Milk fat globule epidermal growth factor 8 inhibits periodontitis in non‐human primates and its gingival crevicular fluid levels can differentiate periodontal health from disease in humans
Aim We have previously shown that the secreted glycoprotein milk fat globule epidermal growth factor 8 (MFG‐E8) has anti‐inflammatory and anti‐osteoclastogenic properties. Our objective was to investigate the potential of MFG‐E8 as a diagnostic or therapeutic agent in periodontitis. Materials and Me...
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Veröffentlicht in: | Journal of clinical periodontology 2017-05, Vol.44 (5), p.472-483 |
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creator | Kajikawa, Tetsuhiro Meshikhes, Fatimah Maekawa, Tomoki Hajishengallis, Evlambia Hosur, Kavita B. Abe, Toshiharu Moss, Kevin Chavakis, Triantafyllos Hajishengallis, George |
description | Aim
We have previously shown that the secreted glycoprotein milk fat globule epidermal growth factor 8 (MFG‐E8) has anti‐inflammatory and anti‐osteoclastogenic properties. Our objective was to investigate the potential of MFG‐E8 as a diagnostic or therapeutic agent in periodontitis.
Materials and Methods
Periodontitis was induced in non‐human primates (NHPs) by placing ligatures around posterior teeth on both halves of the mandible for a split‐mouth design: one side was treated with MFG‐E8‐Fc and the other with Fc control. Disease was assessed by clinical periodontal examinations, radiographic analysis of bone loss, and analysis of cytokine mRNA expression in gingival biopsy samples. Gingival crevicular fluid (GCF) was collected from human healthy volunteers or subjects with gingivitis, chronic moderate periodontitis, or chronic severe periodontitis. Additionally, GCF was collected from a subset of severe periodontitis patients following scaling and root planing (SRP) and after pocket reduction surgery. GCF was analysed to quantify MFG‐E8 and periodontitis‐relevant cytokines using multiplex assays.
Results
In NHPs, sites treated with MFG‐E8‐Fc exhibited significantly less ligature‐induced periodontal inflammation and bone loss than Fc control‐treated sites. In humans, the GCF levels of MFG‐E8 were significantly higher in health than in periodontitis, whereas the reverse was true for the proinflammatory cytokines tested. Consistently, MFG‐E8 was elevated in GCF after both non‐surgical (SRP) and surgical periodontal treatment of periodontitis patients.
Conclusion
MFG‐E8 is, in principle, a novel therapeutic agent and biomarker of periodontitis. |
doi_str_mv | 10.1111/jcpe.12707 |
format | Article |
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We have previously shown that the secreted glycoprotein milk fat globule epidermal growth factor 8 (MFG‐E8) has anti‐inflammatory and anti‐osteoclastogenic properties. Our objective was to investigate the potential of MFG‐E8 as a diagnostic or therapeutic agent in periodontitis.
Materials and Methods
Periodontitis was induced in non‐human primates (NHPs) by placing ligatures around posterior teeth on both halves of the mandible for a split‐mouth design: one side was treated with MFG‐E8‐Fc and the other with Fc control. Disease was assessed by clinical periodontal examinations, radiographic analysis of bone loss, and analysis of cytokine mRNA expression in gingival biopsy samples. Gingival crevicular fluid (GCF) was collected from human healthy volunteers or subjects with gingivitis, chronic moderate periodontitis, or chronic severe periodontitis. Additionally, GCF was collected from a subset of severe periodontitis patients following scaling and root planing (SRP) and after pocket reduction surgery. GCF was analysed to quantify MFG‐E8 and periodontitis‐relevant cytokines using multiplex assays.
Results
In NHPs, sites treated with MFG‐E8‐Fc exhibited significantly less ligature‐induced periodontal inflammation and bone loss than Fc control‐treated sites. In humans, the GCF levels of MFG‐E8 were significantly higher in health than in periodontitis, whereas the reverse was true for the proinflammatory cytokines tested. Consistently, MFG‐E8 was elevated in GCF after both non‐surgical (SRP) and surgical periodontal treatment of periodontitis patients.
