Site-Specific Immunosuppression in Vascularized Composite Allotransplantation : Prospects and Potential

Skin is the most immunogenic component of a vascularized composite allograft (VCA) and is the primary trigger and target of rejection. The skin is directly accessible for visual monitoring of acute rejection (AR) and for directed biopsy, timely therapeutic intervention, and management of AR. Logical...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Clinical & developmental immunology 2013, Vol.2013 (2013), p.1-7
Hauptverfasser: Schnider, Jonas T., Weinstock, Matthias, Plock, Jan A., Solari, Mario G., Venkataramanan, Raman, Zheng, Xin Xiao, Gorantla, Vijay S.
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 7
container_issue 2013
container_start_page 1
container_title Clinical & developmental immunology
container_volume 2013
creator Schnider, Jonas T.
Weinstock, Matthias
Plock, Jan A.
Solari, Mario G.
Venkataramanan, Raman
Zheng, Xin Xiao
Gorantla, Vijay S.
description Skin is the most immunogenic component of a vascularized composite allograft (VCA) and is the primary trigger and target of rejection. The skin is directly accessible for visual monitoring of acute rejection (AR) and for directed biopsy, timely therapeutic intervention, and management of AR. Logically, antirejection drugs, biologics, or other agents delivered locally to the VCA may reduce the need for systemic immunosuppression with its adverse effects. Topical FK 506 (tacrolimus) and steroids have been used in clinical VCA as an adjunct to systemic therapy with unclear beneficial effects. However, there are no commercially available topical formulations for other widely used systemic immunosuppressive drugs such as mycophenolic acid, sirolimus, and everolimus. Investigating the site-specific therapeutic effects and efficacy of systemically active agents may enable optimizing the dosing, frequency, and duration of overall immunosuppression in VCA with minimization or elimination of long-term drug-related toxicity.
format Article
fullrecord <record><control><sourceid>emarefa</sourceid><recordid>TN_cdi_emarefa_primary_476208</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>476208</sourcerecordid><originalsourceid>FETCH-emarefa_primary_4762083</originalsourceid><addsrcrecordid>eNqFjMsKwjAURIMoWB-fIOQHCjGttrqTouiuUHFbLm0qkTQJuelCv94I4tbVHJgzMyLROktZzDcJG_-Y8ymZIT4YC7zLI3KvpBdxZUUjO9nQS98P2uBgrROI0mgqNb0BNoMCJ1-ipYXprcEwogeljHeg0SrQHvzH3tPSGQxvHinolpbGC-0lqAWZdKBQLL85J6vT8VqcY9GDEx3U1slAzzrNtpzlyb_-DWYLRh4</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Site-Specific Immunosuppression in Vascularized Composite Allotransplantation : Prospects and Potential</title><source>DOAJ Directory of Open Access Journals</source><source>PubMed Central</source><source>PubMed Central Open Access</source><creator>Schnider, Jonas T. ; Weinstock, Matthias ; Plock, Jan A. ; Solari, Mario G. ; Venkataramanan, Raman ; Zheng, Xin Xiao ; Gorantla, Vijay S.</creator><creatorcontrib>Schnider, Jonas T. ; Weinstock, Matthias ; Plock, Jan A. ; Solari, Mario G. ; Venkataramanan, Raman ; Zheng, Xin Xiao ; Gorantla, Vijay S.</creatorcontrib><description>Skin is the most immunogenic component of a vascularized composite allograft (VCA) and is the primary trigger and target of rejection. The skin is directly accessible for visual monitoring of acute rejection (AR) and for directed biopsy, timely therapeutic intervention, and management of AR. Logically, antirejection drugs, biologics, or other agents delivered locally to the VCA may reduce the need for systemic immunosuppression with its adverse effects. Topical FK 506 (tacrolimus) and steroids have been used in clinical VCA as an adjunct to systemic therapy with unclear beneficial effects. However, there are no commercially available topical formulations for other widely used systemic immunosuppressive drugs such as mycophenolic acid, sirolimus, and everolimus. Investigating the site-specific therapeutic effects and efficacy of systemically active agents may enable optimizing the dosing, frequency, and duration of overall immunosuppression in VCA with minimization or elimination of long-term drug-related toxicity.</description><identifier>ISSN: 1740-2522</identifier><identifier>EISSN: 1740-2530</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Puplishing Corporation</publisher><ispartof>Clinical &amp; developmental immunology, 2013, Vol.2013 (2013), p.1-7</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids></links><search><creatorcontrib>Schnider, Jonas T.</creatorcontrib><creatorcontrib>Weinstock, Matthias</creatorcontrib><creatorcontrib>Plock, Jan A.</creatorcontrib><creatorcontrib>Solari, Mario G.</creatorcontrib><creatorcontrib>Venkataramanan, Raman</creatorcontrib><creatorcontrib>Zheng, Xin Xiao</creatorcontrib><creatorcontrib>Gorantla, Vijay S.