Evidence map›Paper›PMID 25658613›Full record

ArticleJournal of immunotherapy (Hagerstown, Md. : 1997)

Virological and preclinical characterization of a dendritic cell targeting, integration-deficient lentiviral vector for cancer immunotherapy.

Jared M Odegard, Brenna Kelley-Clarke, Semih U Tareen, David J Campbell, Patrick A Flynn, Christopher J Nicolai, Megan M Slough, Chintan D Vin, Patrick J McGowan, Lisa T Nelson and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of immunotherapy (Hagerstown, Md. : 1997). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

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  12. The feasibility of incorporating Vpx into lentiviral gene therapy vectors.Molecular therapy. Methods & clinical development · 2016
    Article
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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

13 authors at 2 institutions in 1 country.

Jared M Odegard*Immune Design Corp. †TRIA Bioscience Corp., Seattle, WA.
Brenna Kelley-Clarke
Semih U Tareen
David J Campbell
Patrick A Flynn
Christopher J Nicolai
Megan M Slough
Chintan D Vin
Patrick J McGowan
Lisa T Nelson
Jan Ter Meulen
Thomas W Dubensky
Scott H Robbins
Metis Design Corporation (United States) · USTRIA Bioscience (United States) · US

Funding

A novel DC-targeting non-integrating lentivector vaccine for HIV infectionR43AI087444 · NIAID · TRIA BIOSCIENCE CORPORATION · PI ROBBINS, SCOTT H · 2010 to 2011
$600k
NIAID NIH HHS 1R43AI087444-01NIAID NIH HHS R43 AI087444
6 · The paper itself

Abstract

Dendritic cells (DCs) are essential antigen-presenting cells for the initiation of cytotoxic T-cell responses and therefore attractive targets for cancer immunotherapy. We have developed an integration-deficient lentiviral vector termed ID-VP02 that is designed to deliver antigen-encoding nucleic acids selectively to human DCs in vivo. ID-VP02 utilizes a genetically and glycobiologically engineered Sindbis virus glycoprotein to target human DCs through the C-type lectin DC-SIGN (CD209) and also binds to the homologue murine receptor SIGNR1. Specificity of ID-VP02 for antigen-presenting cells in the mouse was confirmed through biodistribution studies showing that following subcutaneous administration, transgene expression was only detectable at the injection site and the draining lymph node. A single immunization with ID-VP02 induced a high level of antigen-specific, polyfunctional effector and memory CD8 T-cell responses that fully protected against vaccinia virus challenge. Upon homologous readministration, ID-VP02 induced a level of high-quality secondary effector and memory cells characterized by stable polyfunctionality and expression of IL-7Rα. Importantly, a single injection of ID-VP02 also induced robust cytotoxic responses against an endogenous rejection antigen of CT26 colon carcinoma cells and conferred both prophylactic and therapeutic antitumor efficacy. ID-VP02 is the first lentiviral vector which combines integration deficiency with DC targeting and is currently being investigated in a phase I trial in cancer patients.

Indexed as

Cancer VaccinesGenetic VectorsImmunotherapy, AdoptiveAnimalsCarcinomaCD8-Positive T-LymphocytesCell Adhesion MoleculesCell Line, TumorClinical Trials, Phase I as TopicColonic NeoplasmsCytotoxicity, ImmunologicDC-Specific ICAM-3 Grabbing NonintegrinDendritic CellsGenetic EngineeringGlycoproteinsHumansCancer VaccinesCell Adhesion MoleculesDC-Specific ICAM-3 Grabbing NonintegrinGlycoproteinsinterleukin-7 receptor, alpha chainLectins, C-TypeReceptors, Cell SurfaceReceptors, Interleukin-7Viral Proteins

Identifiers

PMID25658613
PMCPMC4323576
OpenAlexW2316952126

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.