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Inflammatory Reaction as Determinant of Foreign Body Reaction Is an Early and Susceptible Event after Mesh Implantation
Purpose. To investigate and relate the ultrashort-term and long-term courses of determinants for foreign body reaction as biocompatibility predictors for meshes in an animal model. Materials and Methods. Three different meshes (TVT, UltraPro, and PVDF) were implanted in sheep. Native and plasma coat...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3982404/ https://www.ncbi.nlm.nih.gov/pubmed/24783209 http://dx.doi.org/10.1155/2014/510807 |
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author | Gerullis, Holger Georgas, Evangelos Borós, Mihaly Klosterhalfen, Bernd Eimer, Christoph Arndt, Christian Otto, Stephan Barski, Dimitri Ysebaert, Dirk Ramon, Albert Otto, Thomas |
author_facet | Gerullis, Holger Georgas, Evangelos Borós, Mihaly Klosterhalfen, Bernd Eimer, Christoph Arndt, Christian Otto, Stephan Barski, Dimitri Ysebaert, Dirk Ramon, Albert Otto, Thomas |
author_sort | Gerullis, Holger |
collection | PubMed |
description | Purpose. To investigate and relate the ultrashort-term and long-term courses of determinants for foreign body reaction as biocompatibility predictors for meshes in an animal model. Materials and Methods. Three different meshes (TVT, UltraPro, and PVDF) were implanted in sheep. Native and plasma coated meshes were placed bilaterally: (a) interaperitoneally, (b) as fascia onlay, and (c) as muscle onlay (fascia sublay). At 5 min, 20 min, 60 min, and 120 min meshes were explanted and histochemically investigated for inflammatory infiltrate, macrophage infiltration, vessel formation, myofibroblast invasion, and connective tissue accumulation. The results were related to long-term values over 24 months. Results. Macrophage invasion reached highest extents with up to 60% in short-term and decreased within 24 months to about 30%. Inflammatory infiltrate increased within the first 2 hours, the reached levels and the different extents and ranking among the investigated meshes remained stable during long-term follow up. For myofibroblasts, connective tissue, and CD31+ cells, no activity was detected during the first 120 min. Conclusion. The local inflammatory reaction is an early and susceptible event after mesh implantation. It cannot be influenced by prior plasma coating and does not depend on the localisation of implantation. |
format | Online Article Text |
id | pubmed-3982404 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-39824042014-04-29 Inflammatory Reaction as Determinant of Foreign Body Reaction Is an Early and Susceptible Event after Mesh Implantation Gerullis, Holger Georgas, Evangelos Borós, Mihaly Klosterhalfen, Bernd Eimer, Christoph Arndt, Christian Otto, Stephan Barski, Dimitri Ysebaert, Dirk Ramon, Albert Otto, Thomas Biomed Res Int Research Article Purpose. To investigate and relate the ultrashort-term and long-term courses of determinants for foreign body reaction as biocompatibility predictors for meshes in an animal model. Materials and Methods. Three different meshes (TVT, UltraPro, and PVDF) were implanted in sheep. Native and plasma coated meshes were placed bilaterally: (a) interaperitoneally, (b) as fascia onlay, and (c) as muscle onlay (fascia sublay). At 5 min, 20 min, 60 min, and 120 min meshes were explanted and histochemically investigated for inflammatory infiltrate, macrophage infiltration, vessel formation, myofibroblast invasion, and connective tissue accumulation. The results were related to long-term values over 24 months. Results. Macrophage invasion reached highest extents with up to 60% in short-term and decreased within 24 months to about 30%. Inflammatory infiltrate increased within the first 2 hours, the reached levels and the different extents and ranking among the investigated meshes remained stable during long-term follow up. For myofibroblasts, connective tissue, and CD31+ cells, no activity was detected during the first 120 min. Conclusion. The local inflammatory reaction is an early and susceptible event after mesh implantation. It cannot be influenced by prior plasma coating and does not depend on the localisation of implantation. Hindawi Publishing Corporation 2014 2014-03-26 /pmc/articles/PMC3982404/ /pubmed/24783209 http://dx.doi.org/10.1155/2014/510807 Text en Copyright © 2014 Holger Gerullis et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Gerullis, Holger Georgas, Evangelos Borós, Mihaly Klosterhalfen, Bernd Eimer, Christoph Arndt, Christian Otto, Stephan Barski, Dimitri Ysebaert, Dirk Ramon, Albert Otto, Thomas Inflammatory Reaction as Determinant of Foreign Body Reaction Is an Early and Susceptible Event after Mesh Implantation |
title | Inflammatory Reaction as Determinant of Foreign Body Reaction Is an Early and Susceptible Event after Mesh Implantation |
title_full | Inflammatory Reaction as Determinant of Foreign Body Reaction Is an Early and Susceptible Event after Mesh Implantation |
title_fullStr | Inflammatory Reaction as Determinant of Foreign Body Reaction Is an Early and Susceptible Event after Mesh Implantation |
title_full_unstemmed | Inflammatory Reaction as Determinant of Foreign Body Reaction Is an Early and Susceptible Event after Mesh Implantation |
title_short | Inflammatory Reaction as Determinant of Foreign Body Reaction Is an Early and Susceptible Event after Mesh Implantation |
title_sort | inflammatory reaction as determinant of foreign body reaction is an early and susceptible event after mesh implantation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3982404/ https://www.ncbi.nlm.nih.gov/pubmed/24783209 http://dx.doi.org/10.1155/2014/510807 |
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