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
Hauptverfasser: Kajikawa, Tetsuhiro, Meshikhes, Fatimah, Maekawa, Tomoki, Hajishengallis, Evlambia, Hosur, Kavita B., Abe, Toshiharu, Moss, Kevin, Chavakis, Triantafyllos, Hajishengallis, George
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container_end_page 483
container_issue 5
container_start_page 472
container_title Journal of clinical periodontology
container_volume 44
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
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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 &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd</rights><rights>2017 John Wiley &amp; Sons A/S. 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Published by John Wiley &amp; 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 &amp; Calcified Tissue Abstracts</collection><collection>ProQuest Health &amp; 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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