Evidence map›Paper›PMID 28726495›Full record

ReviewHuman gene therapy. Clinical development2017

Use of Adeno-Associated Virus Vector for Cardiac Gene Delivery in Large-Animal Surgical Models of Heart Failure.

Michael G Katz, Anthony S Fargnoli, Thomas Weber, Roger J Hajjar, Charles R Bridges

Abstract readReview
In one paragraph

Review in Human gene therapy. Clinical development, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Living myocardial slices for the study of nucleic acid-based therapies.Frontiers in bioengineering and biotechnology · 2023
    Article
  11. AAV capsid engineering identified two novel variants with improved in vivo tropism for cardiomyocytes.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Genetic Delivery and Gene Therapy in Pulmonary Hypertension.International journal of molecular sciences · 2021
    Review
  18. Article
  19. Review
  20. Adipose Tissue: An Emerging Target for Adeno-associated Viral Vectors.Molecular therapy. Methods & clinical development · 2020
    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

5 authors.

Michael G KatzCardiovascular Research Center , Icahn School of Medicine at Mount Sinai, New York, New York.
Anthony S FargnoliCardiovascular Research Center , Icahn School of Medicine at Mount Sinai, New York, New York.
Thomas WeberCardiovascular Research Center , Icahn School of Medicine at Mount Sinai, New York, New York.
Roger J HajjarCardiovascular Research Center , Icahn School of Medicine at Mount Sinai, New York, New York.
Charles R BridgesCardiovascular Research Center , Icahn School of Medicine at Mount Sinai, New York, New York.

Funding

Translational Studies in Heart Failure Gene TherapyR01HL083078 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI BRIDGES, CHARLES R · 2007 to 2018
$9.2M
Anti-AAV Antibodies as an Obstacle to Cardiac AAV Gene TherapyR01HL131404 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI WEBER, THOMAS · 2016 to 2019
$3.3M
NHLBI NIH HHS R01 HL083078NHLBI NIH HHS R01 HL131404
6 · The paper itself

Abstract

The advancement of gene therapy-based approaches to treat heart disease represents a need for clinically relevant animal models with characteristics equivalent to human pathologies. Rodent models of cardiac disease do not precisely reproduce heart failure phenotype and molecular defects. This has motivated researchers to use large animals whose heart size and physiological processes more similar and comparable to those of humans. Today, adeno-associated viruses (AAV)-based vectors are undoubtedly among the most promising DNA delivery vehicles. Here, AAV biology and technology are reviewed and discussed in the context of their use and efficacy for cardiac gene delivery in large-animal models of heart failure, using different surgical approaches. The remaining challenges and opportunities for the use of AAV-based vector delivery for gene therapy applications in the clinic are also highlighted.

Indexed as

AnimalsDependovirusDisease Models, AnimalGenetic TherapyGenetic VectorsGene Transfer TechniquesHeart FailureSpecies SpecificityAAV virusanimal models of heart failurecardiac gene deliveryheart disease

Identifiers

PMID28726495
PMCPMC5655838

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.