Evidence map›Paper›PMID 23056548›Full record

ArticlePloS one2012

Dendritic cell based PSMA immunotherapy for prostate cancer using a CD40-targeted adenovirus vector.

Briana Jill Williams, Shilpa Bhatia, Lisa K Adams, Susan Boling, Jennifer L Carroll, Xiao-Lin Li, Donna L Rogers, Nikolay Korokhov, Imre Kovesdi, Alexander V Pereboev and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

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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

12 authors at 4 institutions in 1 country.

Briana Jill WilliamsGene Therapy Program, Department of Urology, LSU Health Sciences Center, Shreveport, Louisiana, United States of America.
Shilpa Bhatia
Lisa K Adams
Susan Boling
Jennifer L Carroll
Xiao-Lin Li
Donna L Rogers
Nikolay Korokhov
Imre Kovesdi
Alexander V Pereboev
David T Curiel
J Michael Mathis
Louisiana State University Health Sciences Center Shreveport · USVector (United States) · USUniversity of Alabama at Birmingham · USWashington University in St. Louis · US

Funding

Capsid-incorporation of HIV antigens as a novel adenovirus HIV vaccine approachR33AI076096 · NIAID · WASHINGTON UNIVERSITY · PI CURIEL, DAVID TERRY · 2009 to 2011
$1.5M
Cancer dual-targeting of an infectivity-enhance CRAdR42CA114921 · NCI · VECTORLOGICS, INC. · PI MATHIS, J. MICHAEL · 2008 to 2009
$865k
NCI NIH HHS 2R42-CA114921NCI NIH HHS R42 CA114921NIAID NIH HHS 5R33-AI076096NIAID NIH HHS R33 AI076096
6 · The paper itself

Abstract

Human prostate tumor vaccine and gene therapy trials using ex vivo methods to prime dendritic cells (DCs) with prostate specific membrane antigen (PSMA) have been somewhat successful, but to date the lengthy ex vivo manipulation of DCs has limited the widespread clinical utility of this approach. Our goal was to improve upon cancer vaccination with tumor antigens by delivering PSMA via a CD40-targeted adenovirus vector directly to DCs as an efficient means for activation and antigen presentation to T-cells. To test this approach, we developed a mouse model of prostate cancer by generating clonal derivatives of the mouse RM-1 prostate cancer cell line expressing human PSMA (RM-1-PSMA cells). To maximize antigen presentation in target cells, both MHC class I and TAP protein expression was induced in RM-1 cells by transduction with an Ad vector expressing interferon-gamma (Ad5-IFNγ). Administering DCs infected ex vivo with CD40-targeted Ad5-huPSMA, as well as direct intraperitoneal injection of the vector, resulted in high levels of tumor-specific CTL responses against RM-1-PSMA cells pretreated with Ad5-IFNγ as target cells. CD40 targeting significantly improved the therapeutic antitumor efficacy of Ad5-huPSMA encoding PSMA when combined with Ad5-IFNγ in the RM-1-PSMA model. These results suggest that a CD-targeted adenovirus delivering PSMA may be effective clinically for prostate cancer immunotherapy.

Indexed as

AdenoviridaeAdjuvants, ImmunologicAnimalsAntigen PresentationAntigens, SurfaceATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily B, Member 2ATP Binding Cassette Transporter, Subfamily B, Member 3Cancer VaccinesCD40 AntigensCell Line, TumorCell SurvivalDendritic CellsGenetic VectorsGlutamate Carboxypeptidase IIHLA-A AntigensAdjuvants, ImmunologicAntigens, SurfaceATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily B, Member 2ATP Binding Cassette Transporter, Subfamily B, Member 3Cancer VaccinesCD40 AntigensFOLH1 protein, humanGlutamate Carboxypeptidase IIHLA-A AntigensInterferon-gammaTap1 protein, mouseTap2 protein, mouse

Identifiers

PMID23056548
PMCPMC3466199
OpenAlexW2119454135

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.