</creatorcontrib><title>Site-Specific Immunosuppression in Vascularized Composite Allotransplantation : Prospects and Potential</title><title>Clinical &amp; developmental immunology</title><description>Skin is the most immunogenic component of a vascularized composite allograft (VCA) and is the primary trigger and target of rejection. The skin is directly accessible for visual monitoring of acute rejection (AR) and for directed biopsy, timely therapeutic intervention, and management of AR. Logically, antirejection drugs, biologics, or other agents delivered locally to the VCA may reduce the need for systemic immunosuppression with its adverse effects. Topical FK 506 (tacrolimus) and steroids have been used in clinical VCA as an adjunct to systemic therapy with unclear beneficial effects. However, there are no commercially available topical formulations for other widely used systemic immunosuppressive drugs such as mycophenolic acid, sirolimus, and everolimus. Investigating the site-specific therapeutic effects and efficacy of systemically active agents may enable optimizing the dosing, frequency, and duration of overall immunosuppression in VCA with minimization or elimination of long-term drug-related toxicity.</description><issn>1740-2522</issn><issn>1740-2530</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqFjMsKwjAURIMoWB-fIOQHCjGttrqTouiuUHFbLm0qkTQJuelCv94I4tbVHJgzMyLROktZzDcJG_-Y8ymZIT4YC7zLI3KvpBdxZUUjO9nQS98P2uBgrROI0mgqNb0BNoMCJ1-ipYXprcEwogeljHeg0SrQHvzH3tPSGQxvHinolpbGC-0lqAWZdKBQLL85J6vT8VqcY9GDEx3U1slAzzrNtpzlyb_-DWYLRh4</recordid><startdate>2013</startdate><enddate>2013</enddate><creator>Schnider, Jonas T.</creator><creator>Weinstock, Matthias</creator><creator>Plock, Jan A.</creator><creator>Solari, Mario G.</creator><creator>Venkataramanan, Raman</creator><creator>Zheng, Xin Xiao</creator><creator>Gorantla, Vijay S.</creator><general>Hindawi Puplishing Corporation</general><scope>ADJCN</scope><scope>AHFXO</scope></search><sort><creationdate>2013</creationdate><title>Site-Specific Immunosuppression in Vascularized Composite Allotransplantation : Prospects and Potential</title><author>Schnider, Jonas T. ; Weinstock, Matthias ; Plock, Jan A. ; Solari, Mario G. ; Venkataramanan, Raman ; Zheng, Xin Xiao ; Gorantla, Vijay S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-emarefa_primary_4762083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Schnider, Jonas T.</creatorcontrib><creatorcontrib>Weinstock, Matthias</creatorcontrib><creatorcontrib>Plock, Jan A.</creatorcontrib><creatorcontrib>Solari, Mario G.</creatorcontrib><creatorcontrib>Venkataramanan, Raman</creatorcontrib><creatorcontrib>Zheng, Xin Xiao</creatorcontrib><creatorcontrib>Gorantla, Vijay S.</creatorcontrib><collection>الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals</collection><collection>معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete</collection><jtitle>Clinical &amp; developmental immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schnider, Jonas T.</au><au>Weinstock, Matthias</au><au>Plock, Jan A.</au><au>Solari, Mario G.</au><au>Venkataramanan, Raman</au><au>Zheng, Xin Xiao</au><au>Gorantla, Vijay S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Site-Specific Immunosuppression in Vascularized Composite Allotransplantation : Prospects and Potential</atitle><jtitle>Clinical &amp; developmental immunology</jtitle><date>2013</date><risdate>2013</risdate><volume>2013</volume><issue>2013</issue><spage>1</spage><epage>7</epage><pages>1-7</pages><issn>1740-2522</issn><eissn>1740-2530</eissn><abstract>Skin is the most immunogenic component of a vascularized composite allograft (VCA) and is the primary trigger and target of rejection. The skin is directly accessible for visual monitoring of acute rejection (AR) and for directed biopsy, timely therapeutic intervention, and management of AR. Logically, antirejection drugs, biologics, or other agents delivered locally to the VCA may reduce the need for systemic immunosuppression with its adverse effects. Topical FK 506 (tacrolimus) and steroids have been used in clinical VCA as an adjunct to systemic therapy with unclear beneficial effects. However, there are no commercially available topical formulations for other widely used systemic immunosuppressive drugs such as mycophenolic acid, sirolimus, and everolimus. Investigating the site-specific therapeutic effects and efficacy of systemically active agents may enable optimizing the dosing, frequency, and duration of overall immunosuppression in VCA with minimization or elimination of long-term drug-related toxicity.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Puplishing Corporation</pub><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1740-2522
ispartof Clinical & developmental immunology, 2013, Vol.2013 (2013), p.1-7
issn 1740-2522
1740-2530
language eng
recordid cdi_emarefa_primary_476208
source DOAJ Directory of Open Access Journals; PubMed Central; PubMed Central Open Access
title Site-Specific Immunosuppression in Vascularized Composite Allotransplantation : Prospects and Potential
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-19T02%3A56%3A36IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-emarefa&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Site-Specific%20Immunosuppression%20in%20Vascularized%20Composite%20Allotransplantation%20:%20Prospects%20and%20Potential&rft.jtitle=Clinical%20&%20developmental%20immunology&rft.au=Schnider,%20Jonas%20T.&rft.date=2013&rft.volume=2013&rft.issue=2013&rft.spage=1&rft.epage=7&rft.pages=1-7&rft.issn=1740-2522&rft.eissn=1740-2530&rft_id=info:doi/&rft_dat=%3Cemarefa%3E476208%3C/emarefa%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true