Evidence map›Paper›PMID 11223992›Full record

ArticleGene therapy2000

Plasmid DNA adsorbed onto cationic microparticles mediates target gene expression and antigen presentation by dendritic cells.

K S Denis-Mize, M Dupuis, M L MacKichan, M Singh, B Doe, D O'Hagan, J B Ulmer, J J Donnelly, D M McDonald, G Ott

Abstract read
PubMed Publisher
In one paragraph

Article in Gene therapy, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
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

25 citing papers in PubMed.

  1. Emerging Cationic Nanovaccines.Pharmaceutics · 2024
    Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Polymeric Materials for Gene Delivery and DNA Vaccination.Advanced materials (Deerfield Beach, Fla.) · 2009
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Enhanced antigen presentation and immunostimulation of dendritic cells using acid-degradable cationic nanoparticles.Journal of controlled release : official journal of the Controlled Release Society · 2005
    Article
  12. Article
  13. Article
  14. Novel approaches to vaccine delivery.Pharmaceutical research · 2004
    Review
  15. PLGA-PEI nanoparticles for gene delivery to pulmonary epithelium.European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V · 2004
    Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article
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.

K S Denis-MizeDepartment of Anatomy, and Cardiovascular Research Institute, University of California San Francisco, San Francisco, CA, USA.
M Dupuis
M L MacKichan
M Singh
B Doe
D O'Hagan
J B Ulmer
J J Donnelly
D M McDonald
G Ott

Funding

Tools for Analysis of Airway InflammationP01HL024136 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KRUMMEL, MATTHEW F · 1985 to 2014
$23.3M
NHLBI NIH HHS HL24136
6 · The paper itself

Abstract

Dendritic cells (DC) play a key role in antigen presentation and activation of specific immunity. Much current research focuses on harnessing the potency of DC for vaccines, gene therapy, and cancer immunotherapy applications. However, DC are not readily transfected in vitro by traditional nonviral techniques. A novel DNA vaccine formulation was used to determine if DC are transfected in vitro. The formulation consists of plasmid DNA adsorbed on to cationic microparticles composed of the biodegradable polymer polylactide-co-glycolide (PLG) and the cationic surfactant, cetyltrimethylammonium bromide (CTAB). Using preparations of fluorescent-labeled plasmid DNA formulated on PLG-CTAB microparticles to study internalization by macrophages and dendritic cells in vitro and in vivo, we found that most, but not all, of the fluorescence was concentrated in endosomal compartments. Furthermore, uptake of plasmid DNA encoding HIV p55 gag adsorbed to PLG-CTAB microparticles by murine bone marrow-derived dendritic cells resulted in target gene expression, as detected by RT-PCR. The antigen was subsequently processed and presented, resulting in stimulation of an H-2kd-restricted, gag-specific T cell hybridoma. Activation of the hybridoma, detected by IL-2 production, was dose-dependent in the range of 0.1-20 microg DNA (10-2000 microg PLG) and was sustained up to 5 days after transfection. Thus, adsorption of plasmid DNA on PLG-CTAB microparticles provides a potentially useful nonviral approach for in vitro transfection of dendritic cells. Gene Therapy (2000) 7, 2105-2112.

Indexed as

Antigen PresentationGene Products, gagAdsorptionAnalysis of VarianceAnimalsCetrimoniumCetrimonium CompoundsDendritic CellsFemaleGene ExpressionGenetic TherapyHybridomasImage Processing, Computer-AssistedInterleukin-2Lactic AcidLymphocyte ActivationCetrimoniumCetrimonium CompoundsGene Products, gagInterleukin-2Lactic AcidPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerPolymersVaccines, DNA

Identifiers

PMID11223992

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.