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Acute and chronic local inflammatory reaction after implantation of different extracellular porcine dermis collagen matrices in rats.

Abstract
Two cross-linked acellular porcine dermal collagen matrices (Permacol and NRX) were implanted into rats and the acute and chronic local inflammatory tissue reactions were investigated after 7, 14, 28, and 112 days. Both membranes were stable in vivo for up to 112 days. All investigated immune cell populations (CD68+ macrophages, CD163+ macrophages, T lymphocytes, MHC class II positive cells, mast cells, and NK cells) were present. Their amount decreased significantly over time compared to day 7 after implantation. A change from an acute to a chronic inflammation and an associated shift from proinflammatory M1-like to anti-inflammatory M2-like macrophages were observed. In the early phase there was a significant correlation of T cells to CD68+ (M1-like) macrophages, whereas in the chronic phase T lymphocytes were positively correlated with CD163+ (M2-like) macrophages. The material NRX showed an enhanced inflammatory reaction in comparison to Permacol possibly caused by material characteristics such as a twofold higher thickness of the membrane, roughness, and water absorption capacity. Nevertheless, a more pronounced regenerative process as, for example, indicated by nestin expression demonstrated its possible suitability for applications as wound repair material.
AuthorsSilke Lucke, Andreas Hoene, Uwe Walschus, Anette Kob, Jens-Wolfgang Pissarek, Michael Schlosser
JournalBioMed research international (Biomed Res Int) Vol. 2015 Pg. 938059 ( 2015) ISSN: 2314-6141 [Electronic] United States
PMID25648958 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Biocompatible Materials
  • Permacol
  • Collagen
Topics
  • Acellular Dermis (adverse effects)
  • Animals
  • Biocompatible Materials (adverse effects)
  • Chronic Disease
  • Collagen (adverse effects)
  • Inflammation (immunology)
  • Macrophages (immunology)
  • Prostheses and Implants
  • Rats
  • Swine
  • T-Lymphocytes (immunology)

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