Conclusion
MFG‐E8 is, in principle, a novel therapeutic agent and biomarker of periodontitis.</description><identifier>ISSN: 0303-6979</identifier><identifier>EISSN: 1600-051X</identifier><identifier>DOI: 10.1111/jcpe.12707</identifier><identifier>PMID: 28207941</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Biomarkers ; Biopsy ; Bone loss ; Cytokines ; Dentistry ; Epidermal growth factor ; Gene expression ; Gingiva ; Gingivitis ; Glycoproteins ; Gum disease ; Inflammation ; Mandible ; Milk ; milk fat globule epidermal growth factor 8 ; Milk fat globule membranes ; non‐human primates ; Periodontitis ; Scaling ; Surgery ; Teeth</subject><ispartof>Journal of clinical periodontology, 2017-05, Vol.44 (5), p.472-483</ispartof><rights>2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><rights>2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><rights>Copyright © 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5007-17096710701da89c79a00c8d0263a1e2ab4ec10f1d92480f47d1727af08d3e313</citedby><cites>FETCH-LOGICAL-c5007-17096710701da89c79a00c8d0263a1e2ab4ec10f1d92480f47d1727af08d3e313</cites><orcidid>0000-0001-7392-8852 ; 0000-0003-4715-1538</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjcpe.12707$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjcpe.12707$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28207941$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kajikawa, Tetsuhiro</creatorcontrib><creatorcontrib>Meshikhes, Fatimah</creatorcontrib><creatorcontrib>Maekawa, Tomoki</creatorcontrib><creatorcontrib>Hajishengallis, Evlambia</creatorcontrib><creatorcontrib>Hosur, Kavita B.</creatorcontrib><creatorcontrib>Abe, Toshiharu</creatorcontrib><creatorcontrib>Moss, Kevin</creatorcontrib><creatorcontrib>Chavakis, Triantafyllos</creatorcontrib><creatorcontrib>Hajishengallis, George</creatorcontrib><title>Milk fat globule epidermal growth factor 8 inhibits periodontitis in non‐human primates and its gingival crevicular fluid levels can differentiate periodontal health from disease in humans</title><title>Journal of clinical periodontology</title><addtitle>J Clin Periodontol</addtitle><description>Aim
We have previously shown that the secreted glycoprotein milk fat globule epidermal growth factor 8 (MFG‐E8) has anti‐inflammatory and anti‐osteoclastogenic properties. Our objective was to investigate the potential of MFG‐E8 as a diagnostic or therapeutic agent in periodontitis.
Materials and Methods
Periodontitis was induced in non‐human primates (NHPs) by placing ligatures around posterior teeth on both halves of the mandible for a split‐mouth design: one side was treated with MFG‐E8‐Fc and the other with Fc control. Disease was assessed by clinical periodontal examinations, radiographic analysis of bone loss, and analysis of cytokine mRNA expression in gingival biopsy samples. Gingival crevicular fluid (GCF) was collected from human healthy volunteers or subjects with gingivitis, chronic moderate periodontitis, or chronic severe periodontitis. Additionally, GCF was collected from a subset of severe periodontitis patients following scaling and root planing (SRP) and after pocket reduction surgery. GCF was analysed to quantify MFG‐E8 and periodontitis‐relevant cytokines using multiplex assays.
Results
In NHPs, sites treated with MFG‐E8‐Fc exhibited significantly less ligature‐induced periodontal inflammation and bone loss than Fc control‐treated sites. In humans, the GCF levels of MFG‐E8 were significantly higher in health than in periodontitis, whereas the reverse was true for the proinflammatory cytokines tested. Consistently, MFG‐E8 was elevated in GCF after both non‐surgical (SRP) and surgical periodontal treatment of periodontitis patients.
