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      Surgical Application of Human Amniotic Membrane and Amnion-Chorion Membrane in the Oral Cavity and Efficacy Evaluation: Corollary With Ophthalmological and Wound Healing Experiences

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          Abstract

          Due to its intrinsic properties, there has been growing interest in human amniotic membrane (hAM) in recent years particularly for the treatment of ocular surface disorders and for wound healing. Herein, we investigate the potential use of hAM and amnion-chorion membrane (ACM) in oral surgery. Based on our analysis of the literature, it appears that their applications are very poorly defined. There are two options: implantation or use as a cover material graft. The oral cavity is submitted to various mechanical and biological stimulations that impair membrane stability and maintenance. Thus, some devices have been combined with the graft to secure its positioning and protect it in this location. This current opinion paper addresses in detail suitable procedures for hAM and ACM utilization in soft and hard tissue reconstruction in the oral cavity. We address their implantation and/or use as a covering, storage format, application side, size and number, multilayer use or folding, suture or use of additional protective covers, re-application and resorption/fate. We gathered evidence on pre- and post-surgical care and evaluation tools. Finally, we integrated ophthalmological and wound healing practices into the collected information. This review aims to help practitioners and researchers better understand the application of hAM and ACM in the oral cavity, a place less easily accessible than ocular or cutaneous surfaces. Additionally, it could be a useful reference in the generation of new ideas for the development of innovative protective covering, suturing or handling devices in this specific indication. Finally, this overview could be considered as a position paper to guide investigators to fulfill all the identified criteria in the future.

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          Most cited references107

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          Concise review: isolation and characterization of cells from human term placenta: outcome of the first international Workshop on Placenta Derived Stem Cells.

          Placental tissue draws great interest as a source of cells for regenerative medicine because of the phenotypic plasticity of many of the cell types isolated from this tissue. Furthermore, placenta, which is involved in maintaining fetal tolerance, contains cells that display immunomodulatory properties. These two features could prove useful for future cell therapy-based clinical applications. Placental tissue is readily available and easily procured without invasive procedures, and its use does not elicit ethical debate. Numerous reports describing stem cells from different parts of the placenta, using nearly as numerous isolation and characterization procedures, have been published. Considering the complexity of the placenta, an urgent need exists to define, as clearly as possible, the region of origin and methods of isolation of cells derived from this tissue. On March 23-24, 2007, the first international Workshop on Placenta Derived Stem Cells was held in Brescia, Italy. Most of the research published in this area focuses on mesenchymal stromal cells isolated from various parts of the placenta or epithelial cells isolated from amniotic membrane. The aim of this review is to summarize and provide the state of the art of research in this field, addressing aspects such as cell isolation protocols and characteristics of these cells, as well as providing preliminary indications of the possibilities for use of these cells in future clinical applications.
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            Dose-dependent immunomodulatory effect of human stem cells from amniotic membrane: a comparison with human mesenchymal stem cells from adipose tissue.

            Bone marrow-derived mesenchymal stem cells (BMSCs) have been used for allogeneic application in tissue engineering but have certain drawbacks. Therefore, stem cells (SC)s derived from other adult tissue sources have been considered as an alternative. However, there is only limited knowledge on their immunomodulatory properties. The aim of our study was to compare the immunomodulatory potential of human amniotic mesenchymal and human amniotic epithelial cells with that of human adipose-derived SCs under identical experimental conditions. We have demonstrated a dose-dependent inhibition of peripheral blood mononuclear cell (PBMC) immune responses in mixed lymphocyte reactions (up to 66-93% inhibition) and phytohemagglutinin activation assays (up to 67-96% inhibition). The lowest SC-to-PBMC ratio able to inhibit PBMC proliferation significantly was 1:8. Subcultivation (passage 2-6) did not alter immunoinhibitory properties, whereas cryopreservation significantly reduced the immunomodulatory potential. Using transwell systems, we have demonstrated an inhibition mechanism that is dependent on cell contact. Additionally, in coculture with allogeneic PBMCs, SCs were well tolerated and at most provoked mild alloreactions in singular cases. This study demonstrates, for the first time, contact- and dose-dependent immunosuppression of mesenchymal and epithelial amniotic SC populations, as well as of adipose tissue-derived SCs. All three cell types may be considered as possible alternatives to BMSCs for allogeneic application in tissue engineering.
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              Sutureless repair of corneal injuries using naturally derived bioadhesive hydrogels

