Evidence map›Paper›PMID 29364266›Full record

ArticleJournal of visualized experiments : JoVE2018

Dextran Enhances the Lentiviral Transduction Efficiency of Murine and Human Primary NK Cells.

Arash Nanbakhsh, Brad Best, Matthew Riese, Sridhar Rao, Li Wang, Jeffrey Medin, Monica S Thakar, Subramaniam Malarkannan

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

12 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Innate immune cells in chimeric antigen receptor therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
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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 3 institutions in 1 country.

Arash NanbakhshLaboratory of Molecular Immunology and Immunotherapy, Blood Research Institute, The Blood Center of Wisconsin.
Brad BestVector Core Lab, Blood Research Institute, The Blood Center of Wisconsin.
Matthew RieseLaboratory of Lymphocyte Biology, Blood Research Institute, The Blood Center of Wisconsin.
Sridhar RaoLaboratory of Stem Cell Transcriptional Regulation, Blood Research Institute, The Blood Center of Wisconsin.
Li WangDepartment of Microbiology and Immunology, The Medical College of Wisconsin.
Jeffrey MedinDepartment of Pediatrics, The Medical College of Wisconsin.
Monica S ThakarDepartment of Pediatrics, The Medical College of Wisconsin.
Subramaniam MalarkannanLaboratory of Molecular Immunology and Immunotherapy, Blood Research Institute, The Blood Center of Wisconsin; Department of Microbiology and Immunology, The Medical College of Wisconsin; Department of Pediatrics, The Medical College of Wisconsin; Department of Medicine, The Medical College of Wisconsin; subra.malar@bcw.edu.
Versiti Blood Center of Wisconsin · USMedical College of Wisconsin · USCollege Station Medical Center · US

Funding

VISTA, a novel checkpoint that suppresses anti-tumor T cell responsesR01CA164225 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI WANG, LI LILY · 2012 to 2023
$3.3M
Molecular signature of inflammationR01CA179363 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI MALARKANNAN, SUBRAMANIAM · 2014 to 2018
$1.6M
Molecular mechanisms of signaling co-ordination in innate lymphocytesR01AI102893 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI MALARKANNAN, SUBRAMANIAM · 2013 to 2016
$1.5M
Effects of diacylglycerol kinase zeta deficiency on CD8+ T cell functionK08CA151893 · NCI · UNIVERSITY OF PENNSYLVANIA · PI RIESE, MATTHEW J · 2010 to 2014
$861k
NCI NIH HHS K08 CA151893NCI NIH HHS R01 CA164225NCI NIH HHS R01 CA179363NIAID NIH HHS R01 AI102893
6 · The paper itself

Abstract

The efficient transduction of specific genes into natural killer (NK) cells has been a major challenge. Successful transductions are critical to defining the role of the gene of interest in the development, differentiation, and function of NK cells. Recent advances related to chimeric antigen receptors (CARs) in cancer immunotherapy accentuate the need for an efficient method to deliver exogenous genes to effector lymphocytes. The efficiencies of lentiviral-mediated gene transductions into primary human or mouse NK cells remain significantly low, which is a major limiting factor. Recent advances using cationic polymers, such as polybrene, show an improved gene transduction efficiency in T cells. However, these products failed to improve the transduction efficiencies of NK cells. This work shows that dextran, a branched glucan polysaccharide, significantly improves the transduction efficiency of human and mouse primary NK cells. This highly reproducible transduction methodology provides a competent tool for transducing human primary NK cells, which can vastly improve clinical gene delivery applications and thus NK cell-based cancer immunotherapy.

Indexed as

AnimalsDextransGenetic TherapyHumansKiller Cells, NaturalLentivirusMiceDextrans

Identifiers

PMID29364266
PMCPMC5908645
OpenAlexW2782567278

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.