Evidence map›Paper›PMID 36809189›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2023

Mucociliary clearance augmenting drugs block SARS-CoV-2 replication in human airway epithelial cells.

Javier Campos-Gómez, Courtney Fernandez Petty, Marina Mazur, Liping Tang, George M Solomon, Reny Joseph, Qian Li, Jacelyn E Peabody Lever, Shah Saddad Hussain, Kevin S Harrod and 3 more

Open access · hybridFull text read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Interplay between respiratory viruses and cilia in the airways.European respiratory review : an official journal of the European Respiratory Society · 2025
    Review
  3. iScience · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 1 institution in 1 country.

Javier Campos-GómezDepartment of Medicine, University of Alabama at Birmingham, Alabama, United States.ORCID 0000-0002-2693-0885
Courtney Fernandez PettyDepartment of Medicine, University of Alabama at Birmingham, Alabama, United States.
Marina MazurDepartment of Medicine, University of Alabama at Birmingham, Alabama, United States.
Liping TangDepartment of Medicine, University of Alabama at Birmingham, Alabama, United States.
George M SolomonDepartment of Medicine, University of Alabama at Birmingham, Alabama, United States.ORCID 0000-0002-2969-5518
Reny JosephDepartment of Medicine, University of Alabama at Birmingham, Alabama, United States.
Qian LiDepartment of Medicine, University of Alabama at Birmingham, Alabama, United States.
Jacelyn E Peabody LeverDepartment of Medicine, University of Alabama at Birmingham, Alabama, United States.ORCID 0000-0003-3490-8474
Shah Saddad HussainDepartment of Medicine, University of Alabama at Birmingham, Alabama, United States.ORCID 0000-0002-6830-2924
Kevin S HarrodDepartment of Medicine, University of Alabama at Birmingham, Alabama, United States.
Ezinwanne E OnuohaDepartment of Biomedical Engineering, University of Alabama at Birmingham, Alabama, United States.ORCID 0000-0002-7744-0069
Harrison KimDepartment of Radiology, University of Alabama at Birmingham, Alabama, United States.ORCID 0000-0002-9126-1964
Steven M RoweDepartment of Medicine, University of Alabama at Birmingham, Alabama, United States.ORCID 0000-0001-9045-0133
University of Alabama at Birmingham · US

Funding

UAB CF Research and Translation Core CenterP30DK072482 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI AMIT GAGGAR · 2007 to 2026
$23.0M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM008361 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI YACOUBIAN, TALENE ALENE · 1992 to 2024
$16.8M
Translational Program in CFTR-Related Airway DiseasesR35HL135816 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ROWE, STEVEN MARK · 2017 to 2022
$6.3M
Training Program in Lung Biology and Translational MedicineT32HL105346 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GAGGAR, AMIT · 2010 to 2025
$5.0M
Mucus Matters: Mucociliary Physiology in Pulmonary FibrosisF31HL146083 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LEVER, JACELYN EMILY PEABODY · 2019 to 2020
$77k
NHLBI NIH HHS F31 HL146083NHLBI NIH HHS R35 HL135816NHLBI NIH HHS T32 HL105346NIDDK NIH HHS P30 DK072482NIGMS NIH HHS T32 GM008361
6 · The paper itself

Abstract

The coronavirus disease (COVID-19) pandemic, caused by SARS-CoV-2 coronavirus, is devastatingly impacting human health. A prominent component of COVID-19 is the infection and destruction of the ciliated respiratory cells, which perpetuates dissemination and disrupts protective mucociliary transport (MCT) function, an innate defense of the respiratory tract. Thus, drugs that augment MCT could improve the barrier function of the airway epithelium and reduce viral replication and, ultimately, COVID-19 outcomes. We tested five agents known to increase MCT through distinct mechanisms for activity against SARS-CoV-2 infection using a model of human respiratory epithelial cells terminally differentiated in an air/liquid interphase. Three of the five mucoactive compounds tested showed significant inhibitory activity against SARS-CoV-2 replication. An archetype mucoactive agent, ARINA-1, blocked viral replication and therefore epithelial cell injury; thus, it was further studied using biochemical, genetic, and biophysical methods to ascertain the mechanism of action via the improvement of MCT. ARINA-1 antiviral activity was dependent on enhancing the MCT cellular response, since terminal differentiation, intact ciliary expression, and motion were required for ARINA-1-mediated anti-SARS-CoV2 protection. Ultimately, we showed that the improvement of cilia movement was caused by ARINA-1-mediated regulation of the redox state of the intracellular environment, which benefited MCT. Our study indicates that intact MCT reduces SARS-CoV-2 infection, and its pharmacologic activation may be effective as an anti-COVID-19 treatment.

Indexed as

COVID-19SARS-CoV-2Epithelial CellsHumansMucociliary ClearanceRespiratory SystemVirus Replicationantioxidantcilia movementmucoactive drugmucociliary transportSARS-CoV-2

Identifiers

PMID36809189
PMCPMC10042606
OpenAlexW4321446605

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read55
identifiers read4
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.