Evidence map›Paper›PMID 35637239›Full record

ArticleScientific reports2022

Improved in-vivo airway gene transfer via magnetic-guidance, with protocol development informed by synchrotron imaging.

Martin Donnelley, Patricia Cmielewski, Kaye Morgan, Juliette Delhove, Nicole Reyne, Alexandra McCarron, Nathan Rout-Pitt, Victoria Drysdale, Chantelle Carpentieri, Kathryn Spiers and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 53% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

14 authors at 5 institutions in 3 countries.

Martin DonnelleyRobinson Research Institute, University of Adelaide, Adelaide, SA, 5001, Australia. martin.donnelley@adelaide.edu.au.
Patricia CmielewskiRobinson Research Institute, University of Adelaide, Adelaide, SA, 5001, Australia.
Kaye MorganSchool of Physics and Astronomy, Monash University, Clayton, VIC, 3800, Australia.
Juliette DelhoveRobinson Research Institute, University of Adelaide, Adelaide, SA, 5001, Australia.
Nicole ReyneRobinson Research Institute, University of Adelaide, Adelaide, SA, 5001, Australia.
Alexandra McCarronRobinson Research Institute, University of Adelaide, Adelaide, SA, 5001, Australia.
Nathan Rout-PittRobinson Research Institute, University of Adelaide, Adelaide, SA, 5001, Australia.
Victoria DrysdaleRobinson Research Institute, University of Adelaide, Adelaide, SA, 5001, Australia.
Chantelle CarpentieriRobinson Research Institute, University of Adelaide, Adelaide, SA, 5001, Australia.
Kathryn SpiersDeutsches Elektronen-Synchrotron DESY, Notkestr. 85, 22607, Hamburg, Germany.
Akihisa TakeuchiSPring-8 Synchrotron, Japan Synchrotron Radiation Institute, Kouto, Hyogo, Japan.
Kentaro UesugiSPring-8 Synchrotron, Japan Synchrotron Radiation Institute, Kouto, Hyogo, Japan.
Naoto YagiSPring-8 Synchrotron, Japan Synchrotron Radiation Institute, Kouto, Hyogo, Japan.
David ParsonsRobinson Research Institute, University of Adelaide, Adelaide, SA, 5001, Australia.
University of Adelaide · AUJapan Synchrotron Radiation Research Institute · JPWomen's and Children's Hospital · AUDeutsches Elektronen-Synchrotron DESY · DEMonash University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gene vectors to treat cystic fibrosis lung disease should be targeted to the conducting airways, as peripheral lung transduction does not offer therapeutic benefit. Viral transduction efficiency is directly related to the vector residence time. However, delivered fluids such as gene vectors naturally spread to the alveoli during inspiration, and therapeutic particles of any form are rapidly cleared via mucociliary transit. Extending gene vector residence time within the conducting airways is important, but hard to achieve. Gene vector conjugated magnetic particles that can be guided to the conducting airway surfaces could improve regional targeting. Due to the challenges of in-vivo visualisation, the behaviour of such small magnetic particles on the airway surface in the presence of an applied magnetic field is poorly understood. The aim of this study was to use synchrotron imaging to visualise the in-vivo motion of a range of magnetic particles in the trachea of anaesthetised rats to examine the dynamics and patterns of individual and bulk particle behaviour in-vivo. We also then assessed whether lentiviral-magnetic particle delivery in the presence of a magnetic field increases transduction efficiency in the rat trachea. Synchrotron X-ray imaging revealed the behaviour of magnetic particles in stationary and moving magnetic fields, both in-vitro and in-vivo. Particles could not easily be dragged along the live airway surface with the magnet, but during delivery deposition was focussed within the field of view where the magnetic field was the strongest. Transduction efficiency was also improved six-fold when the lentiviral-magnetic particles were delivered in the presence of a magnetic field. Together these results show that lentiviral-magnetic particles and magnetic fields may be a valuable approach for improving gene vector targeting and increasing transduction levels in the conducting airways in-vivo.

Indexed as

Genetic TherapySynchrotronsAnimalsMagneticsRatsTracheaX-Rays

Identifiers

PMID35637239
PMCPMC9151774
OpenAlexW4281732174

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.