Polypropylene surgical mesh coated with extracellular matrix mitigates the host foreign body response.
Identifieur interne : 001C17 ( PubMed/Checkpoint ); précédent : 001C16; suivant : 001C18Polypropylene surgical mesh coated with extracellular matrix mitigates the host foreign body response.
Auteurs : Matthew T. Wolf [États-Unis] ; Christopher A. Carruthers ; Christopher L. Dearth ; Peter M. Crapo ; Alexander Huber ; Olivia A. Burnsed ; Ricardo Londono ; Scott A. Johnson ; Kerry A. Daly ; Elizabeth C. Stahl ; John M. Freund ; Christopher J. Medberry ; Lisa E. Carey ; Alejandro Nieponice ; Nicholas J. Amoroso ; Stephen F. BadylakSource :
- Journal of biomedical materials research. Part A [ 1552-4965 ] ; 2014.
Descripteurs français
- KwdFr :
- MESH :
- anatomopathologie : Réaction à corps étranger.
- métabolisme : Réaction à corps étranger.
- Animaux, Femelle, Filet chirurgical, Matrice extracellulaire, Matériaux revêtus, biocompatibles, Polypropylènes, Rat Sprague-Dawley, Rats, Test de matériaux.
English descriptors
- KwdEn :
- MESH :
- chemical , chemistry : Coated Materials, Biocompatible, Polypropylenes.
- chemistry : Extracellular Matrix.
- metabolism : Foreign-Body Reaction.
- pathology : Foreign-Body Reaction.
- Animals, Female, Materials Testing, Rats, Rats, Sprague-Dawley, Surgical Mesh.
Abstract
Surgical mesh devices composed of synthetic materials are commonly used for ventral hernia repair. These materials provide robust mechanical strength and are quickly incorporated into host tissue; factors that contribute to reduced hernia recurrence rates. However, such mesh devices cause a foreign body response with the associated complications of fibrosis and patient discomfort. In contrast, surgical mesh devices composed of naturally occurring extracellular matrix (ECM) are associated with constructive tissue remodeling, but lack the mechanical strength of synthetic materials. A method for applying a porcine dermal ECM hydrogel coating to a polypropylene mesh is described herein with the associated effects upon the host tissue response and biaxial mechanical behavior. Uncoated and ECM coated heavy-weight BARD™ Mesh were compared to the light-weight ULTRAPRO™ and BARD™ Soft Mesh devices in a rat partial thickness abdominal defect overlay model. The ECM coated mesh attenuated the pro-inflammatory response compared to all other devices, with a reduced cell accumulation and fewer foreign body giant cells. The ECM coating degraded by 35 days, and was replaced with loose connective tissue compared to the dense collagenous tissue associated with the uncoated polypropylene mesh device. Biaxial mechanical characterization showed that all of the mesh devices were of similar isotropic stiffness. Upon explanation, the light-weight mesh devices were more compliant than the coated or uncoated heavy-weight devices. This study shows that an ECM coating alters the default host response to a polypropylene mesh, but not the mechanical properties in an acute in vivo abdominal repair model.
