Evidence map›Paper›PMID 29302362›Full record

ReviewNPJ Regenerative medicine2017

Preclinical imaging methods for assessing the safety and efficacy of regenerative medicine therapies.

Lauren Scarfe, Nathalie Brillant, J Dinesh Kumar, Noura Ali, Ahmed Alrumayh, Mohammed Amali, Stephane Barbellion, Vendula Jones, Marije Niemeijer, Sophie Potdevin and 30 more

Abstract readReview
In one paragraph

Review in NPJ Regenerative medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. X-Ray Visible Protein Scaffolds by Bulk Iodination.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Vulnerable Plaque, Characteristics, Detection, and Potential Therapies.Journal of cardiovascular development and disease · 2019
    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

40 authors.

Lauren Scarfe *Department of Cellular and Molecular Physiology, University of Liverpool, Liverpool, UK.
Nathalie Brillant *Department of Molecular and Clinical Pharmacology, University of Liverpool, Liverpool, UK.
J Dinesh Kumar *Department of Cellular and Molecular Physiology, University of Liverpool, Liverpool, UK.
Noura AliCollege of Health Science, University of Duhok, Duhok, Iraq.
Ahmed AlrumayhDepartment of Molecular and Clinical Pharmacology, University of Liverpool, Liverpool, UK.
Mohammed AmaliDepartment of Molecular and Clinical Pharmacology, University of Liverpool, Liverpool, UK.
Stephane BarbellionMedical Research Council Centre for Drug Safety Science, University of Liverpool, Liverpool, UK.
Vendula JonesGlaxoSmithKline, David Jack Centre for Research and Development, Ware, UK.
Marije NiemeijerLeiden Academic Centre for Drug Research, Leiden University, Leiden, Netherlands.
Sophie PotdevinSANOFI Research and Development, Disposition, Safety and Animal Research, Alfortville, France.
Gautier RoussignolSANOFI Research and Development, Disposition, Safety and Animal Research, Alfortville, France.
Anatoly VaganovDepartment of Biology, University of Konstanz, Konstanz, Germany.
Ivana BarbaricDepartment of Biomedical Science, University of Sheffield, Sheffield, UK.
Michael BarrowDepartment of Chemistry, University of Liverpool, Liverpool, UK.
Neal C BurtoniThera Medical, Munich, Germany.
John ConnellCentre for Advanced Biomedical Imaging, University College London, London, UK.
Francesco DazziDepartment of Haemato-Oncology, King's College London, London, UK.
Josefina EdsbaggeTakara Bio Europe AB, Gothenburg, Sweden.
Neil S FrenchDepartment of Molecular and Clinical Pharmacology, University of Liverpool, Liverpool, UK.
Julie HolderRoslin Cells, University of Cambridge, Cambridge, UK.
Claire HutchinsonDepartment of Molecular and Clinical Pharmacology, University of Liverpool, Liverpool, UK.
David R JonesMedicines and Healthcare Products Regulatory Agency, London, UK.
Tammy KalberCentre for Advanced Biomedical Imaging, University College London, London, UK.
Cerys LovattGlaxoSmithKline, David Jack Centre for Research and Development, Ware, UK.
Mark F LythgoeCentre for Advanced Biomedical Imaging, University College London, London, UK.
Sara PatelReNeuron Ltd, Pencoed Business Park, Pencoed, Bridgend, UK.
P Stephen PatrickCentre for Advanced Biomedical Imaging, University College London, London, UK.ORCID 0000-0002-7155-1729
Jacqueline PinerGlaxoSmithKline, Medicines Research Centre, Gunnels Wood Road, Stevenage, UK.
Jens ReinhardtPaul Ehrlich Institut, Langen, Germany.
Emanuelle RicciInstitute of Veterinary Science, University of Liverpool, Liverpool, UK.
James SidawayPhenotox, Macclesfield, UK.
Glyn N StaceyUK Stem Cell Bank, Division of Advanced Therapies, National Institute for Biological Standards Control, Medicines and Healthcare Products Regulatory Agency, London, UK.
Philip J Starkey LewisMedical Research Council Centre for Regenerative Medicine, University of Edinburgh, Edinburgh, UK.
Gareth SullivanDepartment of Biochemistry, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Arthur TaylorDepartment of Cellular and Molecular Physiology, University of Liverpool, Liverpool, UK.
Bettina WilmDepartment of Cellular and Molecular Physiology, University of Liverpool, Liverpool, UK.
Harish PoptaniDepartment of Cellular and Molecular Physiology, University of Liverpool, Liverpool, UK.
Patricia MurrayDepartment of Cellular and Molecular Physiology, University of Liverpool, Liverpool, UK.
Chris E P GoldringDepartment of Molecular and Clinical Pharmacology, University of Liverpool, Liverpool, UK.
B Kevin ParkDepartment of Molecular and Clinical Pharmacology, University of Liverpool, Liverpool, UK.

Funding

Medical Research Council G0700654Medical Research Council MR/K026739/1
6 · The paper itself

Abstract

Regenerative medicine therapies hold enormous potential for a variety of currently incurable conditions with high unmet clinical need. Most progress in this field to date has been achieved with cell-based regenerative medicine therapies, with over a thousand clinical trials performed up to 2015. However, lack of adequate safety and efficacy data is currently limiting wider uptake of these therapies. To facilitate clinical translation, non-invasive in vivo imaging technologies that enable careful evaluation and characterisation of the administered cells and their effects on host tissues are critically required to evaluate their safety and efficacy in relevant preclinical models. This article reviews the most common imaging technologies available and how they can be applied to regenerative medicine research. We cover details of how each technology works, which cell labels are most appropriate for different applications, and the value of multi-modal imaging approaches to gain a comprehensive understanding of the responses to cell therapy in vivo.

Identifiers

PMID29302362
PMCPMC5677988

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.