Evidence map›Paper›PMID 28755290›Full record

ReviewVirus genes2017

Barriers to systemic application of virus-based vectors in gene therapy: lessons from adenovirus type 5.

Franziska Jönsson, Florian Kreppel

Abstract readReview
PubMed Publisher
In one paragraph

Review in Virus genes, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Adenovirus-Antibody Complexes Contributed to Lethal Systemic Inflammation in a Gene Therapy Trial.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Article
  11. Article
  12. Article
  13. Article
  14. 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

2 authors.

Franziska JönssonChair of Biochemistry and Molecular Medicine, Center for Biomedical Research and Education (ZBAF), Witten/Herdecke University (UW/H), Stockumer Straße 10, 58453, Witten, Germany.
Florian KreppelChair of Biochemistry and Molecular Medicine, Center for Biomedical Research and Education (ZBAF), Witten/Herdecke University (UW/H), Stockumer Straße 10, 58453, Witten, Germany. florian.kreppel@uni-wh.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Currently, virus-based vectors, namely derivatives of the adenovirus, are frequently used in a wide variety of ex vivo or local gene therapeutic applications. However, the efficacy of virus-based vectors in systemic applications is presently still extremely limited. Complex interactions of the various vector types with the patient's organism hinder successful vector deployment. Exemplary, here we summarize barriers to systemic application of Adenovirus-based vectors leading either to acute toxic effects or rapid vector neutralization and discuss strategies to overcome these barriers aiming to develop more efficient vector types.

Indexed as

AdenoviridaeAnimalsGenetic TherapyGenetic VectorsHumansAdenovirusShieldingVector-host interactionVector neutralizationVirus-based vector

Identifiers

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.