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dc.contributor.authorSierra Sánchez, Álvaro
dc.contributor.authorMagne, Brice
dc.contributor.authorSavard, Etienne
dc.contributor.authorMartel, Christian
dc.contributor.authorFerland, Karel
dc.contributor.authorBarbier, Martin A.
dc.contributor.authorDemers, Anabelle
dc.contributor.authorLarouche, Danielle
dc.contributor.authorArias Santiago, Salvador Antonio 
dc.contributor.authorGermain, Lucie
dc.date.accessioned2026-01-22T11:14:45Z
dc.date.available2026-01-22T11:14:45Z
dc.date.issued2023
dc.identifier.citationSierra Sánchez, A.; Magne, B.; Savard, E.; [et al.]. (2023). In vitro comparison of human plasma-based and self-assembled tissue-engineered skin substitutes: two different manufacturing processes for the treatment of deep and difficult to heal injuries. Burns & Trauma, Volume 11, 2023, tkad043, https://doi.org/10.1093/burnst/tkad043es_ES
dc.identifier.issn2321-3876
dc.identifier.urihttps://hdl.handle.net/10481/110092
dc.descriptionThis study has been funded by the Instituto de Salud Carlos III through the project PI17/02083 (co-funded by the European Regional Development Fund “A way to make Europe”), the Regional Government of Andalusia (PIGE-0242-2019), the Canadian Institutes for Health Research (CIHR) (FDN-143213 and IC-132948), the Fondation des Pompiers du Québec pour les Grands Brûlés (FPQGB) and the Quebec Network for Cell, Tissue and Gene Therapy—ThéCell (a thematic network supported by the Fonds de Recherche du Québec—Santé [FRQS]). The work of Álvaro Sierra-Sánchez was supported by a predoctoral fellowship and a mobility aid funded by the Instituto de Salud Carlos III (co-funded by the European Social Fund “Investing in your future”) with the dossier numbers FI18/00269 and MV20/00043, respectively. This study is part of his doctoral research in the Biomedicine’s program of University of Granada. The work of Brice Magne was supported by a postdoctoral fellowship funded by the FRQS. Karel Ferland and Anabelle Demers were supported by a Master studentship funded by the FRQS. Lucie Germain is the recipient of a Tier 1 Canadian Research Chair in Stem Cells and Tissue Engineering and a Research Chair on Tissue-Engineered Organs and Translational Medicine from the Fondation de l’Université Laval.es_ES
dc.description.abstractBackground: The aim of this in vitro study was to compare side-by-side two models of human bilayered tissue-engineered skin substitutes (hbTESSs) designed for the treatment of severely burned patients. These are the scaffold-free self-assembled skin substitute (SASS) and the human plasma-based skin substitute (HPSS). Methods: Fibroblasts and keratinocytes from three humans were extracted from skin biopsies (N = 3) and cells from the same donor were used to produce both hbTESS models. For SASS manufacture, keratinocytes were seeded over three self-assembled dermal sheets comprising fibroblasts and the extracellular matrix they produced (n = 12), while for HPSS production, keratinocytes were cultured over hydrogels composed of fibroblasts embedded in either plasma as unique biomaterial (Fibrin), plasma combined with hyaluronic acid (Fibrin-HA) or plasma combined with collagen (Fibrin-Col) (n/biomaterial = 9). The production time was 46-55 days for SASSs and 32-39 days for HPSSs. Substitutes were characterized by histology, mechanical testing, PrestoBlue™-assay, immunofluorescence (Ki67, Keratin (K) 10, K15, K19, Loricrin, type IV collagen) and Western blot (type I and IV collagens). Results: The SASSs were more resistant to tensile forces (p-value < 0.01) but less elastic (p-value < 0.001) compared to HPSSs. A higher number of proliferative Ki67+ cells were found in SASSs although their metabolic activity was lower. After epidermal differentiation, no significant difference was observed in the expression of K10, K15, K19 and Loricrin. Overall, the production of type I and type IV collagens and the adhesive strength of the dermal-epidermal junction was higher in SASSs. Conclusions: This study demonstrates, for the first time, that both hbTESS models present similar in vitro biological characteristics. However, mechanical properties differ and future in vivo experiments will aim to compare their wound healing potential.es_ES
dc.description.sponsorshipInstituto de Salud Carlos III, PI17/02083es_ES
dc.description.sponsorshipRegional Government of Andalusia, PIGE-0242-2019es_ES
dc.description.sponsorshipCanadian Institutes for Health Research, FDN-143213 and IC-132948es_ES
dc.description.sponsorshipFondation des Pompiers du Québec pour les Grands Brûléses_ES
dc.description.sponsorshipInstituto de Salud Carlos III, FI18/00269 and MV20/00043es_ES
dc.language.isoenges_ES
dc.publisherOxford Academices_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectBiomaterialses_ES
dc.subjectBurnes_ES
dc.subjectFibrines_ES
dc.titleIn vitro comparison of human plasma-based and self-assembled tissue-engineered skin substitutes: two different manufacturing processes for the treatment of deep and difficult to heal injurieses_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.1093/burnst/tkad043
dc.type.hasVersionAMes_ES


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