Use of Amniotic Membrane and Its Derived Products for Bone Regeneration: A Systematic Review.

amniotic epithelial cells amniotic membrane amniotic mesenchymal stromal cells bone bone tissue engineering natural scaffold regenerative medicine

Journal

Frontiers in bioengineering and biotechnology
ISSN: 2296-4185
Titre abrégé: Front Bioeng Biotechnol
Pays: Switzerland
ID NLM: 101632513

Informations de publication

Date de publication:
2021
Historique:
received: 30 01 2021
accepted: 13 04 2021
entrez: 28 5 2021
pubmed: 29 5 2021
medline: 29 5 2021
Statut: epublish

Résumé

Thanks to their biological properties, amniotic membrane (AM), and its derivatives are considered as an attractive reservoir of stem cells and biological scaffolds for bone regenerative medicine. The objective of this systematic review was to assess the benefit of using AM and amniotic membrane-derived products for bone regeneration. An electronic search of the MEDLINE-Pubmed database and the Scopus database was carried out and the selection of articles was performed following PRISMA guidelines. This systematic review included 42 articles taking into consideration the studies in which AM, amniotic-derived epithelial cells (AECs), and amniotic mesenchymal stromal cells (AMSCs) show promising results for bone regeneration in animal models. Moreover, this review also presents some commercialized products derived from AM and discusses their application modalities. Finally, AM therapeutic benefit is highlighted in the reported clinical studies. This study is the first one to systematically review the therapeutic benefits of AM and amniotic membrane-derived products for bone defect healing. The AM is a promising alternative to the commercially available membranes used for guided bone regeneration. Additionally, AECs and AMSCs associated with an appropriate scaffold may also be ideal candidates for tissue engineering strategies applied to bone healing. Here, we summarized these findings and highlighted the relevance of these different products for bone regeneration.

Identifiants

pubmed: 34046400
doi: 10.3389/fbioe.2021.661332
pmc: PMC8144457
doi:

Types de publication

Systematic Review

Langues

eng

Pagination

661332

Informations de copyright

Copyright © 2021 Etchebarne, Fricain, Kerdjoudj, Di Pietro, Wolbank, Gindraux and Fenelon.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Marion Etchebarne (M)

Univ. Bordeaux, INSERM, BIOTIS, U1026, Bordeaux, France.
CHU Bordeaux, Department of Maxillofacial Surgery, Bordeaux, France.

Jean-Christophe Fricain (JC)

Univ. Bordeaux, INSERM, BIOTIS, U1026, Bordeaux, France.
CHU Bordeaux, Service de Chirurgie Orale, Bordeaux, France.

Halima Kerdjoudj (H)

Université de Reims Champagne Ardenne, EA 4691, Biomatériaux et Inflammation en Site Osseux (BIOS), Reims, France.
Université de Reims Champagne Ardenne, UFR d'Odontologie, Reims, France.

Roberta Di Pietro (R)

Department of Medicine and Ageing Sciences, Gabriele D'Annunzio University of Chieti-Pescara, Chieti, Italy.
StemTeCh Group, Gabriele D'Annunzio Foundation, Gabriele D'Annunzio University of Chieti-Pescara, Chieti, Italy.

Susanne Wolbank (S)

Ludwig Boltzmann Institute for Experimental and Clinical Traumatology, AUVA Research Center, Vienna, Austria.
Austrian Cluster for Tissue Regeneration, Vienna, Austria.

Florelle Gindraux (F)

Service de Chirurgie Orthopédique, Traumatologique et Plastique, CHU Besançon, Besançon, France.
Laboratoire de Nanomédecine, Imagerie, Thérapeutique EA 4662, Université Bourgogne Franche-Comté, Besançon, France.

Mathilde Fenelon (M)

Univ. Bordeaux, INSERM, BIOTIS, U1026, Bordeaux, France.
CHU Bordeaux, Service de Chirurgie Orale, Bordeaux, France.

Classifications MeSH