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Original Paper

Clinical Application of a Tissue-Cultured Skin Autograft: An Alternative for the Treatment of Non-Healing or Slowly Healing Wounds?

Zöller N.a · Valesky E.a · Butting M.a · Hofmann M.a · Kippenberger S.a · Bereiter-Hahn J.b · Bernd A.a · Kaufmann R.a

Author affiliations

aDepartment of Dermatology, Venereology and Allergology, Goethe University Medical School, and bKinematic Cell Research Group, Goethe University, Frankfurt/Main, Germany

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Dermatology 2014;229:190-198

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Article / Publication Details

First-Page Preview
Abstract of Original Paper

Received: January 03, 2014
Accepted: April 17, 2014
Published online: September 06, 2014
Issue release date: November 2014

Number of Print Pages: 9
Number of Figures: 5
Number of Tables: 0

ISSN: 1018-8665 (Print)
eISSN: 1421-9832 (Online)

For additional information: https://www.karger.com/DRM

Abstract

Background: The treatment regime of non-healing or slowly healing wounds is constantly improving. One aspect is surgical defect coverage whereby mesh grafts and keratinocyte suspension are applied. Objective: Tissue-cultured skin autografts may be an alternative for the treatment of full-thickness wounds and wounds that cover large areas of the body surface. Methods: Autologous epidermal and dermal cells were isolated, expanded in vitro and seeded on collagen-elastin scaffolds. The developed autograft was immunohistochemically characterized and subsequently transplanted onto a facial chronic ulceration of a 71-year-old patient with vulnerable atrophic skin. Results: Characterization of the skin equivalent revealed comparability to healthy human skin due to the epidermal strata, differentiation and proliferation markers. Within 138 days, the skin structure at the transplantation site closely correlated with the adjacent undisturbed skin. Conclusion: The present study demonstrates the comparability of the developed organotypic skin equivalent to healthy human skin and the versatility for clinical applications.

© 2014 S. Karger AG, Basel


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Article / Publication Details

First-Page Preview
Abstract of Original Paper

Received: January 03, 2014
Accepted: April 17, 2014
Published online: September 06, 2014
Issue release date: November 2014

Number of Print Pages: 9
Number of Figures: 5
Number of Tables: 0

ISSN: 1018-8665 (Print)
eISSN: 1421-9832 (Online)

For additional information: https://www.karger.com/DRM


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