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 manage...

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Main Authors: Jonas T. Schnider, Matthias Weinstock, Jan A. Plock, Mario G. Solari, Raman Venkataramanan, Xin Xiao Zheng, Vijay S. Gorantla
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:Clinical and Developmental Immunology
Online Access:http://dx.doi.org/10.1155/2013/495212
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author Jonas T. Schnider
Matthias Weinstock
Jan A. Plock
Mario G. Solari
Raman Venkataramanan
Xin Xiao Zheng
Vijay S. Gorantla
author_facet Jonas T. Schnider
Matthias Weinstock
Jan A. Plock
Mario G. Solari
Raman Venkataramanan
Xin Xiao Zheng
Vijay S. Gorantla
author_sort Jonas T. Schnider
collection DOAJ
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.
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language English
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spelling doaj-art-e7d221f0cc844cc4a8d3b2def51ee4632025-02-03T07:24:49ZengWileyClinical and Developmental Immunology1740-25221740-25302013-01-01201310.1155/2013/495212495212Site-Specific Immunosuppression in Vascularized Composite Allotransplantation: Prospects and PotentialJonas T. Schnider0Matthias Weinstock1Jan A. Plock2Mario G. Solari3Raman Venkataramanan4Xin Xiao Zheng5Vijay S. Gorantla6Department of Plastic and Reconstructive Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USADepartment of Plastic and Reconstructive Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USADepartment of Plastic and Reconstructive Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USADepartment of Plastic and Reconstructive Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USADepartment of Pharmaceutical Sciences, University of Pittsburgh School of Pharmacy, Pittsburgh, PA 15261, USADepartment of Plastic and Reconstructive Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USADepartment of Plastic and Reconstructive Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USASkin 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.http://dx.doi.org/10.1155/2013/495212
spellingShingle Jonas T. Schnider
Matthias Weinstock
Jan A. Plock
Mario G. Solari
Raman Venkataramanan
Xin Xiao Zheng
Vijay S. Gorantla
Site-Specific Immunosuppression in Vascularized Composite Allotransplantation: Prospects and Potential
Clinical and Developmental Immunology
title Site-Specific Immunosuppression in Vascularized Composite Allotransplantation: Prospects and Potential
title_full Site-Specific Immunosuppression in Vascularized Composite Allotransplantation: Prospects and Potential
title_fullStr Site-Specific Immunosuppression in Vascularized Composite Allotransplantation: Prospects and Potential
title_full_unstemmed Site-Specific Immunosuppression in Vascularized Composite Allotransplantation: Prospects and Potential
title_short Site-Specific Immunosuppression in Vascularized Composite Allotransplantation: Prospects and Potential
title_sort site specific immunosuppression in vascularized composite allotransplantation prospects and potential
url http://dx.doi.org/10.1155/2013/495212
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