Evidence map›Paper›PMID 30191160›Full record

ArticleMolecular therapy. Methods & clinical development2018

A Nontoxic Transduction Enhancer Enables Highly Efficient Lentiviral Transduction of Primary Murine T Cells and Hematopoietic Stem Cells.

Marianne Delville, Tayebeh Soheili, Florence Bellier, Amandine Durand, Adeline Denis, Chantal Lagresle-Peyrou, Marina Cavazzana, Isabelle Andre-Schmutz, Emmanuelle Six

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy. Methods & clinical development, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

30 citing papers in PubMed, 41 citations in OpenAlex.

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  4. Syngeneic CAR T cells engineered for persistent delivery of desired proteins.Journal of controlled release : official journal of the Controlled Release Society · 2025
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  10. Review
  11. Gene Therapy and Gene Editing for β-Thalassemia.Hematology/oncology clinics of North America · 2023
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Combination of lentiviral and genome editing technologies for the treatment of sickle cell disease.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Article
  18. Efficient lentiviral transduction method to gene modify cord blood CD8Molecular therapy. Methods & clinical development · 2021
    Article
  19. Article
  20. 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

9 authors at 6 institutions in 1 country.

Marianne DelvilleLaboratory of Human Lymphohematopoiesis, INSERM UMR 1163, Imagine Institute, Paris, France.
Tayebeh SoheiliLaboratory of Human Lymphohematopoiesis, INSERM UMR 1163, Imagine Institute, Paris, France.
Florence BellierLaboratory of Human Lymphohematopoiesis, INSERM UMR 1163, Imagine Institute, Paris, France.
Amandine DurandLaboratory of Human Lymphohematopoiesis, INSERM UMR 1163, Imagine Institute, Paris, France.
Adeline DenisLaboratory of Human Lymphohematopoiesis, INSERM UMR 1163, Imagine Institute, Paris, France.
Chantal Lagresle-PeyrouLaboratory of Human Lymphohematopoiesis, INSERM UMR 1163, Imagine Institute, Paris, France.
Marina CavazzanaLaboratory of Human Lymphohematopoiesis, INSERM UMR 1163, Imagine Institute, Paris, France.
Isabelle Andre-SchmutzLaboratory of Human Lymphohematopoiesis, INSERM UMR 1163, Imagine Institute, Paris, France.
Emmanuelle SixLaboratory of Human Lymphohematopoiesis, INSERM UMR 1163, Imagine Institute, Paris, France.
Sorbonne Paris Cité · FRDélégation Paris 5 · FRAssistance Publique – Hôpitaux de Paris · FRCentre d'Investigation Clinique Biothérapies NeckerHôpital Necker-Enfants Malades · FRUniversité Paris Cité · FR

Funding

European Research Council 269037
6 · The paper itself

Abstract

Lentiviral vectors have emerged as an efficient, safe therapeutic tool for gene therapy based on hematopoietic stem cells (HSCs) or T cells. However, the monitoring of transduced cells in preclinical models remains challenging because of the inefficient transduction of murine primary T cells with lentiviral vectors, in contrast to gammaretroviral vectors. The use of this later in preclinical proof of concept is not considered as relevant when a lentiviral vector will be used in a clinical trial. Hence, there is an urgent need to develop an efficient transduction protocol for murine cells with lentiviral vectors. Here, we describe an optimized protocol in which a nontoxic transduction enhancer (Lentiboost) enables the efficient transduction of primary murine T cells with lentiviral vectors. The optimized protocol combines low toxicity and high transduction efficiency. We achieved a high-level transduction of murine CD4

Indexed as

gene therapyLentiboostlentiviral transductionmurine CD4+ T cellsmurine CD8+ T cellsmurine Sca1+ cells

Identifiers

PMID30191160
PMCPMC6125771
OpenAlexW2887327262

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.