Evidence map›Paper›PMID 22361816›Full record

ArticleCancer gene therapy2012

Targeting dendritic cells with antigen via dendritic cell-associated promoters.

V Moulin, M E Morgan, D Eleveld-Trancikova, J B A G Haanen, E Wielders, M W G Looman, R A J Janssen, C G Figdor, B J H Jansen, G J Adema

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In one paragraph

Article in Cancer gene therapy, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

15 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. DNA Vaccines-How Far From Clinical Use?International journal of molecular sciences · 2018
    Review
  9. DNA vaccines for prostate cancer.Pharmacology & therapeutics · 2017
    Review
  10. MicroRNA-regulated viral vectors for gene therapy.World journal of experimental medicine · 2016
    Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. 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

10 authors at 4 institutions in 1 country.

V MoulinDepartment of Tumor Immunology, Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
M E Morgan
D Eleveld-Trancikova
J B A G Haanen
E Wielders
M W G Looman
R A J Janssen
C G Figdor
B J H Jansen
G J Adema
Radboud Institute for Molecular Life Sciences · NLRadboud University Medical Center · NLRadboud University Nijmegen · NLThe Netherlands Cancer Institute · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The induction of tumor-specific immune responses is largely dependent on the ability of dendritic cells (DCs) to present tumor-associated antigens to T lymphocytes. Therefore, we investigated the use of DC-associated promoter-driven genetic vaccines to specifically target DC in vivo. Restricted expression of vaccine-encoding genes in DC should enhance specificity and improves their safety for clinical applications. Hereto, 3-5 kb upstream sequences of the murine genes encoding CD11c, DC-SIGN, DC-STAMP and Langerin were isolated, characterized and subcloned into enhanced green fluorescent protein (EGFP) reporter constructs. Upon electroporation, EGFP was expressed in DC cell lines, but not in other cell lines, confirming DC-restricted promoter activity. When these promoters were cloned into a construct upstream of the gene for ovalbumin (OVA), it appeared that DC-STAMP promoter-driven expression of OVA (pDCSTAMP/OVA) in DC yielded the most efficient OVA-specific CD4+ and CD8+ T-cell responses in vitro. Administration of pDC-STAMP/OVA in vivo, using the tattoo gun vaccination system, evoked specific immune responses as evidenced in a mouse tumor model. Adoptively transferred pDC-STAMP/OVA-transfected DCs induced strong CD8+ T-cell proliferation in vivo. These experiments demonstrate that our DC-directed promoter constructs are potential tools to restrict antigen expression in DC and could be implemented to modulate DC function by the introduction of relevant proteins.

Indexed as

AnimalsAntigen PresentationAntigens, NeoplasmCD11c AntigenCell Adhesion MoleculesDC-Specific ICAM-3 Grabbing NonintegrinDendritic CellsFemaleImmunotherapy, AdoptiveLectins, C-TypeMelanoma, ExperimentalMembrane ProteinsMiceMice, Inbred C57BLMice, TransgenicNerve Tissue ProteinsAntigens, NeoplasmCD11c AntigenCell Adhesion MoleculesDC-Specific ICAM-3 Grabbing NonintegrinDC-STAMP protein, mouseLectins, C-TypeMembrane ProteinsNerve Tissue ProteinsReceptors, Cell SurfaceVaccines, DNA

Identifiers

PMID22361816
OpenAlexW1973083737

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.