Evidence map›Paper›PMID 39684442›Full record

ArticleInternational journal of molecular sciences2024

In Vivo Selection of S/MAR Sequences to Favour AAV Episomal Maintenance in Dividing Cells.

Andrea Llanos-Ardaiz, Aquilino Lantero, Leire Neri, Itsaso Mauleón, Marina Ruiz de Galarreta, Laia Trigueros-Motos, Nicholas D Weber, Veronica Ferrer, Rafael Aldabe, Gloria Gonzalez-Aseguinolaza

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

10 authors.

Andrea Llanos-ArdaizVivet Therapeutics S.L., 31008 Pamplona, Spain.ORCID 0009-0004-5511-5064
Aquilino LanteroVivet Therapeutics S.L., 31008 Pamplona, Spain.ORCID 0000-0003-3928-9895
Leire NeriVivet Therapeutics S.L., 31008 Pamplona, Spain.
Itsaso MauleónDNA & RNA Medicine Division, Centre for Applied Medical Research (CIMA), University of Navarra, 31009 Pamplona, Spain.
Marina Ruiz de GalarretaVivet Therapeutics S.L., 31008 Pamplona, Spain.ORCID 0000-0001-9666-8416
Laia Trigueros-MotosVivet Therapeutics S.L., 31008 Pamplona, Spain.
Nicholas D WeberVivet Therapeutics S.L., 31008 Pamplona, Spain.ORCID 0000-0002-3584-644X
Veronica FerrerVivet Therapeutics S.A.S., 75008 Paris, France.
Rafael AldabeDNA & RNA Medicine Division, Centre for Applied Medical Research (CIMA), University of Navarra, 31009 Pamplona, Spain.ORCID 0000-0002-9461-020X
Gloria Gonzalez-AseguinolazaVivet Therapeutics S.L., 31008 Pamplona, Spain.ORCID 0000-0002-1600-4562

Funding

Gobierno de Navarra 0011-1365- 2021-000276
6 · The paper itself

Abstract

Adeno-associated viral (AAV) vector-mediated gene therapy has emerged as a promising alternative to liver transplantation for monogenic metabolic hepatic diseases. AAVs are non-integrative vectors that are maintained primarily as episomes in quiescent cells like adult hepatocytes. This quality, while advantageous from a safety perspective due to a decreased risk of insertional mutagenesis, becomes a disadvantage when treating dividing cells, as it inevitably leads to the loss of the therapeutic genome. This is a challenge for the treatment of hereditary liver diseases that manifest in childhood. One potential approach to avoid vector genome loss involves putting scaffold/matrix attachment regions (S/MARs) into the recombinant AAV (rAAV) genome to facilitate its replication together with the cellular genome. We found that the administration of AAVs carrying the human β-interferon S/MAR sequence to neonatal and infant mice resulted in the maintenance of higher levels of viral genomes. However, we also observed that its inclusion at the 3' end of the mRNA negatively impacted its stability, leading to reduced mRNA and protein levels. This effect can be partially attenuated by incorporating nonsense-mediated decay (NMD)-inhibitory sequences into the S/MAR containing rAAV genome, whose introduction may aid in the development of more efficient and longer-lasting gene therapy rAAV vectors.

Indexed as

DependovirusGenetic TherapyGenetic VectorsPlasmidsAnimalsGenome, ViralHumansInterferon-betaMatrix Attachment RegionsMiceVirus ReplicationInterferon-betaAAVepisomal maintenancegene therapyliverNMDreplicationS/MAR

Identifiers

PMID39684442
PMCPMC11641770

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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.