Evidence map›Paper›PMID 35695453›Full record

ArticlemBio2022

Potency of Fusion-Inhibitory Lipopeptides against SARS-CoV-2 Variants of Concern.

Katharina S Schmitz, Daryl Geers, Rory D de Vries, T Francesca Bovier, Anna Z Mykytyn, Corine H Geurts van Kessel, Bart L Haagmans, Matteo Porotto, Rik L de Swart, Anne Moscona

Open access · goldAbstract read
In one paragraph

Article in mBio, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  8. Advancements in the Development of Anti-SARS-CoV-2 Therapeutics.International journal of molecular sciences · 2024
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Small molecules in the treatment of COVID-19.Signal transduction and targeted therapy · 2022
    Review
  16. 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 at 3 institutions in 3 countries.

Katharina S SchmitzDepartment Viroscience, Erasmus MCgrid.5645.2, Rotterdam, the Netherlands.ORCID 0000-0002-8537-0646
Daryl GeersDepartment Viroscience, Erasmus MCgrid.5645.2, Rotterdam, the Netherlands.
Rory D de VriesDepartment Viroscience, Erasmus MCgrid.5645.2, Rotterdam, the Netherlands.ORCID 0000-0003-2817-0127
T Francesca BovierDepartment of Pediatrics, Columbia University Vagelos College of Physicians & Surgeons, New York, New York, USA.
Anna Z MykytynDepartment Viroscience, Erasmus MCgrid.5645.2, Rotterdam, the Netherlands.
Corine H Geurts van KesselDepartment Viroscience, Erasmus MCgrid.5645.2, Rotterdam, the Netherlands.ORCID 0000-0002-7678-314X
Bart L HaagmansDepartment Viroscience, Erasmus MCgrid.5645.2, Rotterdam, the Netherlands.ORCID 0000-0001-6221-2015
Matteo PorottoDepartment of Pediatrics, Columbia University Vagelos College of Physicians & Surgeons, New York, New York, USA.ORCID 0000-0003-3866-9220
Rik L de SwartDepartment Viroscience, Erasmus MCgrid.5645.2, Rotterdam, the Netherlands.ORCID 0000-0003-3599-8969
Anne MosconaDepartment of Pediatrics, Columbia University Vagelos College of Physicians & Surgeons, New York, New York, USA.ORCID 0000-0002-1796-8320
Erasmus MC · NLColumbia University · USUniversity of Campania "Luigi Vanvitelli" · IT

Funding

Engineering protease-resistant antiviral peptide inhibitors for SARS-CoV-2R01AI160961 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MOSCONA, ANNE · 2021 to 2025
$3.6M
Fusion inhibitors that block host-to-host transmission of SARS-CoV-2R01AI160953 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI POROTTO, MATTEO · 2021 to 2025
$3.6M
NIAID NIH HHS R01 AI160953NIAID NIH HHS R01 AI160961
6 · The paper itself

Abstract

The ability of SARS-CoV-2 to evolve in response to selective pressures poses a challenge to vaccine and antiviral efficacy. The S1 subunit of the spike (S) protein contains the receptor-binding domain and is therefore under selective pressure to evade neutralizing antibodies elicited by vaccination or infection. In contrast, the S2 subunit of S is only transiently exposed after receptor binding, which makes it a less efficient target for antibodies. As a result, S2 has a lower mutational frequency than S1. We recently described monomeric and dimeric SARS-CoV-2 fusion-inhibitory lipopeptides that block viral infection by interfering with S2 conformational rearrangements during viral entry. Importantly, a dimeric lipopeptide was shown to block SARS-CoV-2 transmission between ferrets

Indexed as

COVID-19SARS-CoV-2AnimalsAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralFerretsHumansLipopeptidesSpike Glycoprotein, CoronavirusAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralLipopeptidesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2fusion inhibitorpostvaccine seraSARS-CoV-2Spike proteinviral evolution

Identifiers

PMID35695453
PMCPMC9239157
OpenAlexW4282836344

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.