Host Response to Implanted Porcine-Derived Biologic Materials in a Primate Model of Abdominal Wall Repair
Three commercially available porcine-derived biologic meshes were implanted in an Old World primate abdominal wall resection repair model to compare biological outcome as a predictor of clinical efficacy. Tissues were explanted over a 6-month period and evaluated for gross pathology, wound healing s...
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Veröffentlicht in: | Tissue engineering. Part A 2008-12, Vol.14 (12), p.221-2031 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Three commercially available porcine-derived biologic meshes were implanted in an Old World primate abdominal wall resection repair model to compare biological outcome as a predictor of clinical efficacy. Tissues were explanted over a 6-month period and evaluated for gross pathology, wound healing strength, mesenchymal cellular repopulation, vascularity, and immune response.
In vivo
functional outcomes were correlated with
in vitro
profile for each material. Small intestinal submucosa-based implants demonstrated scar tissue formation and contraction, coincident with mesh pleating, and were characterized by immediate and significant cellular and humoral inflammatory responses. Porcine dermal-based grafts demonstrated significant graft pleating, minimal integration, and an absence of cellular repopulation and vascularization. However, a significant cellular immune response surrounded the grafts, coincident with poor initial wound healing strengths.
In vivo
observations for the three porcine-derived mesh products correlated with individual
in vitro
profiles, indicating an absence of characteristic biochemical markers and structural integrity. This correlation suggests that
in vivo
results observed for these mesh products are a direct consequence of specific manufacturing processes that yield modified collagen matrices. The resulting loss of biological and structural integrity elicits a foreign body response while hindering normal healing and tissue integration. |
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ISSN: | 1937-3341 1937-335X |
DOI: | 10.1089/ten.tea.2007.0317 |