Evidence map›Paper›PMID 23229093›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2013

Crosstalk between immune cell and oncolytic vaccinia therapy enhances tumor trafficking and antitumor effects.

Padma Sampath, Jun Li, Weizhou Hou, Hannah Chen, David L Bartlett, Steve H Thorne

Open access · bronzeAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

35 citing papers in PubMed, 50 citations in OpenAlex.

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  17. Checkpoint inhibitors go viral.Nature biotechnology · 2019
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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

6 authors at 1 institution in 1 country.

Padma SampathDepartment of Surgery, University of Pittsburgh Cancer Institute, Pittsburgh, PA, USA.
Jun Li
Weizhou Hou
Hannah Chen
David L Bartlett
Steve H Thorne
UPMC Hillman Cancer Center · US

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Jessie Nedrow · 1988 to 2026
$158.0M
Type-1 Antigen Presenting Cells in CNS Tumors - Key to Efficient Anti-Tumor T-CelP01CA132714 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KALINSKI, PAWEL · 2009 to 2013
$6.8M
Enhancing Delivery and Regulating Gene Expression in Oncolytic Vaccinia VectorsR01CA140215 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI THORNE, STEPHEN H · 2010 to 2014
$1.5M
NCI NIH HHS P01 CA132714NCI NIH HHS P30 CA047904NCI NIH HHS P30 CA047904-21S3NCI NIH HHS R01 CA140215
6 · The paper itself

Abstract

The combination of an oncolytic virus, that directly destroys tumor cells and mediates an acute immune response, with an immune cell therapy, capable of further enlisting and enhancing the host immune response, has the potential to create a potent therapeutic effect. We have previously developed several strategies for optimizing the delivery of oncolytic vaccinia virus vectors to their tumor targets, including the use of immune cell-based carrier vehicles and the incorporation of mutations that increase production of the enveloped form of vaccinia (extracellular enveloped viral (EEV)) that is better adapted to spread within a host. Here, we initially combine these approaches to create a novel therapeutic, consisting of an immune cell (cytokine-induced killer, CIK) preloaded with an oncolytic virus that is EEV enhanced. This resulted in direct interaction between the viral and immune cell components with each assisting the other in directing the therapy to the tumor and so enhancing the antitumor effects. This effect could be further improved through CCL5 expression from the virus. The resulting multicomponent therapy displays the ability for synergistic crosstalk between components, so significantly enhancing tumor trafficking and antitumor effects.

Indexed as

AnimalsAntineoplastic AgentsCell Line, TumorChemokine CCL5Cytokine-Induced Killer CellsFemaleGenetic VectorsHumansMiceMice, Inbred BALB CMice, Inbred C57BLNeoplasmsOncolytic VirotherapyOncolytic VirusesVaccinia virusVirus ReplicationAntineoplastic AgentsChemokine CCL5

Identifiers

PMID23229093
PMCPMC3589162
OpenAlexW2001437130

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.