Evidence map›Paper›PMID 34842345›Full record

ReviewWiley interdisciplinary reviews. RNA2022

Antisense oligonucleotide: A promising therapeutic option to beat COVID-19.

Anaïs M Quemener, Marie-Dominique Galibert

Abstract readReview
In one paragraph

Review in Wiley interdisciplinary reviews. RNA, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Nicking Activity of M13 Bacteriophage Protein 2.International journal of molecular sciences · 2025
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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

2 authors.

Anaïs M QuemenerUniv Rennes, CNRS, IGDR (Institute of Genetics and Development of Rennes) - UMR 6290, Rennes, France.
Marie-Dominique GalibertUniv Rennes, CNRS, IGDR (Institute of Genetics and Development of Rennes) - UMR 6290, Rennes, France.ORCID 0000-0003-0095-742X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The COVID-19 crisis and the development of the first approved mRNA vaccine have highlighted the power of RNA-based therapeutic strategies for the development of new medicines. Aside from RNA-vaccines, antisense oligonucleotides (ASOs) represent a new and very promising class of RNA-targeted therapy. Few drugs have already received approval from the Food and Drug Administration. Here, we underscored why and how ASOs hold the potential to change the therapeutic landscape to beat SARS-CoV-2 viral infections. This article is categorized under: RNA Interactions with Proteins and Other Molecules > Small Molecule-RNA Interactions.

Indexed as

COVID-19 Drug TreatmentOligonucleotides, AntisenseHumansmRNA VaccinesOligonucleotidesRNASARS-CoV-2United StatesVaccines, SyntheticmRNA VaccinesOligonucleotidesOligonucleotides, AntisenseRNAVaccines, Syntheticantisense oligonucleotideASOSARS-CoV-2therapeutic option

Identifiers

PMID34842345
PMCPMC9011570

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.