Evidence map›Paper›PMID 28674082›Full record

ArticleCancer immunology research2017

Intratumoral STING Activation with T-cell Checkpoint Modulation Generates Systemic Antitumor Immunity.

Casey R Ager, Matthew J Reilley, Courtney Nicholas, Todd Bartkowiak, Ashvin R Jaiswal, Michael A Curran

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 120 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
120citing papers in PubMed, 2 pooled it
6.9field-weighted citation impact, top 2% 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

120 citing papers in PubMed, 2 syntheses or guidelines pooled it, 174 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
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  18. Cold and hot tumors: from molecular mechanisms to targeted therapy.Signal transduction and targeted therapy · 2024
    Review
  19. Article
  20. Article

60 more citing papers are in PubMed but not listed here.

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

6 authors at 1 institution in 1 country.

Casey R AgerImmunology Program, University of Texas Graduate School of Biomedical Sciences at Houston, Houston, Texas.
Matthew J ReilleyDivision of Cancer Medicine, University of Texas MD Anderson Cancer Center, Houston, Texas.
Courtney NicholasDepartment of Immunology, University of Texas MD Anderson Cancer Center, Houston, Texas.
Todd BartkowiakImmunology Program, University of Texas Graduate School of Biomedical Sciences at Houston, Houston, Texas.
Ashvin R JaiswalImmunology Program, University of Texas Graduate School of Biomedical Sciences at Houston, Houston, Texas.
Michael A CurranImmunology Program, University of Texas Graduate School of Biomedical Sciences at Houston, Houston, Texas. mcurran@mdanderson.org.
The University of Texas MD Anderson Cancer Center · US

Funding

Center for Clinical and Translational Sciences (CCTS)UL1TR000371 · NCATS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MCPHERSON, DAVID D · 2012 to 2016
$13.4M
Center for Clinical and Translational Sciences (CCTS)TL1TR000369 · NCATS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MCPHERSON, DAVID D · 2012 to 2016
$1.9M
NCATS NIH HHS TL1 TR000369NCATS NIH HHS UL1 TR000371
6 · The paper itself

Abstract

Coordinated manipulation of independent immune regulatory pathways in the tumor microenvironment-including blockade of T-cell checkpoint receptors and reversal of suppressive myeloid programs-can render aggressive cancers susceptible to immune rejection. Elevated toxicity associated with combination immunotherapy, however, prevents translation of the most efficacious regimens. We evaluated T-cell checkpoint-modulating antibodies targeting CTLA-4, PD-1, and 4-1BB together with myeloid agonists targeting either STING or Flt3 in the TRAMP-C2 model of prostate cancer to determine whether low-dose intratumoral delivery of these agents could elicit systemic control of multifocal disease. Intratumoral administration of the STING agonist cyclic di-GMP (CDG) or Flt3 Ligand (Flt3L) augmented the therapeutic effect of systemic triple checkpoint modulation and promoted the cure of 75% of mice with bilateral TRAMP-C2; however, when all agents were administered locally, only CDG mobilized abscopal immunity. Combination efficacy correlated with globally enhanced ratios of CD8

Indexed as

AnimalsCD8-Positive T-LymphocytesCell Line, TumorCTLA-4 AntigenCyclic GMPDendritic CellsHumansImmunotherapyLymphocytes, Tumor-InfiltratingMembrane ProteinsMiceNeoplasmsProgrammed Cell Death 1 ReceptorSTING ProteinT-LymphocytesTumor MicroenvironmentCTLA-4 AntigenCTLA4 protein, humanCyclic GMPflt3 ligand proteinMembrane ProteinsPDCD1 protein, humanProgrammed Cell Death 1 ReceptorSting1 protein, mouseSTING ProteinTNFRSF9 protein, humanTumor Necrosis Factor Receptor Superfamily, Member 9

Identifiers

PMID28674082
PMCPMC5547907
OpenAlexW2733430447

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.