Evidence map›Paper›PMID 10559360›Full record

ArticleJournal of virology1999

Dendritic cells transduced with an adenovirus vector encoding Epstein-Barr virus latent membrane protein 2B: a new modality for vaccination.

E Ranieri, W Herr, A Gambotto, W Olson, D Rowe, P D Robbins, L S Kierstead, S C Watkins, L Gesualdo, W J Storkus

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

12 citing papers in PubMed, 76 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. DC expressing transgene Foxp3 are regulatory APC.European journal of immunology · 2010
    Article
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  6. Article
  7. Article
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  11. Human tumor-derived genomic DNA transduced into a recipient cell induces tumor-specific immune responses ex vivo.Proceedings of the National Academy of Sciences of the United States of America · 2002
    Article
  12. 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 at 2 institutions in 1 country.

E RanieriDepartments of Surgery, Pittsburgh, Pennsylvania 15261, USA.
W Herr
A Gambotto
W Olson
D Rowe
P D Robbins
L S Kierstead
S C Watkins
L Gesualdo
W J Storkus
University of Pittsburgh · USUniversity of Pittsburgh Medical Center · US

Funding

IDENTIFICATION OF CLASS I-PRESENTED MELANOMA PEPTIDESR01CA057840 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI STORKUS, WALTER J · 1993 to 2007
$1.8M
NCI NIH HHS CA 143666NCI NIH HHS CA 57840NCI NIH HHS R01 CA057840
6 · The paper itself

Abstract

Epstein-Barr virus (EBV) is a herpesvirus commonly associated with several malignancies, particularly in immunocompromised hosts. As a strategy for stimulating immunity against EBV for the treatment of EBV-associated tumors, we have genetically engineered dendritic cells (DC) to express EBV antigens, such as latent membrane protein 2B (LMP2B), using recombinant adenovirus vectors. CD8(+) T lymphocytes from HLA-A2.1(+), EBV-seropositive healthy donors were cultured with autologous DC infected with recombinant adenovirus vector AdEGFP, encoding an enhanced green fluorescent protein (EGFP), or AdLMP2B at a multiplicity of infection of 250. After 48 h, >95% of the DC were positive for EGFP expression as assessed by fluorescence-activated cell sorting analysis, indicating efficient gene transfer. AdLMP2-transduced DC were used to stimulate CD8(+) T cells. Responder CD8(+) T cells were tested for gamma interferon (IFN-gamma) release by enzyme-linked spot (ELISPOT) assay and cytotoxic activity. Prior to in vitro stimulation, the frequencies of T-cells directed against two HLA-A2-presented LMP2 peptides (LMP2 329-337 and LMP2 426-434) were very low as assessed by IFN-gamma spot formation (T-cell frequency, <0.003%). IFN-gamma ELISPOT assays performed at day 14 showed a significant (2-log) increase of the day 0 frequency of T cells reactive against the LMP2 329-337 peptide, from 0.003 to 0.3 (P < 0.001). Moreover, specific cytolytic activity was observed against the autologous EBV B-lymphoblastoid cell lines after 21 days of stimulation of T-cell responders with AdLMP2-transduced DC (P < 0.01). In summary, autologous mature DC genetically modified with an adenovirus encoding EBV antigens stimulate the generation of EBV-specific CD8(+) effector T cells in vitro, supporting the potential application of EBV-based adenovirus vector vaccination for the immunotherapy of the EBV-associated malignancies.

Indexed as

Adenoviruses, HumanAntigen PresentationCD8-Positive T-LymphocytesCells, CulturedCell Transformation, ViralDendritic CellsGenetic VectorsGene Transfer TechniquesHerpesvirus 4, HumanHLA-A2 AntigenHumansImmunophenotypingPeptidesTransduction, GeneticVaccines, DNAViral Matrix ProteinsEBV-associated membrane antigen, Epstein-Barr virusHLA-A2 AntigenPeptidesVaccines, DNAViral Matrix ProteinsViral Vaccines

Identifiers

PMID10559360
PMCPMC113097
OpenAlexW1556098051

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.