Conclusion
MFG‐E8 is, in principle, a novel therapeutic agent and biomarker of periodontitis.</description><subject>Biomarkers</subject><subject>Biopsy</subject><subject>Bone loss</subject><subject>Cytokines</subject><subject>Dentistry</subject><subject>Epidermal growth factor</subject><subject>Gene expression</subject><subject>Gingiva</subject><subject>Gingivitis</subject><subject>Glycoproteins</subject><subject>Gum disease</subject><subject>Inflammation</subject><subject>Mandible</subject><subject>Milk</subject><subject>milk fat globule epidermal growth factor 8</subject><subject>Milk fat globule membranes</subject><subject>non‐human primates</subject><subject>Periodontitis</subject><subject>Scaling</subject><subject>Surgery</subject><subject>Teeth</subject><issn>0303-6979</issn><issn>1600-051X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9kcFu1DAURS0EokNhwwcgS2wqpJT3kkwcL9GoUFARLEBiF3nslxkPThzsZKru-gl8ER_Dl-DMFJBY4I0lv3PvffJl7CnCOabzcqcHOsdcgLjHFlgBZLDEL_fZAgooskoKecIexbgDQFEUxUN2ktc5CFnigv14b91X3qqRb5xfT444DdZQ6JTjm-Cvx20a6tEHXnPbb-3ajpEPFKw3vh_taGN65r3vf95-306d6vkQbKdGilz1hs_0xvYbu09-OtDe6smpwFs3WcMd7clFrpPK2LalQMkyaf8GJNWWlJu3CL5LVCQVaY48hMXH7EGrXKQnd_cp-_z64tPqMrv68Obt6tVVppcAIkMBshIIAtCoWmohFYCuDeRVoZBytS5JI7RoZF7W0JbCoMiFaqE2BRVYnLKzo-8Q_LeJ4th0NmpyTvXkp9hgXUlZyRzyhD7_B935KfRpu0TJWi4RRZmoF0dKBx9joLY5_Fu4aRCaudVmbrU5tJrgZ3eW07oj8wf9XWMC8AhcW0c3_7Fq3q0-XhxNfwE9D7FE</recordid><startdate>201705</startdate><enddate>201705</enddate><creator>Kajikawa, Tetsuhiro</creator><creator>Meshikhes, Fatimah</creator><creator>Maekawa, Tomoki</creator><creator>Hajishengallis, Evlambia</creator><creator>Hosur, Kavita B.</creator><creator>Abe, Toshiharu</creator><creator>Moss, Kevin</creator><creator>Chavakis, Triantafyllos</creator><creator>Hajishengallis, George</creator><general>Blackwell Publishing Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7392-8852</orcidid><orcidid>https://orcid.org/0000-0003-4715-1538</orcidid></search><sort><creationdate>201705</creationdate><title>Milk fat globule epidermal growth factor 8 inhibits periodontitis in non‐human primates and its gingival crevicular fluid levels can differentiate periodontal health from disease in humans</title><author>Kajikawa, Tetsuhiro ; Meshikhes, Fatimah ; Maekawa, Tomoki ; Hajishengallis, Evlambia ; Hosur, Kavita B. ; Abe, Toshiharu ; Moss, Kevin ; Chavakis, Triantafyllos ; Hajishengallis, George</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5007-17096710701da89c79a00c8d0263a1e2ab4ec10f1d92480f47d1727af08d3e313</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Biomarkers</topic><topic>Biopsy</topic><topic>Bone loss</topic><topic>Cytokines</topic><topic>Dentistry</topic><topic>Epidermal growth factor</topic><topic>Gene expression</topic><topic>Gingiva</topic><topic>Gingivitis</topic><topic>Glycoproteins</topic><topic>Gum disease</topic><topic>Inflammation</topic><topic>Mandible</topic><topic>Milk</topic><topic>milk fat globule epidermal growth factor 8</topic><topic>Milk fat globule membranes</topic><topic>non‐human primates</topic><topic>Periodontitis</topic><topic>Scaling</topic><topic>Surgery</topic><topic>Teeth</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kajikawa, Tetsuhiro</creatorcontrib><creatorcontrib>Meshikhes, Fatimah</creatorcontrib><creatorcontrib>Maekawa, Tomoki</creatorcontrib><creatorcontrib>Hajishengallis, Evlambia</creatorcontrib><creatorcontrib>Hosur, Kavita B.