DOI: 10.1002/jbm.a.34671
PubMed: 23873846
Affiliations:
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Part A</title><idno type="eISSN">1552-4965</idno><imprint><date when="2014" type="published">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals</term><term>Coated Materials, Biocompatible (chemistry)</term><term>Extracellular Matrix (chemistry)</term><term>Female</term><term>Foreign-Body Reaction (metabolism)</term><term>Foreign-Body Reaction (pathology)</term><term>Materials Testing</term><term>Polypropylenes (chemistry)</term><term>Rats</term><term>Rats, Sprague-Dawley</term><term>Surgical Mesh</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Animaux</term><term>Femelle</term><term>Filet chirurgical</term><term>Matrice extracellulaire ()</term><term>Matériaux revêtus, biocompatibles ()</term><term>Polypropylènes ()</term><term>Rat Sprague-Dawley</term><term>Rats</term><term>Réaction à corps étranger (anatomopathologie)</term><term>Réaction à corps étranger (métabolisme)</term><term>Test de matériaux</term></keywords><keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Coated Materials, Biocompatible</term><term>Polypropylenes</term></keywords><keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Réaction à corps étranger</term></keywords><keywords scheme="MESH" qualifier="chemistry" xml:lang="en"><term>Extracellular Matrix</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Foreign-Body Reaction</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Réaction à corps étranger</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Foreign-Body Reaction</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Female</term><term>Materials Testing</term><term>Rats</term><term>Rats, Sprague-Dawley</term><term>Surgical Mesh</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Animaux</term><term>Femelle</term><term>Filet chirurgical</term><term>Matrice extracellulaire</term><term>Matériaux revêtus, biocompatibles</term><term>Polypropylènes</term><term>Rat Sprague-Dawley</term><term>Rats</term><term>Test de matériaux</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Surgical mesh devices composed of synthetic materials are commonly used for ventral hernia repair. These materials provide robust mechanical strength and are quickly incorporated into host tissue; factors that contribute to reduced hernia recurrence rates. However, such mesh devices cause a foreign body response with the associated complications of fibrosis and patient discomfort. In contrast, surgical mesh devices composed of naturally occurring extracellular matrix (ECM) are associated with constructive tissue remodeling, but lack the mechanical strength of synthetic materials. A method for applying a porcine dermal ECM hydrogel coating to a polypropylene mesh is described herein with the associated effects upon the host tissue response and biaxial mechanical behavior. Uncoated and ECM coated heavy-weight BARD™ Mesh were compared to the light-weight ULTRAPRO™ and BARD™ Soft Mesh devices in a rat partial thickness abdominal defect overlay model. The ECM coated mesh attenuated the pro-inflammatory response compared to all other devices, with a reduced cell accumulation and fewer foreign body giant cells. The ECM coating degraded by 35 days, and was replaced with loose connective tissue compared to the dense collagenous tissue associated with the uncoated polypropylene mesh device. Biaxial mechanical characterization showed that all of the mesh devices were of similar isotropic stiffness. Upon explanation, the light-weight mesh devices were more compliant than the coated or uncoated heavy-weight devices. This study shows that an ECM coating alters the default host response to a polypropylene mesh, but not the mechanical properties in an acute in vivo abdominal repair model.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">23873846</PMID><DateCreated><Year>2015</Year><Month>05</Month><Day>01</Day></DateCreated><DateCompleted><Year>2016</Year><Month>01</Month><Day>08</Day></DateCompleted><DateRevised><Year>2016</Year><Month>10</Month><Day>19</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1552-4965</ISSN><JournalIssue CitedMedium="Internet"><Volume>102</Volume><Issue>1</Issue><PubDate><Year>2014</Year><Month>Jan</Month></PubDate></JournalIssue><Title>Journal of biomedical materials research. Part A</Title><ISOAbbreviation>J Biomed Mater Res A</ISOAbbreviation></Journal><ArticleTitle>Polypropylene surgical mesh coated with extracellular matrix mitigates the host foreign body response.