Evidence map›Paper›PMID 37382374›Full record

ArticleLaboratory animals2023

A minimally invasive bronchoscopic approach for direct delivery to murine airways and application to models of pulmonary infection.

Karen Schelde, Julie Rosenjack, Claire Sonneborn, Anjum Jafri, Michael Kavran, Sarah Brumbaugh, Arne Rietsch, Rebecca J Darrah, Craig A Hodges, Christopher A Flask and 2 more

Abstract read
In one paragraph

Article in Laboratory animals, 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
–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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

12 authors.

Karen ScheldeDepartment of Genetics and Genome Sciences, Case Western Reserve University, USA.ORCID 0000-0002-7162-6938
Julie RosenjackDepartment of Genetics and Genome Sciences, Case Western Reserve University, USA.
Claire SonnebornDepartment of Genetics and Genome Sciences, Case Western Reserve University, USA.
Anjum JafriDepartment of Genetics and Genome Sciences, Case Western Reserve University, USA.
Michael KavranDepartment of Radiology, University Hospitals Cleveland Medical Center, USA.
Sarah BrumbaughCleveland Institute of Art, USA.
Arne RietschDepartment of Molecular Biology and Microbiology, Case Western Reserve University, USA.
Rebecca J DarrahDepartment of Genetics and Genome Sciences, Case Western Reserve University, USA.
Craig A HodgesDepartment of Genetics and Genome Sciences, Case Western Reserve University, USA.
Christopher A FlaskDepartment of Radiology, University Hospitals Cleveland Medical Center, USA.
Thomas J KelleyDepartment of Genetics and Genome Sciences, Case Western Reserve University, USA.
Mitchell L DrummDepartment of Genetics and Genome Sciences, Case Western Reserve University, USA.ORCID 0000-0003-4739-5153

Funding

TUMOR METABOLISM PROGRAMP30CA043703 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI Amar Desai · 1987 to 2026
$142.3M
Clinical and Translational Science Collaborative of ClevelandUL1TR002548 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI MCCOMSEY, GRACE A · 2018 to 2022
$35.5M
Clinical and Translational Science Collaborative of Northern Ohio, Catalyzing Linkages to Equity in Health (CLE Health)UM1TR004528 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI GRACE A MCCOMSEY · 2023 to 2026
$32.1M
The Cleveland Digestive Diseases Research Core Center (DDRCC)P30DK097948 · NIDDK · CASE WESTERN RESERVE UNIVERSITY · PI AMITABH CHAK · 2015 to 2026
$15.6M
NCATS NIH HHS UL1 TR002548NCATS NIH HHS UM1 TR004528NCI NIH HHS P30 CA043703NIDDK NIH HHS P30 DK097948
6 · The paper itself

Abstract

The laboratory mouse is used extensively for human disease modeling and preclinical therapeutic testing for efficacy, biodistribution, and toxicity. The variety of murine models available, and the ability to create new ones, eclipses all other species, but the size of mice and their organs create challenges for many in vivo studies. For pulmonary research, improved methods to access murine airways and lungs, and track substances administered to them, would be desirable. A nonsurgical endoscopic system with a camera, effectively a bronchoscope, coupled with a cryoimaging fluorescence microscopy technique to view the lungs in 3D, is described here that allows visualization of the procedure, including the anatomical location at which substances are instilled and fluorescence detection of those substances. We have applied it to bacterial infection studies to characterize better and optimize a chronic lung infection murine model in which we instill bacteria-laden agarose beads into the airways and lungs to extend the duration of the infection and inflammation. The use of the endoscope as guidance for placing a catheter into the airways is simple and quick, requiring only momentary sedation, and reduces post-procedural mortality compared with our previous instillation method that includes a trans-tracheal surgery. The endoscopic method improves speed and precision of delivery while reducing the stress on animals and the number of animals generated and used for experiments.

Indexed as

BronchoscopyLungAnimalsHumansMiceTissue DistributionBronchoscopyethics and welfarelung infectionreductionrefinement

Identifiers

PMID37382374
PMCPMC10693731

What OpenQuestion holds

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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.