Evidence map›Paper›PMID 28345582›Full record

ArticleNature communications2017

Enhancing titres of therapeutic viral vectors using the transgene repression in vector production (TRiP) system.

H E Maunder, J Wright, B R Kolli, C R Vieira, T T Mkandawire, S Tatoris, V Kennedy, S Iqball, G Devarajan, S Ellis and 4 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

23 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. FromImmune network · 2026
    Review
  6. Efficient in vivo generation of CAR T cells using a retargeted fourth-generation lentiviral vector.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  7. Review
  8. Review
  9. Enhancing titers of therapeutic lentiviral vectors using PKC agonists.Molecular therapy. Methods & clinical development · 2025
    Article
  10. Article
  11. Introducing a hemoglobin G-Makassar variant in HSCs by in vivo base editing treats sickle cell disease in mice.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Lentiviral delivered aflibercept OXB-203 for treatment of neovascular AMD.Molecular therapy. Methods & clinical development · 2023
    Article
  16. Review
  17. Article
  18. Review
  19. Rapid Lentiviral Vector Producer Cell Line Generation Using a Single DNA Construct.Molecular therapy. Methods & clinical development · 2020
    Article
  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

14 authors at 1 institution in 1 country.

H E MaunderResearch Department, Oxford BioMedica Ltd., Windrush Court, Transport Way, Oxford OX4 6LT, UK.
J WrightResearch Department, Oxford BioMedica Ltd., Windrush Court, Transport Way, Oxford OX4 6LT, UK.
B R KolliResearch Department, Oxford BioMedica Ltd., Windrush Court, Transport Way, Oxford OX4 6LT, UK.
C R VieiraResearch Department, Oxford BioMedica Ltd., Windrush Court, Transport Way, Oxford OX4 6LT, UK.
T T MkandawireResearch Department, Oxford BioMedica Ltd., Windrush Court, Transport Way, Oxford OX4 6LT, UK.
S TatorisResearch Department, Oxford BioMedica Ltd., Windrush Court, Transport Way, Oxford OX4 6LT, UK.
V KennedyResearch Department, Oxford BioMedica Ltd., Windrush Court, Transport Way, Oxford OX4 6LT, UK.
S IqballResearch Department, Oxford BioMedica Ltd., Windrush Court, Transport Way, Oxford OX4 6LT, UK.
G DevarajanResearch Department, Oxford BioMedica Ltd., Windrush Court, Transport Way, Oxford OX4 6LT, UK.
S EllisResearch Department, Oxford BioMedica Ltd., Windrush Court, Transport Way, Oxford OX4 6LT, UK.
Y LadResearch Department, Oxford BioMedica Ltd., Windrush Court, Transport Way, Oxford OX4 6LT, UK.
N G ClarksonResearch Department, Oxford BioMedica Ltd., Windrush Court, Transport Way, Oxford OX4 6LT, UK.
K A MitrophanousResearch Department, Oxford BioMedica Ltd., Windrush Court, Transport Way, Oxford OX4 6LT, UK.
D C FarleyResearch Department, Oxford BioMedica Ltd., Windrush Court, Transport Way, Oxford OX4 6LT, UK.
Oxford BioMedica (United Kingdom) · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A key challenge in the field of therapeutic viral vector/vaccine manufacturing is maximizing production. For most vector platforms, the 'benchmark' vector titres are achieved with inert reporter genes. However, expression of therapeutic transgenes can often adversely affect vector titres due to biological effects on cell metabolism and/or on the vector virion itself. Here, we exemplify the novel 'Transgene Repression In vector Production' (TRiP) system for the production of both RNA- and DNA-based viral vectors. The TRiP system utilizes a translational block of one or more transgenes by employing the bacterial tryptophan RNA-binding attenuation protein (TRAP), which binds its target RNA sequence close to the transgene initiation codon. We report enhancement of titres of lentiviral vectors expressing Cyclo-oxygenase-2 by 600-fold, and adenoviral vectors expressing the pro-apoptotic gene Bax by >150,000-fold. The TRiP system is transgene-independent and will be a particularly useful platform in the clinical development of viral vectors expressing problematic transgenes.

Indexed as

Genetic VectorsAdenoviridaeBacillus subtilisCodonCyclooxygenase 2Green Fluorescent ProteinsHEK293 CellsHumansProtein BiosynthesisRNATransgenesCodonCyclooxygenase 2Green Fluorescent ProteinsRNA

Identifiers

PMID28345582
PMCPMC5378976
OpenAlexW2600756347

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.