VWF protects FVIII from endocytosis by dendritic cells and subsequent presentation to immune effectors
Von Willebrand factor (VWF) is a chaperone molecule for procoagulant factor VIII (FVIII). Its role in the reduction of the immunogenicity of therapeutic FVIII in patients with hemophilia A has been evoked but lacks clear cellular and molecular rationale. Here, we demonstrate that VWF protects FVIII...
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Veröffentlicht in: | Blood 2007-01, Vol.109 (2), p.610-612 |
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creator | Dasgupta, Suryasarathi Repessé, Yohann Bayry, Jagadeesh Navarrete, Ana-Maria Wootla, Bharath Delignat, Sandrine Irinopoulou, Theano Kamaté, Caroline Saint-Remy, Jean-Marie Jacquemin, Marc Lenting, Peter J. Borel-Derlon, Annie Kaveri, Srinivas V. Lacroix-Desmazes, Sébastien |
description | Von Willebrand factor (VWF) is a chaperone molecule for procoagulant factor VIII (FVIII). Its role in the reduction of the immunogenicity of therapeutic FVIII in patients with hemophilia A has been evoked but lacks clear cellular and molecular rationale. Here, we demonstrate that VWF protects FVIII from being endocytosed by human dendritic cells (DCs) and subsequently presented to FVIII-specific T cells. The immunoprotective effect of VWF requires a physical interaction with FVIII because the endocytosis of FVIII was significantly restored on hindering the formation of the VWF-FVIII complex. Interestingly, VWF had no direct inhibitory effect either on the ability of DCs to present antigenic peptides or on the activation potency of CD4+ T cells. We thus propose that VWF may reduce the immunogenicity of FVIII by preventing, upstream from the activation of immune effectors, the entry of FVIII in professional antigen-presenting cells. |
doi_str_mv | 10.1182/blood-2006-05-022756 |
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Its role in the reduction of the immunogenicity of therapeutic FVIII in patients with hemophilia A has been evoked but lacks clear cellular and molecular rationale. Here, we demonstrate that VWF protects FVIII from being endocytosed by human dendritic cells (DCs) and subsequently presented to FVIII-specific T cells. The immunoprotective effect of VWF requires a physical interaction with FVIII because the endocytosis of FVIII was significantly restored on hindering the formation of the VWF-FVIII complex. Interestingly, VWF had no direct inhibitory effect either on the ability of DCs to present antigenic peptides or on the activation potency of CD4+ T cells. We thus propose that VWF may reduce the immunogenicity of FVIII by preventing, upstream from the activation of immune effectors, the entry of FVIII in professional antigen-presenting cells.</description><identifier>ISSN: 0006-4971</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood-2006-05-022756</identifier><identifier>PMID: 16985172</identifier><language>eng</language><publisher>Washington, DC: Elsevier Inc</publisher><subject>Antigen Presentation - immunology ; Biological and medical sciences ; Blood coagulation. Blood cells ; Cells, Cultured ; Coagulation factors ; Dendritic Cells - immunology ; Dendritic Cells - ultrastructure ; Endocytosis - immunology ; Factor VIII - immunology ; Fundamental and applied biological sciences. Psychology ; Humans ; Molecular and cellular biology ; T-Lymphocytes - immunology ; von Willebrand Factor - physiology</subject><ispartof>Blood, 2007-01, Vol.109 (2), p.610-612</ispartof><rights>2007 American Society of Hematology</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c456t-ef344ae430edb5b178ed8b638d7a11c3220f4cb747a2caa79437bb7ac998eb383</citedby><cites>FETCH-LOGICAL-c456t-ef344ae430edb5b178ed8b638d7a11c3220f4cb747a2caa79437bb7ac998eb383</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,27931,27932</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18439352$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16985172$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dasgupta, Suryasarathi</creatorcontrib><creatorcontrib>Repessé, Yohann</creatorcontrib><creatorcontrib>Bayry, Jagadeesh</creatorcontrib><creatorcontrib>Navarrete, Ana-Maria</creatorcontrib><creatorcontrib>Wootla, Bharath</creatorcontrib><creatorcontrib>Delignat, Sandrine</creatorcontrib><creatorcontrib>Irinopoulou, Theano</creatorcontrib><creatorcontrib>Kamaté, Caroline</creatorcontrib><creatorcontrib>Saint-Remy, Jean-Marie</creatorcontrib><creatorcontrib>Jacquemin, Marc</creatorcontrib><creatorcontrib>Lenting, Peter J.