              We engineered a photocrosslinkable and transparent bioadhesive hydrogel for quick sealing, and repair of corneal defects.
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                Author and article information

                Contributors
                Journal
                Front Bioeng Biotechnol
                Front Bioeng Biotechnol
                Front. Bioeng. Biotechnol.
                Frontiers in Bioengineering and Biotechnology
                Frontiers Media S.A.
                2296-4185
                10 June 2021
                2021
                : 9
                : 685128
                Affiliations
                [1] 1Service de Chirurgie Maxillo-Faciale, Stomatologie et Odontologie Hospitalière, CHU Besançon , Besançon, France
                [2] 2Université Bourgogne Franche-Comté, INSERM, EFS BFC, UMR 1098, RIGHT Interactions Greffon-Hôte-Tumeur/Ingénierie Cellulaire et Génique , Besançon, France
                [3] 3Laboratoire de Nanomédecine, Imagerie, Thérapeutique EA 4662, Université Bourgogne Franche-Comté , Besançon, France
                [4] 4Regeneration, Molecular Oncology and TGFβ, IMIB-Arrixaca , Murcia, Spain
                [5] 5Deutsche Gesellschaft für Gewebetransplantation (DGFG) , Hannover, Germany
                [6] 6Pôle Médecine Bucco-dentaire, Hôpital Maison Blanche, CHU Reims , Reims, France
                [7] 7Université de Reims Champagne Ardenne, Biomatériaux et Inflammation en Site Osseux, Pôle Santé, URCA, BIOS EA 4691, UFR d’Odontologie , Reims, France
                [8] 8Université de Reims Champagne Ardenne, Biomatériaux et Inflammation en Site Osseux, Pôle Santé, URCA, HERVI EA3801, UFR de Médecine , Reims, France
                [9] 9Chirurgie Maxillo-Faciale – Stomatologie – Chirurgie Plastique Réparatrice et Esthétique - Chirurgie de la main, CHU de Dijon , Dijon, France
                [10] 10Université Bourgogne Franche-Comté , Besançon, France
                [11] 11Univ. Bordeaux, INSERM, BIOTIS, U1026 , Bordeaux, France
                [12] 12CHU Bordeaux, Service de chirurgie orale , Bordeaux, France
                [13] 13Établissement Français du Sang Nouvelle-Aquitaine, Bordeaux, France/INSERM U1035, Université de Bordeaux, Biothérapie des Maladies Génétiques Inflammatoires et Cancers (BMGIC) , Bordeaux, France
                [14] 14Établissement Français du Sang Bourgogne Franche-Comté , Besançon, France
                [15] 15CNRS, INSERM, UMR-9020-UMR-S 1277 Canther, Banque de Tissus CHU Lille , Lille, France
                [16] 16Service d’ophtalmologie, CHU Besançon , Besançon, France
                [17] 17Service de Chirurgie Orthopédique, Traumatologique et Plastique, CHU Besançon , Besançon, France
                Author notes

                Edited by: Peter Ponsaerts, University of Antwerp, Belgium

                Reviewed by: Yong-Can Huang, Peking University Shenzhen Hospital, China; Sebastian San Martin, Universidad de Valparaiso, Chile

                *Correspondence: Florelle Gindraux, fgindraux@ 123456chu-besancon.fr

                These authors share last authorship

                This article was submitted to Tissue Engineering and Regenerative Medicine, a section of the journal Frontiers in Bioengineering and Biotechnology

                Article
                10.3389/fbioe.2021.685128
                8222622
                34178969
                cab00d9c-c4c6-4859-aca7-4e0c0216d8c6
                Copyright © 2021 Odet, Louvrier, Meyer, Nicolas, Hofman, Chatelain, Mauprivez, Laurence, Kerdjoudj, Zwetyenga, Fricain, Lafarge, Pouthier, Marchetti, Gauthier, Fenelon and Gindraux.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 24 March 2021
                : 06 May 2021
                Page count
                Figures: 0, Tables: 3, Equations: 0, References: 108, Pages: 16, Words: 0
                Categories
                Bioengineering and Biotechnology
                Review

                amniotic membrane,oral and maxillo-facial surgery,oral mucosa,ophthalmology,wound healing

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