Evidence map›Paper›PMID 27605069›Full record

ReviewImmunotherapy2016

Combination strategies to enhance the potency of monocyte-derived dendritic cell-based cancer vaccines.

Ronald J Fecek, Walter J Storkus

Abstract readReview
In one paragraph

Review in Immunotherapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Immunotherapy and delivery systems for melanoma.Human vaccines & immunotherapeutics · 2024
    Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. 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

2 authors at 1 institution in 1 country.

Ronald J FecekDepartment of Dermatology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
Walter J StorkusDepartment of Dermatology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
University of Pittsburgh · US

Funding

Therapuetic Immune Targeting of EphA2 Expressed by Melanoma & Its Tumor-AssociateP50CA121973 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KIRKWOOD, JOHN MUNN · 2008 to 2018
$22.9M
Combinational Immunotherapy Targeting the Melanoma-Associated VasculatureR01CA169118 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI STORKUS, WALTER J. · 2012 to 2016
$2.1M
Induction of Therapeutic Immunity in the Tumor MicroenvironmentR01CA204419 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI STORKUS, WALTER J. · 2016 to 2020
$1.7M
Vaccines to promote Tc-1-based targeting of tumor stromaR01CA140375 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI STORKUS, WALTER J. · 2010 to 2014
$1.5M
NCI NIH HHS P50 CA121973NCI NIH HHS R01 CA140375NCI NIH HHS R01 CA169118NCI NIH HHS R01 CA204419
6 · The paper itself

Abstract

Dendritic cells (DCs) are potent inducers of adaptive immunity and their clinical use in cancer vaccine formulations remains an area of active translational and clinical investigation. Although cancer vaccines applied as monotherapies have had a modest history of clinical success, there is great enthusiasm for novel therapeutic strategies combining DC-based cancer vaccines with agents that 'normalize' immune function in the tumor microenvironment (TME). Broadly, these combination vaccines are designed to antagonize/remove immunosuppressive networks within the TME that serve to limit the antitumor action of vaccine-induced T cells and/or to condition the TME to facilitate the recruitment and optimal function and durability of vaccine-induced T cells. Such combination regimens are expected to dramatically enhance the clinical potency of DC-based cancer vaccine platforms.

Indexed as

AnimalsAntibodies, MonoclonalCancer VaccinesCombined Modality TherapyCostimulatory and Inhibitory T-Cell ReceptorsDendritic CellsGlucocorticoid-Induced TNFR-Related ProteinHumansImmunotherapyLymphocyte ActivationMonocytesNeoplasmsT-LymphocytesTumor MicroenvironmentAntibodies, MonoclonalCancer VaccinesCostimulatory and Inhibitory T-Cell ReceptorsGlucocorticoid-Induced TNFR-Related ProteinTNFRSF18 protein, humancancercombination immunotherapydendritic cellimmunoconditioningimmunoregulationtargeted therapyvaccine

Identifiers

PMID27605069
PMCPMC5619021
OpenAlexW2511623974

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.