Evidence map›Paper›PMID 35859364›Full record

ArticleHuman gene therapy2022

Improving Lentiviral Transduction of Human Adipose-Derived Mesenchymal Stem Cells.

Kevin Collon, Matthew C Gallo, Jennifer A Bell, Stephanie W Chang, John Croom Sueiro Rodman, Osamu Sugiyama, Donald B Kohn, Jay R Lieberman

Open access · greenAbstract read
In one paragraph

Article in Human gene therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

3 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Identification of a small molecule for enhancing lentiviral transduction of T cells.Molecular therapy. Methods & clinical development · 2023
    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

8 authors at 2 institutions in 1 country.

Kevin CollonDepartment of Orthopaedic Surgery, Keck School of Medicine of the University of Southern California, Los Angeles, California, USA.ORCID 0000-0001-8984-2447
Matthew C GalloDepartment of Orthopaedic Surgery, Keck School of Medicine of the University of Southern California, Los Angeles, California, USA.
Jennifer A BellDepartment of Orthopaedic Surgery, Keck School of Medicine of the University of Southern California, Los Angeles, California, USA.
Stephanie W ChangDepartment of Orthopaedic Surgery, Keck School of Medicine of the University of Southern California, Los Angeles, California, USA.
John Croom Sueiro RodmanSouthern California Clinical and Translational Science Institute, University of Southern California, Los Angeles, California, USA; and.
Osamu SugiyamaDepartment of Orthopaedic Surgery, Keck School of Medicine of the University of Southern California, Los Angeles, California, USA.
Donald B KohnDepartment of Microbiology, Immunology and Molecular Genetics, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California, USA.
Jay R LiebermanDepartment of Orthopaedic Surgery, Keck School of Medicine of the University of Southern California, Los Angeles, California, USA.
University of Southern California · USUniversity of California, Los Angeles · US

Funding

Southern California Clinical and Translational Science InstituteUL1TR001855 · NCATS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Thomas A Buchanan, Michele D. Kipke · 2016 to 2026
$81.3M
The Use of Regional Gene Delivery to Heal Critical Sized Bone DefectsR01AR057076 · NIAMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI LIEBERMAN, JAY R. · 2010 to 2021
$3.9M
NCATS NIH HHS UL1 TR001855NIAMS NIH HHS R01 AR057076
6 · The paper itself

Abstract

Lentiviral transduction of human mesenchymal stem cells (MSCs) induces long-term transgene expression and holds great promise for multiple gene therapy applications. Polybrene is the most commonly used reagent to improve viral gene transfer efficiency in laboratory research; however, it is not approved for human use and has also been shown to impair MSC proliferation and differentiation. Therefore, there is a need for optimized transduction protocols that can also be adapted to clinical settings. LentiBOOST (LB) and protamine sulfate are alternative transduction enhancers (TEs) that can be manufactured to current Good Manufacturing Practice standards, are easily applied to existing protocols, and have been previously studied for the transduction of human CD34

Indexed as

LentivirusMesenchymal Stem CellsCell DifferentiationGenetic VectorsHexadimethrine BromideHumansProtaminesTransduction, GeneticHexadimethrine BromideProtaminesgene therapylentiboostlentivirusmesenchymal stem celltransduction enhancer

Identifiers

PMID35859364
PMCPMC9808795
OpenAlexW4286208740

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.