Evidence map›Paper›PMID 34961486›Full record

ReviewMolecular medicine (Cambridge, Mass.)2021

Perspectives and potential approaches for targeting neuropilin 1 in SARS-CoV-2 infection.

Svetlana P Chapoval, Achsah D Keegan

Open access · goldAbstract readReview
In one paragraph

Review in Molecular medicine (Cambridge, Mass.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 18% 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, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Biophysical investigation of interactions between SARS-CoV-2 spike protein and neuropilin-1.Protein science : a publication of the Protein Society · 2023
    Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. The role of DC-SIGN as a trans-receptor in infection by MERS-CoV.Frontiers in cellular and infection microbiology · 2023
    Article
  14. 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

2 authors at 2 institutions in 1 country.

Svetlana P ChapovalDepartment of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, MD, USA. schapoval@som.umaryland.edu.ORCID 0000-0002-7590-4421
Achsah D KeeganDepartment of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, MD, USA.
University of Mary · USUniversity of Maryland, Baltimore · US

Funding

IL-4-activated macrophages: Contribution to allergic lung inflammation linked to viral infectionR01AI143845 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI KEEGAN, ACHSAH D., VISCARDI, ROSE MARIE · 2019 to 2023
$3.1M
Role of Semaphorin 4A in Allergic InflammationR01AI122631 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI KEEGAN, ACHSAH D. · 2018 to 2022
$1.9M
Immune Semaphorins in Allergic Airway InflammationR21AI076736 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI CHAPOVAL, SVETLANA P. · 2009 to 2010
$413k
Regulation of Macrophage Activation by House Dust MiteI01BX001850 · VA · BALTIMORE VA MEDICAL CENTER · PI KEEGAN, ACHSAH D. · 2013 to 2022
–
BLRD VA I01 BX001850National Institute of Allergy and Infectious Diseases RO1 AI076736NIAID NIH HHS R01 AI122631NIAID NIH HHS R01 AI143845
6 · The paper itself

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a novel type b coronavirus responsible for the COVID-19 pandemic. With over 224 million confirmed infections with this virus and more than 4.6 million people dead because of it, it is critically important to define the immunological processes occurring in the human response to this virus and pathogenetic mechanisms of its deadly manifestation. This perspective focuses on the contribution of the recently discovered interaction of SARS-CoV-2 Spike protein with neuropilin 1 (NRP1) receptor, NRP1 as a virus entry receptor for SARS-CoV-2, its role in different physiologic and pathologic conditions, and the potential to target the Spike-NRP1 interaction to combat virus infectivity and severe disease manifestations.

Indexed as

COVID-19 Drug TreatmentAngiotensin-Converting Enzyme 2Antiviral AgentsComorbidityCOVID-19Diabetes MellitusFemaleHost-Pathogen InteractionsHumansInfantMolecular Targeted TherapyNeuropilin-1PregnancyPregnancy Complications, InfectiousSARS-CoV-2Spike Glycoprotein, CoronavirusACE2 protein, humanAngiotensin-Converting Enzyme 2Antiviral AgentsNeuropilin-1NRP1 protein, humanSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2ACE2, angiotensin converting enzyme 2CendR C-end ruleComorbiditiesCOVID-19, coronavirus disease 2019Host immune responseImmunotargets and strategiesMolecular structuresNRP-1, neuropilin-1RBD, receptor-biding domainSARS-CoV-2, severe acute respiratory syndrome coronavirus 2Spike protein

Identifiers

PMID34961486
PMCPMC8711287
OpenAlexW4200560449

What Socratic 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 Socratic graph.