Evidence map›Paper›PMID 33324660›Full record

ArticleFrontiers in medicine2020

Beneficial Effect of Systemic Allogeneic Adipose Derived Mesenchymal Cells on the Clinical, Inflammatory and Immunologic Status of a Patient With Recessive Dystrophic Epidermolysis Bullosa: A Case Report.

Rocío Maseda, Lucía Martínez-Santamaría, Rosa Sacedón, Nora Butta, María Del Carmen de Arriba, Sara García-Barcenilla, Marta García, Nuria Illera, Isabel Pérez-Conde, Marta Carretero and 8 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. 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

18 authors at 7 institutions in 1 country.

Rocío MasedaDepartment of Dermatology, La Paz University Hospital, Madrid, Spain.
Lucía Martínez-SantamaríaDepartment of Bioengineering, Carlos III University (UC3M), Madrid, Spain.
Rosa SacedónDepartment of Cell Biology, Faculty of Medicine, Complutense University, Madrid, Spain.
Nora ButtaHematology Unit, La Paz University Hospital-IdiPAZ, Madrid, Spain.
María Del Carmen de ArribaDepartment of Bioengineering, Carlos III University (UC3M), Madrid, Spain.
Sara García-BarcenillaHematology Unit, La Paz University Hospital-IdiPAZ, Madrid, Spain.
Marta GarcíaDepartment of Bioengineering, Carlos III University (UC3M), Madrid, Spain.
Nuria IlleraRare Diseases Networking Biomedical Research Centre (CIBERER) U714, Madrid, Spain.
Isabel Pérez-CondeDepartment of Dermatology, La Paz University Hospital, Madrid, Spain.
Marta CarreteroRare Diseases Networking Biomedical Research Centre (CIBERER) U714, Madrid, Spain.
Eva JiménezDepartment of Cell Biology, Faculty of Medicine, Complutense University, Madrid, Spain.
Gustavo MelenCell & Gene Therapies Laboratory, Niño Jesus University Hospital, Madrid, Spain.
Alberto M BorobiaClinical Pharmacology Department, School of Medicine, La Paz University Hospital, IdiPAZ, Autonomous University of Madrid, Madrid, Spain.
Víctor Jiménez-YusteHematology Unit, La Paz University Hospital-IdiPAZ, Madrid, Spain.
Ángeles VicenteDepartment of Cell Biology, Faculty of Medicine, Complutense University, Madrid, Spain.
Marcela Del RíoDepartment of Bioengineering, Carlos III University (UC3M), Madrid, Spain.
Raúl de LucasDepartment of Dermatology, La Paz University Hospital, Madrid, Spain.
María José EscámezDepartment of Bioengineering, Carlos III University (UC3M), Madrid, Spain.
Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas · ESHospital Universitario La Paz · ESUniversidad Complutense de Madrid · ESCentre for Biomedical Network Research on Rare Diseases · ESHospital Infantil Universitario Niño Jesús · ESHospital Universitario Fundación Jiménez Díaz · ESUniversidad Autónoma de Madrid · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recessive dystrophic epidermolysis bullosa (RDEB) is an incurable inherited mucocutaneous fragility disorder characterized by recurrent blisters, erosions, and wounds. Continuous blistering triggers overlapping cycles of never-ending healing and scarring commonly evolving to chronic systemic inflammation and fibrosis. The systemic treatment with allogeneic mesenchymal cells (MSC) from bone marrow has previously shown benefits in RDEB. MSC from adipose tissue (ADMSC) are easier to isolate. This is the first report on the use of systemic allogeneic ADMSC, correlating the clinical, inflammatory, and immunologic outcomes in RDEB indicating long-lasting benefits. We present the case of an RDEB patient harboring heterozygous biallelic

Indexed as

adipose derived MSC (ADMSC)case reportinflammationmesenchymal stromal cells (MSC)recessive dystrophic epidermolysis bullosa (RDEB)systemic cell therapy

Identifiers

PMID33324660
PMCPMC7726418
OpenAlexW3110220546

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.