Evidence map›Paper›PMID 37880340›Full record

ArticleScientific reports2023

Development and qualification of clinical grade decellularized and cryopreserved human esophagi.

William Godefroy, Lionel Faivre, Caroline Sansac, Briac Thierry, Jean-Marc Allain, Patrick Bruneval, Rémy Agniel, Sabrina Kellouche, Olivier Monasson, Elisa Peroni and 10 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Ex vivo assay for organ-specific cancer cell invasion.Journal of biological engineering · 2026
    Article
  2. Article
  3. Article
  4. 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

20 authors at 8 institutions in 3 countries.

William GodefroyService de Chirurgie Viscérale, Cancérologique et Endocrinienne, Hôpital Saint-Louis - Université Paris Cité, Paris, France. william.godefroy@aphp.fr.
Lionel FaivreUnité de Thérapie Cellulaire, Hôpital Saint-Louis, AP-HP, Paris, France.
Caroline SansacBanque de Tissus Humains, Hôpital St-Louis, AP-HP, Paris, France.
Briac ThierryHuman Immunology, Pathophysiology, Immunotherapy / HIPI / INSERM UMR976, Laboratoire de Biotechnologies de Cellules Souches, Université Paris Cité, 75010, Paris, France.
Jean-Marc AllainLMS, CNRS, Ecole Polytechnique, Institut Polytechnique de Paris, Palaiseau, France.
Patrick BrunevalService d'Anatomie Pathologie, Hôpital Européen Georges Pompidou, AP-HP, Paris, France.
Rémy AgnielEquipe de Recherche sur les Relations Matrice Extracellulaire-Cellules, ERRMECe (EA1391), Institut des Matériaux, I-MAT (FD4122), CY Cergy Paris Université, Cergy-Pontoise, France.
Sabrina KelloucheEquipe de Recherche sur les Relations Matrice Extracellulaire-Cellules, ERRMECe (EA1391), Institut des Matériaux, I-MAT (FD4122), CY Cergy Paris Université, Cergy-Pontoise, France.
Olivier MonassonCNRS, BioCIS, CY Cergy Paris Université, 95000, Cergy Pontoise, France.
Elisa PeroniCNRS, BioCIS, CY Cergy Paris Université, 95000, Cergy Pontoise, France.
Mohamed JarrayaBanque de Tissus Humains, Hôpital St-Louis, AP-HP, Paris, France.
Niclas SetterbladUMS Saint-Louis US53 / UAR2030, Institut de Recherche Saint-Louis Plateforme Technologique Centre, Université Paris Cité - Inserm - CNRS, Paris, France.
Massymissa BraikUnité de Thérapie Cellulaire, Hôpital Saint-Louis, AP-HP, Paris, France.
Benjamin EvenLaboratoire Gly-CRRET, Université Paris Est Créteil, Université Paris Est, EA 4397 ERL CNRS 9215, Créteil, France.
Sophie CheverryLaboratoire Gly-CRRET, Université Paris Est Créteil, Université Paris Est, EA 4397 ERL CNRS 9215, Créteil, France.
Thomas DometUnité de Thérapie Cellulaire, Hôpital Saint-Louis, AP-HP, Paris, France.
Patricia AlbaneseLaboratoire Gly-CRRET, Université Paris Est Créteil, Université Paris Est, EA 4397 ERL CNRS 9215, Créteil, France.
Jérôme LargheroUnité de Thérapie Cellulaire, Hôpital Saint-Louis, AP-HP, Paris, France.
Pierre CattanService de Chirurgie Viscérale, Cancérologique et Endocrinienne, Hôpital Saint-Louis - Université Paris Cité, Paris, France.
Lousineh ArakelianUnité de Thérapie Cellulaire, Hôpital Saint-Louis, AP-HP, Paris, France. lousineh.arakelian@aphp.fr.
Assistance Publique – Hôpitaux de Paris · FRCentre National de la Recherche Scientifique · FRUniversité Paris-Est Créteil · FRCY Cergy Paris Université · FRUniversité Paris Cité · FRUniversité Paris-Saclay · FRHôpital Européen Georges-Pompidou · FRHôpital Necker-Enfants Malades · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tissue engineering is a promising alternative to current full thickness circumferential esophageal replacement methods. The aim of our study was to develop a clinical grade Decellularized Human Esophagus (DHE) for future clinical applications. After decontamination, human esophagi from deceased donors were placed in a bioreactor and decellularized with sodium dodecyl sulfate (SDS) and ethylendiaminetetraacetic acid (EDTA) for 3 days. The esophagi were then rinsed in sterile water and SDS was eliminated by filtration on an activated charcoal cartridge for 3 days. DNA was removed by a 3-hour incubation with DNase. A cryopreservation protocol was evaluated at the end of the process to create a DHE cryobank. The decellularization was efficient as no cells and nuclei were observed in the DHE. Sterility of the esophagi was obtained at the end of the process. The general structure of the DHE was preserved according to immunohistochemical and scanning electron microscopy images. SDS was efficiently removed, confirmed by a colorimetric dosage, lack of cytotoxicity on Balb/3T3 cells and mesenchymal stromal cell long term culture. Furthermore, DHE did not induce lymphocyte proliferation in-vitro. The cryopreservation protocol was safe and did not affect the tissue, preserving the biomechanical properties of the DHE. Our decellularization protocol allowed to develop the first clinical grade human decellularized and cryopreserved esophagus.

Indexed as

Extracellular MatrixTissue ScaffoldsAnimalsCryopreservationEsophagusHumansMiceSodium Dodecyl SulfateTissue EngineeringSodium Dodecyl Sulfate

Identifiers

PMID37880340
PMCPMC10600094
OpenAlexW4387936916

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.