</creatorcontrib><creatorcontrib>Abe, Toshiharu</creatorcontrib><creatorcontrib>Moss, Kevin</creatorcontrib><creatorcontrib>Chavakis, Triantafyllos</creatorcontrib><creatorcontrib>Hajishengallis, George</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of clinical periodontology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kajikawa, Tetsuhiro</au><au>Meshikhes, Fatimah</au><au>Maekawa, Tomoki</au><au>Hajishengallis, Evlambia</au><au>Hosur, Kavita B.</au><au>Abe, Toshiharu</au><au>Moss, Kevin</au><au>Chavakis, Triantafyllos</au><au>Hajishengallis, George</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Milk fat globule epidermal growth factor 8 inhibits periodontitis in non‐human primates and its gingival crevicular fluid levels can differentiate periodontal health from disease in humans</atitle><jtitle>Journal of clinical periodontology</jtitle><addtitle>J Clin Periodontol</addtitle><date>2017-05</date><risdate>2017</risdate><volume>44</volume><issue>5</issue><spage>472</spage><epage>483</epage><pages>472-483</pages><issn>0303-6979</issn><eissn>1600-051X</eissn><abstract>Aim
We have previously shown that the secreted glycoprotein milk fat globule epidermal growth factor 8 (MFG‐E8) has anti‐inflammatory and anti‐osteoclastogenic properties. Our objective was to investigate the potential of MFG‐E8 as a diagnostic or therapeutic agent in periodontitis.
Materials and Methods
Periodontitis was induced in non‐human primates (NHPs) by placing ligatures around posterior teeth on both halves of the mandible for a split‐mouth design: one side was treated with MFG‐E8‐Fc and the other with Fc control. Disease was assessed by clinical periodontal examinations, radiographic analysis of bone loss, and analysis of cytokine mRNA expression in gingival biopsy samples. Gingival crevicular fluid (GCF) was collected from human healthy volunteers or subjects with gingivitis, chronic moderate periodontitis, or chronic severe periodontitis. Additionally, GCF was collected from a subset of severe periodontitis patients following scaling and root planing (SRP) and after pocket reduction surgery. GCF was analysed to quantify MFG‐E8 and periodontitis‐relevant cytokines using multiplex assays.
Results
In NHPs, sites treated with MFG‐E8‐Fc exhibited significantly less ligature‐induced periodontal inflammation and bone loss than Fc control‐treated sites. In humans, the GCF levels of MFG‐E8 were significantly higher in health than in periodontitis, whereas the reverse was true for the proinflammatory cytokines tested. Consistently, MFG‐E8 was elevated in GCF after both non‐surgical (SRP) and surgical periodontal treatment of periodontitis patients.
Conclusion
MFG‐E8 is, in principle, a novel therapeutic agent and biomarker of periodontitis.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>28207941</pmid><doi>10.1111/jcpe.12707</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-7392-8852</orcidid><orcidid>https://orcid.org/0000-0003-4715-1538</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biomarkers Biopsy Bone loss Cytokines Dentistry Epidermal growth factor Gene expression Gingiva Gingivitis Glycoproteins Gum disease Inflammation Mandible Milk milk fat globule epidermal growth factor 8 Milk fat globule membranes non‐human primates Periodontitis Scaling Surgery Teeth |
title | Milk fat globule epidermal growth factor 8 inhibits periodontitis in non‐human primates and its gingival crevicular fluid levels can differentiate periodontal health from disease in humans |
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