Evidence map›Paper›PMID 40486909›Full record

ArticleFrontiers in cell and developmental biology2025

Cell-based high-content approach for SARS-CoV-2 neutralization identifies unique monoclonal antibodies and PI3K pathway inhibitors.

Carly R Cabel, Briana A Guzman, Elaheh Alizadeh, Shuaizhi Li, Cameron Holberg, Chonlarat Wichaidit, Darren A Cusanovich, Andrew L Paek, Gregory R J Thatcher, Koenraad Van Doorslaer and 7 more

Abstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2025. 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. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors.

Carly R CabelDepartment of Cellular and Molecular Medicine, University of Arizona, Tucson, AZ, United States.
Briana A GuzmanDepartment of Cellular and Molecular Medicine, University of Arizona, Tucson, AZ, United States.
Elaheh AlizadehDepartment of Cellular and Molecular Medicine, University of Arizona, Tucson, AZ, United States.
Shuaizhi LiDepartment of Immunobiology, BIO5 Institute, University of Arizona, Tucson, AZ, United States.
Cameron HolbergDepartment of Pharmacology & Toxicology, R. Ken Coit College of Pharmacy, University of Arizona, Tucson, AZ, United States.
Chonlarat WichaiditDepartment of Cellular and Molecular Medicine, University of Arizona, Tucson, AZ, United States.
Darren A CusanovichDepartment of Cellular and Molecular Medicine, University of Arizona, Tucson, AZ, United States.
Andrew L PaekCancer Biology Graduate Interdisciplinary Program, The University of Arizona, Tucson, AZ, United States.
Gregory R J ThatcherDepartment of Pharmacology & Toxicology, R. Ken Coit College of Pharmacy, University of Arizona, Tucson, AZ, United States.
Koenraad Van DoorslaerDepartment of Cellular and Molecular Medicine, University of Arizona, Tucson, AZ, United States.
Rachel S NargiVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN, United States.
Rachel E SuttonVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN, United States.
Naveenchandra SuryadevaraVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN, United States.
James E CroweVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN, United States.
Robert H CarnahanVanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, TN, United States.
Samuel K CamposCancer Biology Graduate Interdisciplinary Program, The University of Arizona, Tucson, AZ, United States.
Curtis A ThorneDepartment of Cellular and Molecular Medicine, University of Arizona, Tucson, AZ, United States.

Funding

Defining signaling networks in epithelial homeostasisR35GM147128 · NIGMS · UNIVERSITY OF ARIZONA · PI Curtis Andrew Thorne · 2022 to 2026
$2.0M
Beyond Pseudotime: Enhanced Single-cell Genomics Tools for Understanding the Temporal Dynamics of Development and DiseaseR35GM137896 · NIGMS · UNIVERSITY OF ARIZONA · PI CUSANOVICH, DARREN A · 2020 to 2024
$1.8M
NIGMS NIH HHS R35 GM137896NIGMS NIH HHS R35 GM147128
6 · The paper itself

Abstract

The sudden rise of the SARS-CoV-2 virus and the delay in development of effective therapeutics for mitigation made evident a need for ways to screen compounds that can block infection and prevent further pathogenesis and spread. However, identifying effective drugs that are efficacious against viral infection and replication with minimal toxicity for the patient can be difficult. Monoclonal antibodies were shown to be effective, but as the SARS-CoV-2 mutated, these antibodies became ineffective. Small-molecule antivirals were identified using pseudovirus constructs to recapitulate infection in nonhuman cells, such as Vero E6 cells. However, the impact was limited due to poor translation of these compounds in the clinical setting. This is partly due to the lack of similarity of screening platforms to the

Indexed as

COVIDdrug repurposingHCAHTSPI3K-AKT pathway

Identifiers

PMID40486909
PMCPMC12142043

What OpenQuestion holds

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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.