Evidence map›Paper›PMID 38715734›Full record

ArticleMolecular therapy. Methods & clinical development2024

Epigenetic control of multiple genes with a lentiviral vector encoding transcriptional repressors fused to compact zinc finger arrays.

Davide Monteferrario, Marion David, Satish K Tadi, Yuanyue Zhou, Irène Marchetti, Caroline Jeanneau, Gaëlle Saviane, Coralie F Dupont, Angélique E Martelli, Lynn N Truong and 8 more

Abstract read
In one paragraph

Article in Molecular therapy. Methods & clinical development, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Epigenetic editing: from concept to clinic.Nature reviews. Drug discovery · 2026
    Review
  2. 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

18 authors.

Davide MonteferrarioSangamo Therapeutics France, Allée de la Nertière, F-06560 Valbonne, Sophia-Antipolis, France.
Marion DavidSangamo Therapeutics France, Allée de la Nertière, F-06560 Valbonne, Sophia-Antipolis, France.
Satish K TadiSangamo Therapeutics France, Allée de la Nertière, F-06560 Valbonne, Sophia-Antipolis, France.
Yuanyue ZhouSangamo Therapeutics, 501 Canal Boulevard, Richmond, CA 94804, USA.
Irène MarchettiSangamo Therapeutics France, Allée de la Nertière, F-06560 Valbonne, Sophia-Antipolis, France.
Caroline JeanneauSangamo Therapeutics France, Allée de la Nertière, F-06560 Valbonne, Sophia-Antipolis, France.
Gaëlle SavianeSangamo Therapeutics France, Allée de la Nertière, F-06560 Valbonne, Sophia-Antipolis, France.
Coralie F DupontSangamo Therapeutics France, Allée de la Nertière, F-06560 Valbonne, Sophia-Antipolis, France.
Angélique E MartelliSangamo Therapeutics France, Allée de la Nertière, F-06560 Valbonne, Sophia-Antipolis, France.
Lynn N TruongSangamo Therapeutics, 501 Canal Boulevard, Richmond, CA 94804, USA.
Jason A EshlemanSangamo Therapeutics, 501 Canal Boulevard, Richmond, CA 94804, USA.
Colman C NgSangamo Therapeutics, 501 Canal Boulevard, Richmond, CA 94804, USA.
Marshall W HustonSangamo Therapeutics, 501 Canal Boulevard, Richmond, CA 94804, USA.
Gregory D DavisSangamo Therapeutics, 501 Canal Boulevard, Richmond, CA 94804, USA.
Jason D FontenotSangamo Therapeutics, 501 Canal Boulevard, Richmond, CA 94804, USA.
Andreas ReikSangamo Therapeutics, 501 Canal Boulevard, Richmond, CA 94804, USA.
Maurus de la RosaSangamo Therapeutics France, Allée de la Nertière, F-06560 Valbonne, Sophia-Antipolis, France.
David FenardSangamo Therapeutics France, Allée de la Nertière, F-06560 Valbonne, Sophia-Antipolis, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gene silencing without gene editing holds great potential for the development of safe therapeutic applications. Here, we describe a novel strategy to concomitantly repress multiple genes using zinc finger proteins fused to Krüppel-Associated Box repression domains (ZF-Rs). This was achieved via the optimization of a lentiviral system tailored for the delivery of ZF-Rs in hematopoietic cells. We showed that an optimal design of the lentiviral backbone is crucial to multiplex up to three ZF-Rs or two ZF-Rs and a chimeric antigen receptor. ZF-R expression had no impact on the integrity and functionality of transduced cells. Furthermore, gene repression in ZF-R-expressing T cells was highly efficient

Indexed as

epigeneticKRABlentiviral vectorRepressorZinc finger protein

Identifiers

PMID38715734
PMCPMC11074977

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.