Evidence map›Paper›PMID 25143233›Full record

ArticleCancer immunology, immunotherapy : CII2014

CpG-mediated modulation of MDSC contributes to the efficacy of Ad5-TRAIL therapy against renal cell carcinoma.

Britnie R James, Kristin G Anderson, Erik L Brincks, Tamara A Kucaba, Lyse A Norian, David Masopust, Thomas S Griffith

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

26 citing papers in PubMed, 37 citations in OpenAlex.

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  13. Dietary Protein Restriction Reprograms Tumor-Associated Macrophages and Enhances Immunotherapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
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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

7 authors at 2 institutions in 1 country.

Britnie R JamesDepartment of Urology, University of Minnesota, 3-125 CCRB, 2231 6th St. SE, Minneapolis, MN, 55455, USA.
Kristin G Anderson
Erik L Brincks
Tamara A Kucaba
Lyse A Norian
David Masopust
Thomas S Griffith
University of Minnesota · USUniversity of Iowa · US

Funding

Mucosal T Cell Memory to PathogensR01AI084913 · NIAID · UNIVERSITY OF MINNESOTA · PI MASOPUST, DAVID · 2010 to 2023
$5.8M
Minnesota Craniofacial Research Training ProgramT90DE022732 · NIDCR · UNIVERSITY OF MINNESOTA · PI MANSKY, KIM CARPENTER · 2012 to 2023
$4.9M
TRAIL-expressing Recombinant Adenovirus Based Immunotherapy for RCCR01CA109446 · NCI · UNIVERSITY OF MINNESOTA · PI GRIFFITH, THOMAS S · 2004 to 2013
$2.6M
Mucosal T cell memory to pathogensR37AI084913 · NIAID · UNIVERSITY OF MINNESOTA · PI DAVID MASOPUST · 2024 to 2026
$1.7M
Obesity Affects Immunity to Kidney CancerR01CA181088 · NCI · UNIVERSITY OF IOWA · PI NORIAN, LYSE A · 2014 to 2018
$1.5M
NCI NIH HHS CA109446NCI NIH HHS R01 CA109446NCI NIH HHS R01 CA181088NIAID NIH HHS AI084913NIAID NIH HHS R01 AI084913NIAID NIH HHS R37 AI084913NIDCR NIH HHS T90 DE022732NIDCR NIH HHS T90DE022732
6 · The paper itself

Abstract

Tumor progression occurs through the modulation of a number of physiological parameters, including the development of immunosuppressive mechanisms to prevent immune detection and response. Among these immune evasion mechanisms, the mobilization of myeloid-derived suppressor cells (MDSC) is a major contributor to the suppression of antitumor T-cell immunity. Patients with renal cell carcinoma (RCC) show increased MDSC, and methods are being explored clinically to reduce the prevalence of MDSC and/or inhibit their function. In the present study, we investigated the relationship between MDSC and the therapeutic potential of a TRAIL-encoding recombinant adenovirus (Ad5-TRAIL) in combination with CpG-containing oligodeoxynucleotides (Ad5-TRAIL/CpG) in an orthotopic mouse model of RCC. This immunotherapy effectively clears renal (Renca) tumors and enhances survival, despite the presence of a high frequency of MDSC in the spleens and primary tumor-bearing kidneys at the time of treatment. Subsequent analyses revealed that the CpG component of the immunotherapy was responsible for decreasing the frequency of MDSC in Renca-bearing mice; further, treatment with CpG modulated the phenotype and function of MDSC that remained after immunotherapy and correlated with an increased T-cell response. Interestingly, the CpG-dependent alterations in MDSC frequency and function did not occur in tumor-bearing mice complicated with diet-induced obesity. Collectively, these data suggest that in addition to its adjuvant properties, CpG also enhances antitumor responses by altering the number and function of MDSC.

Indexed as

AdenoviridaeAnimalsCarcinoma, Renal CellCD8-Positive T-LymphocytesCell Line, TumorCell ProliferationFemaleImmunotherapyKidneyKidney NeoplasmsMiceMice, Inbred BALB CMyeloid CellsObesityOligodeoxyribonucleotidesOligonucleotidesCPG-oligonucleotideOligodeoxyribonucleotidesOligonucleotidesTNF-Related Apoptosis-Inducing Ligand

Identifiers

PMID25143233
PMCPMC4412276
OpenAlexW2037387716

What OpenQuestion holds

Textmetadata
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.