Evidence map›Paper›PMID 21228879›Full record

ArticleGene therapy2011

Treatment of canine leukocyte adhesion deficiency by foamy virus vectors expressing CD18 from a PGK promoter.

T R Bauer, E M Olson, Y Huo, L M Tuschong, J M Allen, Y Li, T H Burkholder, D W Russell

Open access · greenAbstract readEvaluation Study
In one paragraph

Article in Gene therapy, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Long-term follow-up of foamy viral vector-mediated gene therapy for canine leukocyte adhesion deficiency.Molecular therapy : the journal of the American Society of Gene Therapy · 2013
    Article
  10. Article
  11. Review
  12. Thymidine kinase suicide gene-mediated ganciclovir ablation of autologous gene-modified rhesus hematopoiesis.Molecular therapy : the journal of the American Society of Gene Therapy · 2012
    Article
  13. The function of dog models in developing gene therapy strategies for human health.Mammalian genome : official journal of the International Mammalian Genome Society · 2011
    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

8 authors at 4 institutions in 1 country.

T R BauerExperimental Transplantation and Immunology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
E M Olson
Y Huo
L M Tuschong
J M Allen
Y Li
T H Burkholder
D W Russell
University of Washington · USNational Cancer Institute · USOffice of Research Services · USSeattle University · US

Funding

VECTOR CONSTRUCTIONS FOR GENE THERAPY OF SICKLE CELL DISEASEP01HL053750 · NHLBI · UNIVERSITY OF WASHINGTON · PI RUSSELL, DAVID W · 1994 to 2014
$30.4M
Treatment of Leukocyte Adhesion Deficiency by Foamy Virus VectorsR01HL085107 · NHLBI · UNIVERSITY OF WASHINGTON · PI RUSSELL, DAVID W · 2006 to 2016
$4.2M
Intramural NIH HHSNHLBI NIH HHS HL085107NHLBI NIH HHS HL53750NHLBI NIH HHS P01 HL053750NHLBI NIH HHS R01 HL085107
6 · The paper itself

Abstract

Proto-oncogene activation caused by retroviral vector integration can cause malignancies in gene therapy trials. This has led investigators to search for less genotoxic vectors with minimal enhancer activity and a decreased risk of influencing neighboring chromosomal gene expression after integration. We previously showed that foamy virus (FV) vectors expressing the canine CD18 gene from an internal murine stem cell virus (MSCV) promoter could cure canine leukocyte adhesion deficiency (LAD). Here, we have repeated these studies using a FV vector expressing canine CD18 from a phosphoglycerate kinase (PGK) gene promoter. In vitro analysis showed that this vector did not contain an enhancer that activated neighboring genes, and it expressed CD18 efficiently in canine neutrophils and CD34+ cells. However, dogs that received hematopoietic stem cells transduced with the PGK-CD18 vector continued to suffer from LAD, and sometimes died prematurely of the disease. These studies show that the PGK promoter cannot effectively replace the MSCV promoter in CD18-expressing FV vectors, and they suggest that vectors containing a strong promoter-enhancer may be necessary for the treatment of human LAD.

Indexed as

Genetic TherapyGenetic VectorsAnimalsCD18 AntigensDogsHematopoietic Stem Cell TransplantationLeukocyte-Adhesion Deficiency SyndromeLeukocytesModels, AnimalNeutrophilsPhosphoglycerate KinasePromoter Regions, GeneticProto-Oncogene MasSpumavirusCD18 AntigensMAS1 protein, humanPhosphoglycerate KinaseProto-Oncogene Mas

Identifiers

PMID21228879
PMCPMC3079787
OpenAlexW1992866551

What OpenQuestion holds

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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.