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Allogenic adipose-derived stem cells in diabetic foot ulcer treatment: clinical effectiveness, safety, survival in the wound site, and proteomic impact.

Autor
Zieliński, Jakub
Lewandowska-Szumiel, Malgorzata
Czupryniak, Leszek
Paleska, Barbara
Noszczyk, Maria
Grzela, Tomasz
Sieńko, Damian
Mieczkowski, Mateusz
Konarzewska, Magdalena
Gasperowicz, Piotr
Data publikacji
2023
Abstrakt (EN)

Although encouraging results of adipose-derived stem cell (ADSC) use in wound healing are available, the mechanism of action has been studied mainly in vitro and in animals. This work aimed to examine the safety and efficacy of allogenic ADSCs in human diabetic foot ulcer treatment, in combination with the analyses of the wound. Equal groups of 23 participants each received fibrin gel with ADSCs or fibrin gel alone. The clinical effects were assessed at four time points: days 7, 14, 21 and 49. Material collected during debridement from a subset of each group was analyzed for the presence of ADSC donor DNA and proteomic changes. The reduction in wound size was greater at all subsequent visits, significantly on day 21 and 49, and the time to 50% reduction in the wound size was significantly shorter in patients who received ADSCs. Complete healing was achieved at the end of the study in seven patients treated with ADSCs vs. one treated without ADSCs. One week after ADSC application, 34 proteins significantly differentiated the material from both groups, seven of which, i.e., GAPDH, CAT, ACTN1, KRT1, KRT9, SCL4A1, and TPI, positively correlated with the healing rate. We detected ADSC donor DNA up to 21 days after administration. We confirmed ADSC-related improvement in wound healing that correlated with the molecular background, which provides insights into the role of ADSCs in wound healing—a step toward the development of cell-based therapies.

Słowa kluczowe EN
Cell therapy
Diabetic foot ulcer
Adipose-derived stem cells
Proteomics
Clinical trials
Allogenic cell therapy
Dyscyplina PBN
nauki medyczne
Czasopismo
International Journal of Molecular Sciences
Tom
24
Zeszyt
(2)
Strony od-do
1-16
ISSN
1422-0067
Data udostępnienia w otwartym dostępie
2023-01-12
Licencja otwartego dostępu
Uznanie autorstwa