Evidence map›Paper›PMID 34798263›Full record

ArticlePharmacological research2022

DNA aptamers masking angiotensin converting enzyme 2 as an innovative way to treat SARS-CoV-2 pandemic.

Alessandro Villa, Electra Brunialti, Jessica Dellavedova, Clara Meda, Monica Rebecchi, Matteo Conti, Lorena Donnici, Raffaele De Francesco, Angelo Reggiani, Vincenzo Lionetti and 1 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Pharmacological research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Association of COVID-19 with Comorbidities: An Update.ACS pharmacology & translational science · 2023
    Review
  6. Aptamer-Based Strategies to Address Challenges in COVID-19 Diagnosis and Treatments.Interdisciplinary perspectives on infectious diseases · 2023
    Review
  7. The Spike Mutants Website: A Worldwide Used Resource against SARS-CoV-2.International journal of molecular sciences · 2022
    Article
  8. Review
  9. Label-free optical biosensors in the pandemic era.Nanophotonics (Berlin, Germany) · 2022
    Review
  10. Review
  11. Article
  12. Aptamers-Diagnostic and Therapeutic Solution in SARS-CoV-2.International journal of molecular sciences · 2022
    Review
  13. Article
  14. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

Alessandro VillaDepartment of Health Sciences, University of Milan, Milan 20146, Italy.
Electra BrunialtiDepartment of Health Sciences, University of Milan, Milan 20146, Italy.
Jessica DellavedovaDepartment of Health Sciences, University of Milan, Milan 20146, Italy.
Clara MedaDepartment of Health Sciences, University of Milan, Milan 20146, Italy.
Monica RebecchiDepartment of Health Sciences, University of Milan, Milan 20146, Italy.
Matteo ContiINGM - Istituto Nazionale Genetica Molecolare "Romeo ed Enrica Invernizzi", Milan 20122, Italy.
Lorena DonniciINGM - Istituto Nazionale Genetica Molecolare "Romeo ed Enrica Invernizzi", Milan 20122, Italy.
Raffaele De FrancescoINGM - Istituto Nazionale Genetica Molecolare "Romeo ed Enrica Invernizzi", Milan 20122, Italy; Department of Pharmacological and Biomolecular Sciences, University of Milan, Milan 20133, Italy.
Angelo ReggianiD3 Validation Research Line, Istituto Italiano di Tecnologia, Genoa 16163, Italy.
Vincenzo LionettiInstitute of Life Sciences, Scuola Superiore Sant'Anna, Pisa 56127, Italy.
Paolo CianaD3 Validation Research Line, Istituto Italiano di Tecnologia, Genoa 16163, Italy. Electronic address: paolo.ciana@unimi.it.
University of Milan · ITIstituto Nazionale Genetica Molecolare · ITItalian Institute of Technology · ITScuola Superiore Sant'Anna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

All the different coronavirus SARS-CoV-2 variants isolated so far share the same mechanism of infection mediated by the interaction of their spike (S) glycoprotein with specific residues on their cellular receptor: the angiotensin converting enzyme 2 (ACE2). Therefore, the steric hindrance on this cellular receptor created by a bulk macromolecule may represent an effective strategy for the prevention of the viral spreading and the onset of severe forms of Corona Virus disease 19 (COVID-19). Here, we applied a systematic evolution of ligands by exponential enrichment (SELEX) procedure to identify two single strand DNA molecules (aptamers) binding specifically to the region surrounding the K353, the key residue in human ACE2 interacting with the N501 amino acid of the SARS-CoV-2 S. 3D docking in silico experiments and biochemical assays demonstrated that these aptamers bind to this region, efficiently prevent the SARS-CoV-2 S/human ACE2 interaction and the viral infection in the nanomolar range, regardless of the viral variant, thus suggesting the possible clinical development of these aptamers as SARS-CoV-2 infection inhibitors. Our approach brings a significant innovation to the therapeutic paradigm of the SARS-CoV-2 pandemic by protecting the target cell instead of focusing on the virus; this is particularly attractive in light of the increasing number of viral mutants that may potentially escape the currently developed immune-mediated neutralization strategies.

Indexed as

COVID-19 Drug TreatmentA549 CellsAngiotensin-Converting Enzyme 2Aptamers, NucleotideCOVID-19HEK293 CellsHost-Pathogen InteractionsHumansMutationReceptors, VirusSARS-CoV-2SELEX Aptamer TechniqueVirus InternalizationACE2 protein, humanAce2 protein, mouseAngiotensin-Converting Enzyme 2Aptamers, NucleotideReceptors, VirusACE2CoronavirusCOVID-19 therapyNucleic acid-based drugsSARS-CoV-2 variants

Identifiers

PMID34798263
PMCPMC8594078
OpenAlexW3212672606

What OpenQuestion holds

Textmetadata
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.