Evidence map›Paper›PMID 40832628›Full record

ArticleMolecular therapy. Nucleic acids2025

A short peptide for efficient cellular mRNA delivery: A potential application for inducing an immune response.

Clémentine Ayélé Teko-Agbo, Emilie Josse, Karidia Konate, Sébastien Deshayes, Pascal de Santa Barbara, Sandrine Faure, Prisca Boisguérin, Eric Vivès

Abstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2025. 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. Article
  2. Self-Assembling Short Peptide Carriers for Gene Delivery.International journal of molecular sciences · 2026
    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.

Clémentine Ayélé Teko-AgboPhyMedExp, University of Montpellier, INSERM, CNRS, Montpellier, France.
Emilie JossePhyMedExp, University of Montpellier, INSERM, CNRS, Montpellier, France.
Karidia KonatePhyMedExp, University of Montpellier, INSERM, CNRS, Montpellier, France.
Sébastien DeshayesPhyMedExp, University of Montpellier, INSERM, CNRS, Montpellier, France.
Pascal de Santa BarbaraPhyMedExp, University of Montpellier, INSERM, CNRS, Montpellier, France.
Sandrine FaurePhyMedExp, University of Montpellier, INSERM, CNRS, Montpellier, France.
Prisca BoisguérinPhyMedExp, University of Montpellier, INSERM, CNRS, Montpellier, France.
Eric VivèsPhyMedExp, University of Montpellier, INSERM, CNRS, Montpellier, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nucleic acid molecules are emerging as potential therapeutic tools, as evidenced by the transfection of small interfering RNA (siRNA) molecules in therapeutic applications and messenger RNAs in immunotherapeutic vaccination. In most cases, these nucleic acids are conditioned as lipid nanoparticles made with different lipid moieties to promote their intracellular delivery. Over the past few years, we have documented the delivery of siRNAs using a single short (15 amino acids) peptide called WRAP5, which follows an extremely simplified formulation phase that enables the formation of nanoparticles with a diameter of 60-80 nm. We indeed demonstrated the expected dose-response reduction in the levels of the targeted proteins. To apply this technology to the cellular delivery of mRNAs, we investigated the ability of the WRAP5 peptide to transfect mRNAs of different sizes and promote the expression of their proteins. These peptide-based nanoparticles, which also have diameters ranging from 60 to 80 nm, showed remarkable stability over time when simply stored at 4°C and fully retained their transfection properties

Indexed as

cell-penetrating peptidesmRNA deliveryMT: Delivery Strategiesnanoparticlevaccine

Identifiers

PMID40832628
PMCPMC12359147

What OpenQuestion holds

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Registered trials

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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.