELLS FOR ADOPTIVE IMMUNOTHERAPYP01CA154778 · NCI · LOYOLA UNIVERSITY CHICAGO · PI NISHIMURA, MICHAEL I. · 2011 to 2015
$15.4M
Costimulatory mechanisms of antitumor Th17 cell immunityR01CA175061 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI PAULOS, CHRYSTAL MARY · 2013 to 2017
$1.5M
Oxidative stress and AICD in memory T cell persistenceR01CA138930 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MEHROTRA, SHIKHAR · 2010 to 2014
$1.5M
Maximizing Memory T Cell Responses by Matured Post Chemotherapy Dendritic CellsR01CA133503 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RUBINSTEIN, MARK P · 2010 to 2012
$900k
Improving Adoptive T cell Therapy with ex vivo IL-12 Priming and LymphodepletionF30CA177208 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI JOHNSON, CHRISTOPHER BRYCE · 2013 to 2016
$156k
NCI NIH HHS F30 CA177208NCI NIH HHS P01 CA154778NCI NIH HHS P01CA54778-01NCI NIH HHS P30 CA138313NCI NIH HHS P30CA138313NCI NIH HHS R01 CA133503NCI NIH HHS R01CA133503NCI NIH HHS R01 CA138930NCI NIH HHS R01CA138930NCI NIH HHS R01 CA175061NCI NIH HHS R01CA175061
6 · The paper itself

Abstract

Mouse CD8(+) T cells conditioned with interleukin (IL)-12 ex vivo mediate the potent regression of established melanoma when transferred into lymphodepleted mice. However, the quantitative and qualitative changes induced by IL-12 in the responding mouse CD8(+) T cells have not been well defined. Moreover, the mechanisms by which IL-12-conditioning impacts human CD8(+) T cells, and how such cells might be expanded prior to infusion into patients is not known. We found that ex vivo IL-12-conditioning of mouse CD8(+) T cells led to a tenfold-100-fold increase in persistence and anti-tumor efficacy upon adoptive transfer into lymphodepleted mice. The enhancing effect of IL-12 was associated with maintenance of functional avidity. Importantly, in the context of ongoing ACT clinical trials, human CD8(+) T cells genetically modified with a tyrosinase-specific T cell receptor (TCR) exhibited significantly enhanced functional activity when conditioned with IL-12 as indicated by heightened granzyme B expression and elevated peptide-specific CD107a degranulation. This effect was sustainable despite the 20 days of in vitro cellular expansion required to expand cells over 1,000-fold allowing adequate cell numbers for administration to cancer patients. Overall, these findings support the efficacy and feasibility of ex vivo IL-12-conditioning of TCR-modified human CD8(+) T cells for adoptive transfer and cancer therapy.

Indexed as

Adoptive TransferAnimalsCD8-Positive T-LymphocytesCell Line, TumorCell ProliferationGranzymesHumansInterleukin-12Lymphocyte DepletionLysosomal-Associated Membrane Protein 1MelanomaMiceMice, Inbred C57BLMice, KnockoutReceptors, Antigen, T-CellSkin NeoplasmsGranzymesInterleukin-12Lysosomal-Associated Membrane Protein 1Receptors, Antigen, T-Cell

Identifiers

PMID25676709
PMCPMC4804872
OpenAlexW2015874075

What OpenQuestion holds

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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.