</ArticleTitle><Pagination><MedlinePgn>234-46</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1002/jbm.a.34671</ELocationID><Abstract><AbstractText>Surgical mesh devices composed of synthetic materials are commonly used for ventral hernia repair. These materials provide robust mechanical strength and are quickly incorporated into host tissue; factors that contribute to reduced hernia recurrence rates. However, such mesh devices cause a foreign body response with the associated complications of fibrosis and patient discomfort. In contrast, surgical mesh devices composed of naturally occurring extracellular matrix (ECM) are associated with constructive tissue remodeling, but lack the mechanical strength of synthetic materials. A method for applying a porcine dermal ECM hydrogel coating to a polypropylene mesh is described herein with the associated effects upon the host tissue response and biaxial mechanical behavior. Uncoated and ECM coated heavy-weight BARD™ Mesh were compared to the light-weight ULTRAPRO™ and BARD™ Soft Mesh devices in a rat partial thickness abdominal defect overlay model. The ECM coated mesh attenuated the pro-inflammatory response compared to all other devices, with a reduced cell accumulation and fewer foreign body giant cells. The ECM coating degraded by 35 days, and was replaced with loose connective tissue compared to the dense collagenous tissue associated with the uncoated polypropylene mesh device. Biaxial mechanical characterization showed that all of the mesh devices were of similar isotropic stiffness. Upon explanation, the light-weight mesh devices were more compliant than the coated or uncoated heavy-weight devices. This study shows that an ECM coating alters the default host response to a polypropylene mesh, but not the mechanical properties in an acute in vivo abdominal repair model.</AbstractText><CopyrightInformation>Copyright © 2013 Wiley Periodicals, Inc., a Wiley Company.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Wolf</LastName><ForeName>Matthew T</ForeName><Initials>MT</Initials><AffiliationInfo><Affiliation>Department of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania; McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Carruthers</LastName><ForeName>Christopher A</ForeName><Initials>CA</Initials></Author><Author ValidYN="Y"><LastName>Dearth</LastName><ForeName>Christopher L</ForeName><Initials>CL</Initials></Author><Author ValidYN="Y"><LastName>Crapo</LastName><ForeName>Peter M</ForeName><Initials>PM</Initials></Author><Author ValidYN="Y"><LastName>Huber</LastName><ForeName>Alexander</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Burnsed</LastName><ForeName>Olivia A</ForeName><Initials>OA</Initials></Author><Author ValidYN="Y"><LastName>Londono</LastName><ForeName>Ricardo</ForeName><Initials>R</Initials></Author><Author ValidYN="Y"><LastName>Johnson</LastName><ForeName>Scott A</ForeName><Initials>SA</Initials></Author><Author ValidYN="Y"><LastName>Daly</LastName><ForeName>Kerry A</ForeName><Initials>KA</Initials></Author><Author ValidYN="Y"><LastName>Stahl</LastName><ForeName>Elizabeth C</ForeName><Initials>EC</Initials></Author><Author ValidYN="Y"><LastName>Freund</LastName><ForeName>John M</ForeName><Initials>JM</Initials></Author><Author ValidYN="Y"><LastName>Medberry</LastName><ForeName>Christopher J</ForeName><Initials>CJ</Initials></Author><Author ValidYN="Y"><LastName>Carey</LastName><ForeName>Lisa E</ForeName><Initials>LE</Initials></Author><Author ValidYN="Y"><LastName>Nieponice</LastName><ForeName>Alejandro</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Amoroso</LastName><ForeName>Nicholas J</ForeName><Initials>NJ</Initials></Author><Author ValidYN="Y"><LastName>Badylak</LastName><ForeName>Stephen F</ForeName><Initials>SF</Initials></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><GrantID>T32-EB001026</GrantID><Acronym>EB</Acronym><Agency>NIBIB NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>T32-HL76124-6</GrantID><Acronym>HL</Acronym><Agency>NHLBI NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>T32 EB001026</GrantID><Acronym>EB</Acronym><Agency>NIBIB NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>T32 HL076124</GrantID><Acronym>HL</Acronym><Agency>NHLBI NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>T32 EB003392</GrantID><Acronym>EB</Acronym><Agency>NIBIB NIH HHS</Agency><Country>United States</Country></Grant></GrantList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D052061">Research Support, N.I.H., Extramural</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType><PublicationType UI="D013486">Research Support, U.S. Gov't, Non-P.H.S.