Supportive use of platelet-rich plasma and stromal vascular fraction for cell-assisted fat transfer of skin radiation-induced lesions in nude mice.


Journal

Burns : journal of the International Society for Burn Injuries
ISSN: 1879-1409
Titre abrégé: Burns
Pays: Netherlands
ID NLM: 8913178

Informations de publication

Date de publication:
11 2020
Historique:
received: 28 08 2019
revised: 15 12 2019
accepted: 15 04 2020
pubmed: 2 6 2020
medline: 21 12 2021
entrez: 2 6 2020
Statut: ppublish

Résumé

External radiotherapy has become indispensable in oncological therapies. Unfortunately, radiation is responsible for serious side effects, such as radiodermatitis. The skin is weakened and ulcerated. Our study aimed to evaluate the subcutaneous transfer of microfat (MF) alone and two mixes: MF+Platelet-rich plasma (PRP) and MF+stromal vascular fraction (SVF) to treat radiation-induced skin lesions. We defined randomly five experimental groups of nine mice: 1 healthy control group and 4 irradiated (60 Grey) and treated groups. The skin lesions were treated 3 months after irradiation by MF, MF+PRP (50%-50%), MF+SVF (90%-10%) or Ringer-lactate subcutaneous injections. Wound healing was evaluated at 1, 2 and 3 months post-injection and histological wound analysis at 3 months, after euthanasia. All the irradiated mice presented with wounds. After sham-injection, the wound area increased by 91.1±71.1% versus a decrease of 15.9±23.1% after MF alone (NS), 27.3±23.8% after MF+SVF (NS) and 76.4±7.7% after MF+PRP (P=0.032). A significative reduction of skin thickness in wound periphery was measured for the three treated groups compared to sham-injection (P<0.05) but not in the healed wounds (NS). The most important subcutaneous neo-vessel density was shown after MF+SVF injection. The MF+PRP mix was the most efficient product to increase healing. The MF+SVF mix showed the highest rate of neo-angiogenesis but was disappointing in terms of healing. Not gradable.

Sections du résumé

BACKGROUND
External radiotherapy has become indispensable in oncological therapies. Unfortunately, radiation is responsible for serious side effects, such as radiodermatitis. The skin is weakened and ulcerated. Our study aimed to evaluate the subcutaneous transfer of microfat (MF) alone and two mixes: MF+Platelet-rich plasma (PRP) and MF+stromal vascular fraction (SVF) to treat radiation-induced skin lesions.
METHOD
We defined randomly five experimental groups of nine mice: 1 healthy control group and 4 irradiated (60 Grey) and treated groups. The skin lesions were treated 3 months after irradiation by MF, MF+PRP (50%-50%), MF+SVF (90%-10%) or Ringer-lactate subcutaneous injections. Wound healing was evaluated at 1, 2 and 3 months post-injection and histological wound analysis at 3 months, after euthanasia.
RESULTS
All the irradiated mice presented with wounds. After sham-injection, the wound area increased by 91.1±71.1% versus a decrease of 15.9±23.1% after MF alone (NS), 27.3±23.8% after MF+SVF (NS) and 76.4±7.7% after MF+PRP (P=0.032). A significative reduction of skin thickness in wound periphery was measured for the three treated groups compared to sham-injection (P<0.05) but not in the healed wounds (NS). The most important subcutaneous neo-vessel density was shown after MF+SVF injection.
CONCLUSION
The MF+PRP mix was the most efficient product to increase healing. The MF+SVF mix showed the highest rate of neo-angiogenesis but was disappointing in terms of healing.
LEVEL OF EVIDENCE
Not gradable.

Identifiants

pubmed: 32475796
pii: S0305-4179(20)30328-4
doi: 10.1016/j.burns.2020.04.020
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1641-1652

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2020 Elsevier Ltd and ISBI. All rights reserved.

Auteurs

Baptiste Bertrand (B)

Department of Plastic Surgery, La Conception Hospital, Assistance Publique - Hôpitaux de Marseille, France; Aix-Marseille Univ, C2VN, INSERM, INRA, France. Electronic address: Baptiste.bertrand@ap-hm.fr.

Julia Eraud (J)

Department of Plastic Surgery, La Conception Hospital, Assistance Publique - Hôpitaux de Marseille, France. Electronic address: Julia.eraud@ap-hm.fr.

Mélanie Velier (M)

Aix-Marseille Univ, C2VN, INSERM, INRA, France; Culture and Cell Therapy Laboratory, INSERM CICBT-1409, La Conception Hospital, Assistance Publique - Hôpitaux de Marseille, France. Electronic address: Melanie.velier@ap-hm.fr.

Cécile Cauvin (C)

Department of Radiotherapy, Hopital Privé Clairval, Marseille, France. Electronic address: Cecile.cauvin@yahoo.fr.

Nicolas Macagno (N)

Department of Pathology, la Timone Hospital, Assistance Publique - Hôpitaux de Marseille, France. Electronic address: Nicolas.macagno@ap-hm.fr.

Mohamed Boucekine (M)

Aix-Marseille Univ, EA 3279 - Public Health, Chronic Diseases and Quality of Life - Research Unit, France. Electronic address: boucekine.m@gmail.com.

Cécile Philandrianos (C)

Department of Plastic Surgery, La Conception Hospital, Assistance Publique - Hôpitaux de Marseille, France. Electronic address: Cecile.philandrianos@ap-hm.fr.

Dominique Casanova (D)

Department of Plastic Surgery, La Conception Hospital, Assistance Publique - Hôpitaux de Marseille, France. Electronic address: Dominique.casanova@ap-hm.fr.

Jeremy Magalon (J)

Aix-Marseille Univ, C2VN, INSERM, INRA, France; Culture and Cell Therapy Laboratory, INSERM CICBT-1409, La Conception Hospital, Assistance Publique - Hôpitaux de Marseille, France. Electronic address: Jeremy.magalon@ap-hm.fr.

Florence Sabatier (F)

Aix-Marseille Univ, C2VN, INSERM, INRA, France; Culture and Cell Therapy Laboratory, INSERM CICBT-1409, La Conception Hospital, Assistance Publique - Hôpitaux de Marseille, France. Electronic address: Florence.sabatier@ap-hm.fr.

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