Evidence map›Paper›PMID 38761062›Full record

ArticleCell transplantation

Plasma-Based Scaffold Containing Bone-Marrow Mononuclear Cells Promotes Wound Healing in a Mouse Model of Pressure Injury.

Maria Alvarez-Viejo, Luis Romero-Rosal, Marcos Perez-Basterrechea, Jose M García-Gala, Pablo Hernando-Rodriguez, Jesus Marana-Gonzalez, Miriam Rubiera-Valdes, Blanca Vivanco-Allende, Angeles Fernandez-Rodriguez, Eva Martinez-Revuelta and 1 more

Abstract read
In one paragraph

Article in Cell transplantation. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

11 authors.

Maria Alvarez-ViejoUnit of Cell Therapy and Regenerative Medicine, Department of Hematology and Hemotherapy, Central University Hospital of Asturias, Oviedo, Spain.
Luis Romero-RosalDepartment of Plastic and Reconstructive Surgery, Central University Hospital of Asturias, Oviedo, Spain.
Marcos Perez-BasterrecheaUnit of Cell Therapy and Regenerative Medicine, Department of Hematology and Hemotherapy, Central University Hospital of Asturias, Oviedo, Spain.
Jose M García-GalaUnit of Cell Therapy and Regenerative Medicine, Department of Hematology and Hemotherapy, Central University Hospital of Asturias, Oviedo, Spain.
Pablo Hernando-RodriguezHealth Research Institute of the Principality of Asturias-Foundation for Biomedical Research and Innovation in Asturias, Oviedo, Spain.
Jesus Marana-GonzalezNuclear Medicine Unit, Leon University Healthcare Complex, Leon, Spain.
Miriam Rubiera-ValdesPathological Anatomy Service, Central University Hospital of Asturias, Oviedo, Spain.
Blanca Vivanco-AllendePathological Anatomy Service, Central University Hospital of Asturias, Oviedo, Spain.
Angeles Fernandez-RodriguezUnit of Cell Therapy and Regenerative Medicine, Department of Hematology and Hemotherapy, Central University Hospital of Asturias, Oviedo, Spain.
Eva Martinez-RevueltaUnit of Cell Therapy and Regenerative Medicine, Department of Hematology and Hemotherapy, Central University Hospital of Asturias, Oviedo, Spain.
Silvia Perez-LopezUnit of Cell Therapy and Regenerative Medicine, Department of Hematology and Hemotherapy, Central University Hospital of Asturias, Oviedo, Spain.ORCID 0000-0002-2418-2510

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pressure injuries, or pressure ulcers, are a common problem that may lead to infections and major complications, besides being a social and economic burden due to the costs of treatment and hospitalization. While surgery is sometimes necessary, this also has complications such as recurrence or wound dehiscence. Among the newer methods of pressure injury treatment, advanced therapies are an interesting option. This study examines the healing properties of bone marrow mononuclear cells (BM-MNCs) embedded in a plasma-based scaffold in a mouse model. Pressure ulcers were created on the backs of mice (2 per mouse) using magnets and assigned to a group of ulcers that were left untreated (Control, n = 15), treated with plasma scaffold (Plasma, n = 15), or treated with plasma scaffold containing BM-MNC (Plasma + BM-MNC, n = 15). Each group was examined at three time points (3, 7, and 14 days) after the onset of treatment. At each time point, animals were subjected to biometric assessment, bioluminescence imaging, and tomography. Once treatment had finished, skin biopsies were processed for histological and wound healing reverse transcription polymerase chain reaction (RT-PCR) array studies. While wound closure percentages were higher in the Plasma and Plasma + BM-MNC groups, differences were not significant, and thus descriptive data are provided. In all individuals, the presence of donor cells was revealed by immunohistochemistry on posttreatment onset Days 3, 7, and 14. In the Plasma + BM-MNC group, less inflammation was observed by positron emission tomography-computed tomography (PET/CT) imaging of the mice at 7 days, and a complete morphometabolic response was produced at 14 days, in accordance with histological results. A much more pronounced inflammatory process was observed in controls than in the other two groups, and this persisted until Day 14 after treatment onset. RT-PCR array gene expression patterns were also found to vary significantly, with the greatest difference noted between both treatments at 14 days when 11 genes were differentially expressed.

Indexed as

Bone Marrow CellsDisease Models, AnimalPressure UlcerWound HealingAnimalsBone Marrow TransplantationLeukocytes, MononuclearMaleMiceMice, Inbred C57BLTissue Scaffoldsadvanced therapiesbone-marrow mononuclear cellspressure injuryscaffoldwound healing

Identifiers

PMID38761062
PMCPMC11102697

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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.