</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2013</Year><Month>07</Month><Day>19</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>J Biomed Mater Res A</MedlineTA><NlmUniqueID>101234237</NlmUniqueID><ISSNLinking>1549-3296</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D020099">Coated Materials, Biocompatible</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance 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MajorTopicYN="Y">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005109" MajorTopicYN="N">Extracellular Matrix</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005549" MajorTopicYN="N">Foreign-Body Reaction</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName><QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008422" MajorTopicYN="Y">Materials Testing</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D011126" MajorTopicYN="N">Polypropylenes</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D051381" MajorTopicYN="N">Rats</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D017207" MajorTopicYN="N">Rats, Sprague-Dawley</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D013526" MajorTopicYN="N">Surgical Mesh</DescriptorName></MeshHeading></MeshHeadingList><OtherID Source="NLM">NIHMS472873</OtherID><OtherID Source="NLM">PMC3808505</OtherID><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">coated surgical mesh</Keyword><Keyword MajorTopicYN="N">extracellular matrix</Keyword><Keyword MajorTopicYN="N">foreign body response</Keyword><Keyword MajorTopicYN="N">polypropylene</Keyword><Keyword MajorTopicYN="N">surgical mesh</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2012</Year><Month>09</Month><Day>18</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2013</Year><Month>02</Month><Day>15</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2013</Year><Month>02</Month><Day>19</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2013</Year><Month>7</Month><Day>23</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2013</Year><Month>7</Month><Day>23</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2016</Year><Month>1</Month><Day>9</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">23873846</ArticleId><ArticleId IdType="doi">10.1002/jbm.a.34671</ArticleId><ArticleId IdType="pmc">PMC3808505</ArticleId><ArticleId IdType="mid">NIHMS472873</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>États-Unis</li></country><region><li>Pennsylvanie</li></region></list><tree><noCountry><name sortKey="Amoroso, Nicholas J" sort="Amoroso, Nicholas J" uniqKey="Amoroso N" first="Nicholas J" last="Amoroso">Nicholas J. Amoroso</name><name sortKey="Badylak, Stephen F" sort="Badylak, Stephen F" uniqKey="Badylak S" first="Stephen F" last="Badylak">Stephen F. Badylak</name><name sortKey="Burnsed, Olivia A" sort="Burnsed, Olivia A" uniqKey="Burnsed O" first="Olivia A" last="Burnsed">Olivia A. Burnsed</name><name sortKey="Carey, Lisa E" sort="Carey, Lisa E" uniqKey="Carey L" first="Lisa E" last="Carey">Lisa E. Carey</name><name sortKey="Carruthers, Christopher A" sort="Carruthers, Christopher A" uniqKey="Carruthers C" first="Christopher A" last="Carruthers">Christopher A. Carruthers</name><name sortKey="Crapo, Peter M" sort="Crapo, Peter M" uniqKey="Crapo P" first="Peter M" last="Crapo">Peter M. Crapo</name><name sortKey="Daly, Kerry A" sort="Daly, Kerry A" uniqKey="Daly K" first="Kerry A" last="Daly">Kerry A. Daly</name><name sortKey="Dearth, Christopher L" sort="Dearth, Christopher L" uniqKey="Dearth C" first="Christopher L" last="Dearth">Christopher L. Dearth</name><name sortKey="Freund, John M" sort="Freund, John M" uniqKey="Freund J" first="John M" last="Freund">John M. Freund</name><name sortKey="Huber, Alexander" sort="Huber, Alexander" uniqKey="Huber A" first="Alexander" last="Huber">Alexander Huber</name><name sortKey="Johnson, Scott A" sort="Johnson, Scott A" uniqKey="Johnson S" first="Scott A" last="Johnson">Scott A. Johnson</name><name sortKey="Londono, Ricardo" sort="Londono, Ricardo" uniqKey="Londono R" first="Ricardo" last="Londono">Ricardo Londono</name><name sortKey="Medberry, Christopher J" sort="Medberry, Christopher J" uniqKey="Medberry C" first="Christopher J" last="Medberry">Christopher J. Medberry</name><name sortKey="Nieponice, Alejandro" sort="Nieponice, Alejandro" uniqKey="Nieponice A" first="Alejandro" last="Nieponice">Alejandro Nieponice</name><name sortKey="Stahl, Elizabeth C" sort="Stahl, Elizabeth C" uniqKey="Stahl E" first="Elizabeth C" last="Stahl">Elizabeth C. Stahl</name></noCountry><country name="États-Unis"><region name="Pennsylvanie"><name sortKey="Wolf, Matthew T" sort="Wolf, Matthew T" uniqKey="Wolf M" first="Matthew T" last="Wolf">Matthew T. Wolf</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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