</creatorcontrib><creatorcontrib>Borel-Derlon, Annie</creatorcontrib><creatorcontrib>Kaveri, Srinivas V.</creatorcontrib><creatorcontrib>Lacroix-Desmazes, Sébastien</creatorcontrib><title>VWF protects FVIII from endocytosis by dendritic cells and subsequent presentation to immune effectors</title><title>Blood</title><addtitle>Blood</addtitle><description>Von Willebrand factor (VWF) is a chaperone molecule for procoagulant factor VIII (FVIII). Its role in the reduction of the immunogenicity of therapeutic FVIII in patients with hemophilia A has been evoked but lacks clear cellular and molecular rationale. Here, we demonstrate that VWF protects FVIII from being endocytosed by human dendritic cells (DCs) and subsequently presented to FVIII-specific T cells. The immunoprotective effect of VWF requires a physical interaction with FVIII because the endocytosis of FVIII was significantly restored on hindering the formation of the VWF-FVIII complex. Interestingly, VWF had no direct inhibitory effect either on the ability of DCs to present antigenic peptides or on the activation potency of CD4+ T cells. We thus propose that VWF may reduce the immunogenicity of FVIII by preventing, upstream from the activation of immune effectors, the entry of FVIII in professional antigen-presenting cells.</description><subject>Antigen Presentation - immunology</subject><subject>Biological and medical sciences</subject><subject>Blood coagulation. Blood cells</subject><subject>Cells, Cultured</subject><subject>Coagulation factors</subject><subject>Dendritic Cells - immunology</subject><subject>Dendritic Cells - ultrastructure</subject><subject>Endocytosis - immunology</subject><subject>Factor VIII - immunology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Molecular and cellular biology</subject><subject>T-Lymphocytes - immunology</subject><subject>von Willebrand Factor - physiology</subject><issn>0006-4971</issn><issn>1528-0020</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1r3DAQhkVoSbZp_0EpujQ3p_qyJV8KJXSbhUAvbXoU-hiDim2lGruw_75ydiG3ngahZ17eeQh5z9kt50Z88mPOsRGMdQ1rGyaEbrsLsuOtMA1jgr0iO7Z9ql7zK_IG8TdjXEnRXpIr3vWm5VrsyPD4a0-fSl4gLEj3j4fDgQ4lTxTmmMNxyZiQ-iON9V3SkgINMI5I3Rwprh7hzwrzUhMA63RLyjNdMk3TtM5AYRhqbi74lrwe3Ijw7jyvyc_91x93983D92-Huy8PTVBttzQwSKUcKMkg-tZzbSAa30kTteM8SCHYoILXSjsRnNO9ktp77ULfG_DSyGtyc8qtJ9VmuNgp4dbYzZBXtJ1RXHSKV1CdwFAyYoHBPpU0uXK0nNnNr332aze_lrX25LeufTjnr36C-LJ0FlqBj2fAYXDjUNwcEr5wRslethv3-cRBtfE3QbEYEswBYipVmY05_b_JP-71mug</recordid><startdate>20070115</startdate><enddate>20070115</enddate><creator>Dasgupta, Suryasarathi</creator><creator>Repessé, Yohann</creator><creator>Bayry, Jagadeesh</creator><creator>Navarrete, Ana-Maria</creator><creator>Wootla, Bharath</creator><creator>Delignat, Sandrine</creator><creator>Irinopoulou, Theano</creator><creator>Kamaté, Caroline</creator><creator>Saint-Remy, Jean-Marie</creator><creator>Jacquemin, Marc</creator><creator>Lenting, Peter J.</creator><creator>Borel-Derlon, Annie</creator><creator>Kaveri, Srinivas V.</creator><creator>Lacroix-Desmazes, Sébastien</creator><general>Elsevier Inc</general><general>The Americain Society of Hematology</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20070115</creationdate><title>VWF protects FVIII from endocytosis by dendritic cells and subsequent presentation to immune effectors</title><author>Dasgupta, Suryasarathi ; Repessé, Yohann ; Bayry, Jagadeesh ; Navarrete, Ana-Maria ; Wootla, Bharath ; Delignat, Sandrine ; Irinopoulou, Theano ; Kamaté, Caroline ; Saint-Remy, Jean-Marie ; Jacquemin, Marc ; Lenting, Peter J. ; Borel-Derlon, Annie ; Kaveri, Srinivas V. ; Lacroix-Desmazes, Sébastien</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c456t-ef344ae430edb5b178ed8b638d7a11c3220f4cb747a2caa79437bb7ac998eb383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Antigen Presentation - immunology</topic><topic>Biological and medical sciences</topic><topic>Blood coagulation. 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subjects | Antigen Presentation - immunology Biological and medical sciences Blood coagulation. Blood cells Cells, Cultured Coagulation factors Dendritic Cells - immunology Dendritic Cells - ultrastructure Endocytosis - immunology Factor VIII - immunology Fundamental and applied biological sciences. Psychology Humans Molecular and cellular biology T-Lymphocytes - immunology von Willebrand Factor - physiology |
title | VWF protects FVIII from endocytosis by dendritic cells and subsequent presentation to immune effectors |
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