Evidence map›Paper›PMID 26752352›Full record

ArticleGene therapy2016

Establishment of two quantitative nested qPCR assays targeting the human EPO transgene.

E W I Neuberger, I Perez, C Le Guiner, D Moser, T Ehlert, M Allais, P Moullier, P Simon, R O Snyder

Abstract read
PubMed Publisher
In one paragraph

Article in Gene therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 32 citations in OpenAlex.

  1. [Gene doping: current test methods and analytical challenges].Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz · 2026
    Review
  2. Article
  3. Article
  4. Review
  5. PCR-Based Equine Gene Doping Test for the Australian Horseracing Industry.International journal of molecular sciences · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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

9 authors at 5 institutions in 3 countries.

E W I NeubergerFaculty of Social Science, Media and Sport, Department of Sports Medicine, Johannes Gutenberg-University Mainz, Mainz, Germany.
I PerezDepartment of Molecular Genetics and Microbiology, University of Florida, College of Medicine, Gainesville, FL, USA.
C Le GuinerINSERM UMR1089, Atlantic Gene Therapies, CHU de Nantes, Université de Nantes, Nantes, France.
D MoserFaculty of Social Science, Media and Sport, Department of Sports Medicine, Johannes Gutenberg-University Mainz, Mainz, Germany.
T EhlertFaculty of Social Science, Media and Sport, Department of Sports Medicine, Johannes Gutenberg-University Mainz, Mainz, Germany.
M AllaisINSERM UMR1089, Atlantic Gene Therapies, CHU de Nantes, Université de Nantes, Nantes, France.
P MoullierDepartment of Molecular Genetics and Microbiology, University of Florida, College of Medicine, Gainesville, FL, USA.
P SimonFaculty of Social Science, Media and Sport, Department of Sports Medicine, Johannes Gutenberg-University Mainz, Mainz, Germany.
R O SnyderDepartment of Molecular Genetics and Microbiology, University of Florida, College of Medicine, Gainesville, FL, USA.
Johannes Gutenberg University Mainz · DEUniversity of Florida · USCentre Hospitalier Universitaire de Nantes · FRFlorida College · USGenethon (France) · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

For ethical and safety reasons it is critical to develop easily implemented assays with high sensitivity and specificity for gene doping surveillance. Two nested quantitative real-time PCR (qPCR) assays were developed that target the human EPO (hEPO) cDNA sequence in a circular form, representative of recombinant adeno-associated viral (rAAV) vector genomes found in vivo. Through an interlaboratory evaluation, the assays were validated and utilized in an in vitro blinded study. These assays are specific and extremely sensitive with a limit of detection (LOD) of 1 copy of circular plasmid DNA and a limit of quantification (LOQ) of 10 to 20 copies in the presence of 500 ng of human genomic DNA (hgDNA) extracted from WBCs. Additionally, using the two nested qPCR assays in a non-human primate study, where macaques were injected intramuscularly with a rAAV8 vector harboring a promoterless hEPO cDNA sequence, the viral vector was detected 8 to 14 weeks post-injection in macaque WBCs. The high sensitivity of the nested qPCR approach along with the capability of quantifying target DNA, make this approach a reliable tool for gene doping surveillance and the monitoring of exogenous DNA sequences.

Indexed as

TransgenesAnimalsDNADoping in SportsErythropoietinGenetic VectorsHumansMacacaMacaca fascicularisMalePlasmidsPolymerase Chain ReactionReal-Time Polymerase Chain ReactionSensitivity and SpecificityDNAEPO protein, humanErythropoietin

Identifiers

PMID26752352
OpenAlexW2236091866

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.